Page last updated: 2024-11-04

hydrochlorothiazide

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Description

Hydrochlorothiazide is a thiazide diuretic used to treat high blood pressure and fluid retention. It is synthesized through a multi-step process involving reactions with sulfuryl chloride, thiourea, and other reagents. Hydrochlorothiazide works by blocking the reabsorption of sodium and chloride ions in the kidneys, leading to increased urine production and a decrease in blood volume. It has been widely studied due to its effectiveness in managing hypertension, its long-term safety profile, and its relatively low cost. Hydrochlorothiazide is a cornerstone medication in the treatment of hypertension and is often used in combination with other antihypertensive drugs. Research continues to explore its potential in various medical conditions, including diabetes, kidney disease, and osteoporosis.'

Hydrochlorothiazide: A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hydrochlorothiazide : A benzothiadiazine that is 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide substituted by a chloro group at position 6 and a sulfonamide at 7. It is diuretic used for the treatment of hypertension and congestive heart failure. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

FloraRankFlora DefinitionFamilyFamily Definition
Aquariusgenus[no description available]AlismataceaeA plant family of the subclass ALISMATIDAE, class Liliopsida (monocotyledons) of aquatic plants. The flower parts are in threes with 3 green sepals and 3 white or yellow petals.[MeSH]

Cross-References

ID SourceID
PubMed CID5052
CHEMBL ID357497
CHEBI ID91839
SCHEMBL ID5372168
MeSH IDM0010703
PubMed CID3639
CHEMBL ID435
CHEBI ID5778
SCHEMBL ID9349
MeSH IDM0010703

Synonyms (688)

Synonym
HMS3269P15
BRD-A71765365-001-01-6
mepireserpate
nsc169414
1263-58-7
nsc-169414
yohimban-16-carboxylic acid, 11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-, methyl ester, (3.beta.,16.beta.,17.alpha.,18.beta.,20.alpha.)-
l -carpserp
roxynoid
resperine
serpentin
resiatric
eberspine
rolserp
serpil
sertensin
serpazil
sederaupin
reserpka
tenserpinie
rivased
serpyrit
tepserpine
tefaserpina
serpaneurona
serpedin
broserpine
hydromox r
hypercal b
seominal
ascoserp
hypertensan
brinderdin
terbolan
orthoserpina
tensional
renese r
abicol
tensanyl
rauserpin
salupres
veriloid
hydropres
adelfan
ebserpine
elfanex
neoslowten
methylreserpate 3,4,5-trimethoxybenzoic acid ester
adelphin
diupres
transerpin
perskleran
modenol
hypertane forte
briserine
alkaserp
salutensin
v-serp
supergan
raudixin
hexaplin
methyl reserpate 3,4,5-trimethoxybenzoate (ester)
darebon
serpilum
cardioserpin
pressimedin
banisil
methylreserpate 3,4,5-trimethoxybenzoic acid
tensionorme
diutensen-r
tylandril
solfo serpine
marnitension simple
butiserpazide-25
abesta
reserutin
idoserp
yohimban-16-carboxylic acid,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-, methyl ester, (16.beta.,17.alpha.,18.beta.,20.alpha.)-
nsc-80138
isoreserpin
20.alpha.-yohimban-16.beta.-carboxylic acid,17.alpha.-dimethoxy-, methyl ester, 3,4,5-trimethoxybenzoate (ester)
CHEMDIV1_007189
NCGC00142390-01
NCGC00142390-02
L000827
HMS607G17
methyl 11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16-carboxylate
AKOS004912845
CHEMBL357497
NCGC00015888-05
NCGC00015888-04
NCGC00015888-03
3,8-dimethoxy-4-(methoxycarbonyl)-1,2,3,4,5,11,14,14a,4a,5a-decahydrobenzo[3,4 -g]indolo[2,3-a]quinolizin-2-yl 3,4,5-trimethoxybenzoate
HMS3369J06
SCHEMBL5372168
component of regroton (salt/mix)
demi-regroton (salt/mix)
rauloycin
mio-pressin
benz(g)indolo(2,3-a)quinolizine-1-carboxylic acid, 1,2,3,4,4a,5,7,8,13,13b,14,14a-dodecahydro-3-hydroxy-2,11-dimethoxy-, methyl ester, 3,4,5-trimethoxybenzoate
component of salutensin (salt/mix)
adelphin-esidrex-k
methyl 11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16-carboxylate #
drenusil-r
QEVHRUUCFGRFIF-UHFFFAOYSA-N
neo-antitersol
serpentine 'pharbil'
3.beta.,20.alpha.-yohimban-16.beta.-carboxylic acid, 18.beta.-hydroxy-11,17.alpha.-dimethoxy- methyl ester 3,4,5-trimethoxybenzoate (ester)
component of renese r (salt/mix)
component of butiserpazide (salt/mix)
rauvilid
raunormin 'orzan'
serpatone
yohimban-16-carboxylic acid derivative of benz(g)indolo(2,3-a)quinolizine
serpasil-esidrex
component of diutensen-r (salt/mix)
component of naquival (salt/mix)
resomine
serplex k
component of metatensin (salt/mix)
sinesalin composition
serpresan
arcum r-s
unipres (salt/mix)
hydropres ka
serpasil-esidrex k
serp
methyl reserpate 3,4,5-trimethoxybenzoate
serpasil-esidrex no. 1
butiserpazide-50
tenserlix
seda-salurepin
serpasil apresoline
rauserpen-alk
tenserpine 'assia'
dypertane compound
reserpic acid methyl ester 3,4,5-trimethoxybenzoate
gamaserpin
resercrine
sarpagen
methyl 18.beta.-hydroxy-11,17.alpha.-dimethoxy-3.beta.,20.alpha.-yohimban-16.beta.-carboxylate 3,4,5-trimethoxybenzoate (ester)
hygroton-reserpine
methyl reserpate 3,4,5-trimethyloxybenzoic acid
component of diupres (salt/mix)
resersana
seda-recipin
butiserpine
nembu-serpin
tendoscen-compr.
resedin
3-.beta.,20-.alpha.-yohimban-16-.beta.-carboxylic acid, 18-.beta.-hydroxy-11,17-.alpha.-dimethoxy-,methyl ester, 3,4,5-trimethoxybenzoate
component of hydropres (salt/mix)
serpasil-esidrex no. 2
rauwiloid+
methyl (1r,15s,17r,18r,19s,20s)-6,18-dimethoxy-17-(3,4,5-trimethoxybenzoyl)oxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate
CHEBI:91839
yohimban-16-carboxylic acid, 11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-, methyl ester, (3beta,16beta,17alpha,18beta,20alpha)-
DTXSID30925499
FT-0674350
Q27163633
6,18-dimethoxy-17-[oxo-(3,4,5-trimethoxyphenyl)methoxy]-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylic acid methyl ester
AS-13241
methyl 6,18-dimethoxy-17-(3,4,5-trimethoxybenzoyl)oxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate
BIDD:GT0153
AB00052012-15
BRD-K13078532-001-05-2
2h-1,2,4-benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-, 1,1-dioxide
nci-c55925
component of esimil
hydril
hydrosaluric
jen-diril
thiuretic
hydrodiuretic
hidril
dihydrochlorothiazide
hydro-aquil
dihydrochlorothiazidum
component of butizide prestabs
hidrochlortiazid
thlaretic
hydrochlorthiazide
su 5879
component of dyazide
maschitt
idrotiazide
disalunil
hcz ,
dihydrochlorothiazid
aquarills
hypothiazid
wln: t66 bswm em dhj hg iszw
aquarius
3,2,4-benzothiadiazine-1,1-dioxide
6-chloro-7-sulfamoyl-3,2,4-benzothiadiazine 1,1-dioxide
6-chloro-3,2,4-benzothiadiazine 1,1-dioxide
3,4-dihydrochlorothiazide
dichlotiazid
6-chloro-3,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
nefrix
nsc53477
component of aldoril
hidrotiazida
hydro-diuril
oretic
hydrochlorothiazid
diclotride
vetidrex
2h-1,4-benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-, 1,1-dioxide
hypothiazide
megadiuril
hydrodiuril
chlorosulthiadil
dyazide
drenol
newtolide
dichlotride
hctz
esidrex
esidrix
nsc-53477
servithiazid
MLS000069619 ,
smr000035778
component of cyclex
DIVK1C_000289
KBIO1_000289
NCI60_004317
AF-614/30832002 ,
EU-0100614
hydrochlorothiazide, crystalline
prinzide
unipres
ser-ap-es
vaseretic
lotensin hct
SPECTRUM_000877
ziac
PRESTWICK_263
NCGC00015508-01
cas-58-93-5
NCGC00015508-02
lopac-h-4759
PRESTWICK2_000009
LOPAC0_000614
3,4-dihydro-6-chloro-7-sulfamyl-1,2, 4-benzothiadiazine-1,1-dioxide
6-chloro-3,4-dihydro-2h-1,2,4-benzothiadiazine-7-sulfonamide 1, 1-dioxide
6-chloro-7-sulfamoyl-3, 4-dihydro-2h-1,2,4-benzothiadiazine 1,1-dioxide
2h-1,2, 4-benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-, 1, 1-dioxide
6-chloro-1,1-dioxo-3,4-dihydro-2h-1$l^{6},2,4-benzothiadiazine-7-sulfonamide
6-chloro-3,4-dihydro-2h-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
6-chloro-3,4-dihydro-7-sulfamoyl-2h-1,2, 4-benzothiadiazine 1,1-dioxide
IDI1_000289
BSPBIO_002132
BPBIO1_000019
OPREA1_357174
BSPBIO_000017
SPECTRUM5_000824
h.h. 25/25
NCGC00021906-03
AB00052012
hydro-t
einecs 200-403-3
apo-hydro
hydrochlorothiazidum
hytrid
neo-minzil
nsc 53477
hydro par
hydrozide injection, veterinary
hct ,
hidrosaluretil
condiuren
catiazida
chlorsulfonamidodihydrobenzothiadiazine dioxide
dixidrasi
hydrochlorothiazidum [inn-latin]
dichlorosal
disothiazid
acesistem
aldazida
neo-flumen
bremil
dichlothiazide
6-chloro-3,4-dihydro-7-sulfamoyl-2h-1,2,4-benzothiadiazine 1,1-dioxide
hidroronol
cidrex
novodiurex
brn 0625101
clorana
hidroclorotiazida [inn-spanish]
hct-isis
panurin
aquazide h
aquazide-h
dihydran
chlorzide
hydro-saluric
mictrin
unazid
spironazide
ro-hydrazide
neoflumen
pantemon
thiaretic
microzide
mazide 25 mg
fluvin
natrinax
zide
diu 25 vigt
hydrochlorthiazidum
briazide
esoidrina
neo-codema
saldiuril
6-chloro-3,4-dihydro-7-sulfamoyl-2h-1,2,4-benzothiadiazine-1,1-dioxide
hydrothide
acuilix
2h-1,2,4-benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-, 1, 1-dioxide
diurogen
hydro-d
3,4-dihydro-6-chloro-7-sulfamoyl-1,2,4-benzothiadiazine-1,1-dioxide
urodiazin
urozide
raunova plus
ivaugan
inderide
hidro-niagrin
concor plus
h.h. 50/50
chlorizide
medozide
hyclosid
selozide
diaqua
6-chloro-3,4-dihydro-2h-1,2,4-benzothiadiazine-7-sulfonamide-1,1-dioxide
tandiur
hsdb 3096
diu-melusin
modurcen
6-chloro-7-sulfamoyl-3,4-dihydro-2h-1,2,4-benzothiadiazine 1,1-dioxide
hydrocot
caplaril
aldectazide 50/50
chlothia
didral
idroclorotiazide [dcit]
3,4-dihydro-6-chloro-7-sulfamyl-1,2,4-benzothiadiazine-1,1-dioxide
carozide
hydrochlorothiazide intensol
ccris 2082
nefrol
manuril
timolide
mikorten
direma
indroclor
hydrozide
aldactazide 25/25
inderide 80/25
STK315354
58-93-5
C07041
hydrochlorothiazide
component of aldactazide
component of caplaril
hydrochlorothiazide, meets usp testing specifications
DB00999
hydrochlorothiazide (jp17/usp/inn)
microzide (tn)
esidrix (tn)
D00340
PRESTWICK3_000009
NCGC00021906-06
NCGC00021906-08
NCGC00021906-05
moduretic
maxzide
apresazide
aldactazide
KBIOGR_000351
KBIO3_001352
KBIOSS_001357
KBIO2_003925
KBIO2_001357
KBIO2_006493
MAYBRIDGE1_004336
PRESTWICK0_000009
NINDS_000289
PRESTWICK1_000009
SPBIO_001938
SPECTRUM4_000006
SPECTRUM3_000456
SPBIO_001259
SPECTRUM2_001040
SPECTRUM1500335
NCGC00015508-03
NCGC00021906-07
NCGC00021906-04
lopressor hct
aquazide
bmcl182567 compound 6a
bdbm13076
jfd00715
cid_3639
NCGC00015508-07
HMS2091L05
H 4759 ,
7-(aminosulfonyl)-6-chloro-3,4-dihydro-(2h)-1,2,4-benzothiadiazine 1,1-dioxide
6-chloro-7-sulfamoyl-3,4-dihydro-(2h)-1,2,4-benzothiadiazine 1,1-dioxide
6-chloro-3,4-dihydro-(2h)-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
H1274
NCGC00015508-12
HMS553N04
6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-dioxide
copalia-hct
hydrochlorothiaizide
dafiro-hct
chebi:5778 ,
dihydrochlorurite
su-5879
exforge-hct
CHEMBL435
imprida-hct
rasilez-hct
HMS500O11
FT-0650564
HMS1920D19
HMS1568A19
NCGC00015508-08
AKOS000121373
A19550
HMS3259O17
HMS3261L10
HMS2095A19
NCGC00259114-01
NCGC00254017-01
tox21_300292
tox21_201565
nsc-757059
pharmakon1600-01500335
nsc757059
dtxsid2020713 ,
tox21_110165
dtxcid80713
HMS2235I09
CCG-40240
NCGC00015508-09
NCGC00015508-04
NCGC00015508-11
NCGC00015508-14
NCGC00015508-13
NCGC00015508-05
NCGC00015508-10
NCGC00015508-06
dihydrochlorurit
dihydroxychlorothiazidum
ezide
0j48lph2th ,
hydrex-semi
acuretic
hidroclorotiazida
idroclorotiazide
unii-0j48lph2th
hydrochlorot
hydrochlorat
hydrochlorothiazide [usp:inn:ban:jan]
NCGC00015508-17
LP00614
hydrochlorothiazide component of hydro-ride
hydrochlorothiazide component of vaseretic
hydrochlorothiazide component of zestoretic
kervezide component hydrochlorothiazide
zestoretic component hydrochlorothiazide
aldactazide component hydrochlorothiazide
hydrochlorothiazide component of hydrap-es
hydrochlorothiazide component of riprazo
hydrochlorothiazide component of aldactazide
exforge hct component hydrochlorothiazide
lotensin hct component hydrochlorothiazide
hydrochlorothiazide component of rasitrio
esimil component hydrochlorothiazide
aldoril component hydrochlorothiazide
lopressor hct component hydrochlorothiazide
hydrochlorothiazide [inn]
hydrochlorothiazide [vandf]
hydrochlorothiazide component of normozide
ibersartan/hydrochlorothiazide zentiva component hydrochlorothiazide
hydrochlorothiazide [orange book]
hydrochlorothiazide component of irbesartan/hydrochlorothiazide teva
hydrochlorothiazide component of rasilez-hct
hydrochlorothiazide component of monopril hct
hydrochlorothiazide component of sprimeo-hct
sprimeo-hct component hydrochlorothiazide
oreticyl forte component hydrochlorothiazide
hydrochlorothiazide [ep monograph]
hydrochlorothiazide component of teveten hct
hydrochlorothiazidum [who-ip latin]
hydrochlorothiazide component of kinzalkomb
hydrochlorothiazide component of hydropres
tolucombi component hydrochlorothiazide
teveten hct component hydrochlorothiazide
hydrochlorothiazide component of hydra-zide
unipres component hydrochlorothiazide
hydrochlorothiazide component of cam-ap-es
hydro-reserp component hydrochlorothiazide
hydrochlorothiazide component of benicar hct
hydrochlorothiazide [usp-rs]
uniretic component hydrochlorothiazide
hydrochlorothiazide [green book]
prinzide component hydrochlorothiazide
hydrochlorothiazide component of lopressor hct
benicar hct component hydrochlorothiazide
h.r.-50 component hydrochlorothiazide
hydrochlorothiazide component of dyazide
hydrap-es component hydrochlorothiazide
hydrochlorothiazide component of micardisplus
hydrochlorothiazide component
tekturna hct component hydrochlorothiazide
hydrochlorothiazde component of toulomi
vaseretic component hydrochlorothiazide
hydrochlorothiazide component of maxzide
rasitrio component hydrochlorothiazide
hydro-ride component hydrochlorothiazide
ser-a-gen component hydrochlorothiazide
hydrochlorothiazide component of irbesartan/hydrochlorothiazide-bms
micardis hct component hydrochlorothiazide
hydrochlorothiazide component of esimil
hydrochlorothiazide component of prinzide
irbesartan/hydrochlorothiazide-bms component hydrochlorothiazide
dyazide component hydrochlorothiazide
monopril hct component hydrochlorothiazide
hydrochlorothiazide component of moduretic
cam-ap-es component hydrochlorothiazide
hydrochlorothiazide component of viskazide
hydrochlorothiazide component of apresazide
hydrochlorothiazide component of dutoprol
hydrochlorothiazide component of exforge hct
hyzaar component hydrochlorothiazide
apresoline-esidrix component hydrochlorothiazide
hydrochlorothiazide component of ziac
hydrochlorothiazide component of quinaretic
hydroserpine plus (r-h-h) component hydrochlorothiazide
hydrochlorothiazide [who-ip]
diovan hct component hydrochlorothiazide
hydrochlorothiazide [jan]
normozide component hydrochlorothiazide
ziac component hydrochlorothiazide
hydrochlorothiazide component of ibersartan/hydrochlorothiazide zentiva
moduretic component hydrochlorothiazide
hydrochlorothiazide component of lotensin hct
serpasil-esidrix component hydrochlorothiazide
hydrochlorothiazide [ema epar]
hydrochlorothiazide component of micardis hct
hydrochlorothiazide component of avalide
hydrochlorothiazide component of serpasil-esidrix
hydrochlorothiazide component of ser-a-gen
quinaretic component hydrochlorothiazide
hydrochlorothiazide component of unipres
riprazo component hydrochlorothiazide
hydra-zide component hydrochlorothiazide
hydrochlorothiazide [who-dd]
hydrochlorothiazide [mart.]
ifirmacombi component hydrochlorothiazide
viskazide component hydrochlorothiazide
micardisplus component hydrochlorothiazide
ser-ap-es component hydrochlorothiazide
hydrochlorothiazide component of tribenzor
hydrochlorothiazide component of hydro-reserp
amturnide component hydrochlorothiazide
maxzide component hydrochlorothiazide
hydrochlorothiazide component of tekturna hct
hydralazine hydrochloride-hydrochlorothiazide-reserpine component hydrochlorothiazide
8049-49-8
hydrochlorothiazide component of oreticyl forte
hydrochlorothiazide component of diovan hct
kinzalkomb component hydrochlorothiazide
accuretic component hydrochlorothiazide
tribenzor component hydrochlorothiazide
apresazide component hydrochlorothiazide
hydrochlorothiazide [usp monograph]
hydrochlorothiazide component of hyzaar
hydrochlorothiazide component of ser-ap-es
hydrochlorothiazide component of apresoline-esidrix
hydrochlorothiazide [hsdb]
hydrochlorothiazide component of aldoril
hh-50/50
hydrochlorothiazide component of uniretic
hydrochlorothiazide [iarc]
hydrochlorothiazide component of hydroserpine plus (r-h-h)
hydrochlorothiazide component of h.r.-50
hydrochlorothiazide component of amturnide
hydrochlorothiazide component of ifirmacombi
avalide component hydrochlorothiazide
dutoprol component hydrochlorothiazide
hydropres component hydrochlorothiazide
hydrochlorothiazide [ep impurity]
pritorplus component hydrochlorothiazide
irbesartan/hydrochlorothiazide teva component hydrochlorothiazide
hydrochlorothiazide component of hydralazine hydrochloride-hydrochlorothiazide-reserpine
hydrochlorothiazide [mi]
S1708
gtpl4836
HMS3370P11
HY-B0252
NC00510
SCHEMBL9349
tox21_110165_1
NCGC00015508-16
tox21_500614
NCGC00261299-01
6-chloro-1,1-dioxo-3,4-dihydro-2h-1lambda6,2,4-benzothiadiazine-7-sulfonamide
PS-3162
6-chloro-3,4-dihydro-1,1-dioxo-7-sulfamoyl-1,2,4-benzothiadiazine
Q-201210
component of butizide prestabs (salt/mix)
manschitt
thiazide, hydrochloro-
aldoril (salt/mix)
prinzide (salt/mix)
6-chloro-7-sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine-1,1-dioxide
component of caplaril (salt/mix)
urirex
6-chloro-7-sulfamoyl-3,4-dihydrobenzo-1,2,4-thiadiazine-1,1-dioxide
2h-1,2,4-benzothiadiazine, 6-chloro-3,4-dihydro-7-sulfamoyl-2, 1,1-dioxide
hyzaar (salt/mix)
inderide (salt/mix)
idrodiuvis
hydrochlorzide
hydropres (salt/mix)
tekturna hct (salt/mix)
dutoprol (salt/mix)
component of dyazide (salt/mix)
accuretic (salt/mix)
6-chloro-3,4-dihydro-2h-benzo[e][1,2,4]thiadiazine-7-sulfonamide 1,1-dioxide
HMS3428A05
AB00052012_16
AB00052012_17
OPERA_ID_168
mfcd00051765
Z56347248
AC-8114
sr-01000000119
SR-01000000119-2
hydrochlorothiazide, united states pharmacopeia (usp) reference standard
hydrochlorothiazide, drug standard, 1.0 mg/ml in methanol
hydrochlorothiazide, european pharmacopoeia (ep) reference standard
HMS3655M21
hydrochloro thiazide
hydrochlorothiazide, pharmaceutical secondary standard; certified reference material
hydrochlorothiazide for peak identification, european pharmacopoeia (ep) reference standard
hydrochlorothiazide 1.0 mg/ml in methanol
hypothiazide (c7h8cln3o4s2)
SR-01000000119-4
SR-01000000119-6
SBI-0050596.P004
HMS3712A19
hydrochlorothiazide, british pharmacopoeia (bp) reference standard
6-chloro-1,1-dioxo-1,2,3,4-tetrahydro-1lambda~6~,2,4-benzothiadiazine-7-sulfonamide
SW196569-3
BCP22001
Q423930
hydropar
hydrokraft
125727-50-6
6-chloro-3,4-dihydro-2h-1,2,4-benzothiadiazine-7-sulphonamide-1,1-dioxide
6-chloro-1,1-dioxo-3,4-dihydro-2h-1$l^{6,2,4-benzothiadiazine-7-sulfonamide
SDCCGSBI-0050596.P005
2h-1,2,4-benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-,1,1-dioxide
NCGC00015508-25
6-chloro-1,1-dioxo-3,4-dihydro-2h-1,2,4-benzothiadiazine-7-sulfonamide
H10742
hydrochlorothiazide form ii
BH164522
EN300-16641
hydrochlorothiazide (usp monograph)
hydrochlorothiazide (iarc)
hydrochlorothiazide (mart.)
hydrochlorothiazide (ep monograph)
hydrochlorothiazidum (inn-latin)
6-chloro-3,4-dihydro-2h-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
hidroclorotiazida (inn-spanish)
panurin dichlotride
hydrochlorothiazide (usp-rs)
hydrochlorothiazide (ep impurity)
hydrochlorothiazide (usp:inn:ban:jan)
c03aa03

Research Excerpts

Overview

Hydrochlorothiazide (HCTZ) is a thiazide diuretic used for the treatment of hypertension and edema associated with noncardiogenic pulmonary edema. The long action (>4 h) dosage form is lacking in the commercial market and development of modified-release formulation may have industrial significance.

ExcerptReferenceRelevance
"Hydrochlorothiazide (HCTZ) is a frequently prescribed diuretic that exhibits photosensitizing properties. "( Does systemic hydrochlorothiazide increase the risk of developing ultraviolet radiation-induced skin tumours in hairless mice?
Al-Chaer, RN; Lerche, CM; Wulf, HC, 2023
)
2.71
"Hydrochlorothiazide (HCTZ) is a recommended drug for the prevention of heart disease, but its long action (>4 h) dosage form is lacking in the commercial market and development of modified-release formulation may have industrial significance."( Employment of Quality by Design Approach via Response Surface Methodology to Optimize and Develop Modified-release Formulation of Hydrochlorothiazide.
Maheshwari, R; Paliwal, S; Sharma, S; Singhai, VD, 2021
)
1.55
"Hydrochlorothiazide (HCTZ) is a thiazide diuretic used in adults and children for the treatment of hypertension and edema. "( Pharmacokinetics of Hydrochlorothiazide in Children: A Potential Surrogate for Renal Secretion Maturation.
Al-Uzri, A; Boakye-Agyeman, F; Cohen-Wolkowiez, M; Commander, SJ; Harper, B; Hornik, CD; Hornik, CP; Melloni, C; Mendley, SR; Wu, H; Zimmerman, K, 2021
)
2.39
"Hydrochlorothiazide (HCZ) is a BCS Class IV drug with low solubility and low permeability. "( Natural Plus Synthetic Hydrotropic Solubilization using Response Surface Methodology to Optimize the Solid Dispersion of Hydrochlorothiazide.
Nainwal, N; Saharawat, A, 2022
)
2.37
"Hydrochlorothiazide (HTZ) is a first-line drug used in the treatment of hypertension suffered from low oral bioavailability due to poor aqueous solubility and permeability. "( Egg White Protein Carrier-Assisted Development of Solid Dispersion for Improved Aqueous Solubility and Permeability of Poorly Water Soluble Hydrochlorothiazide.
Jain, SP; Kharkar, PS; Pethe, AM; Telange, DR, 2021
)
2.27
"Hydrochlorothiazide (HCTZ) is a commonly prescribed sulfonamide thiazide-type diuretic medication that has been associated with rare cases of noncardiogenic pulmonary edema."( Recurrent Hydrochlorothiazide-Induced Acute Respiratory Distress Syndrome Treated With Extracorporeal Membrane Oxygenation.
Jansson, PS; Lee, J; Leisten, DC; Sarkisian, TM; Wilcox, SR, 2018
)
2.33
"Hydrochlorothiazide (HCTZ) is a thiazide diuretic used for the treatment of hypertension and edema associated with fluid overload conditions such as congestive heart failure (CHF). "( Population-based meta-analysis of hydrochlorothiazide pharmacokinetics.
Mager, DE; Mallikaarjun, S; Shoaf, SE; Van Wart, SA, 2013
)
2.11
"Hydrochlorothiazide is a diuretic used to treat hypertension that belongs to class IV of the Biopharmaceutics Classification System. "( Quality evaluation of pharmaceutical formulations containing hydrochlorothiazide.
de Oliveira, MA; Silva, DC; Yoshida, MI, 2014
)
2.09
"Hydrochlorothiazide (HCT) is a diuretic and a BCS class IV drug with low solubility and low permeability, exhibiting poor oral absorption. "( Cocrystals of Hydrochlorothiazide: Solubility and Diffusion/Permeability Enhancements through Drug-Coformer Interactions.
Clara, D; Desiraju, GR; Devi, VK; Ganguly, S; Malviya, N; Sanphui, P, 2015
)
2.22
"Hydrochlorothiazide is a thiazide diuretic widely used in clinics to treat arterial hypertension. "( Inclusion complexes of hydrochlorothiazide and β-cyclodextrin: Physicochemical characteristics, in vitro and in vivo studies.
Buttchevitz, A; de Oliveira Benedet, P; Kratz, JM; Kruger, JH; Mendes, C; Oliveira, PR; Silva, MA; Simões, CM, 2016
)
2.19
"Hydrochlorothiazide is a widely used antihypertensive agent and one of its major impurities, salamide (4-amino-6-chlorobenzene-1,3-disulphonamide), has a chemical structure containing a primary amino group, a functional group that has previously been reported to be associated with carcinogenic activity. "( An investigation of the mutagenic activity of salamide - a major impurity of hydrochlorothiazide.
Bostanci, O; Cok, I; Emerce, E; Sari, S, 2016
)
2.11
"Hydrochlorothiazide (HCT) is a diuretic used to treat hypertension. "( Development and validation of a reversed-phase high-performance liquid chromatographic method with solid-phase extraction for the quantification of hydrochlorothiazide in ex vivo permeation studies.
Granero, GE; Longhi, MR; Onnainty, R; Quevedo, MA; Schenfeld, EM, 2017
)
2.1
"Hydrochlorothiazide (HCTZ) is a class IV drug according to the Biopharmaceutical Classification System. "( Self-Nanoemulsified Drug Delivery System of Hydrochlorothiazide for Increasing Dissolution Rate and Diuretic Activity.
Buttchevitz, A; Caon, T; de Oliveira Benedet, P; Kruger, JH; Lemos-Senna, E; Mendes, C; Silva, MAS, 2017
)
2.16
"Hydrochlorothiazide (HCTZ) is a sulfonamide-containing drug with commonly reported adverse effects that include electrolyte abnormalities, orthostatic hypotension, hyperglycemia, and photosensitivity. "( Severe allergic reaction to hydrochlorothiazide mimicking septic shock.
Cheng, EY; Mineo, MC, 2009
)
2.09
"Hydrochlorothiazide is a common diuretic antihypertensive drug of the thiazide family. "( Pharmaceutical composition of hydrochlorothiazide:β-cyclo-dextrin: preparation by three different methods, physico-chemical characterization and in vivo diuretic activity evaluation.
Pires, MA; Sinisterra, RD; Souza Dos Santos, RA, 2011
)
2.1
"Hydrochlorothiazide at low dose is a frequent component of such biotherapies: it is efficacious and secure."( [Kinzalkomb, a fixed telmisartan-hydrochlorothiazide combination for the treatment of hypertension].
Kulbertus, H, 2003
)
1.32
"Hydrochlorothiazide (HCT) is a well-established diuretic and antihypertensive agent, which promotes natruresis by acting on the distal renal tubule."( Metoprolol succinate extended release/hydrochlorothiazide combination tablets.
Hainer, JW; Sugg, J, 2007
)
1.33

Effects

Hydrochlorothiazide (HCT) has been suggested to induce photosensitivity, thereby increasing the incidence of skin cancers. HCTZ has been shown to reduce urine volume in nephrogenic diabetes insipidus.

ExcerptReferenceRelevance
"But hydrochlorothiazide has an FI value of 4.09 with relatively large fluctuating concentrations."( Pharmacokinetics of the combined preparation of lisinopril and hydrochlorothiazide on Chinese healthy volunteers.
Sun, DL; Sun, YY; Wang, KS; Wei, Y; Zheng, MY, 2011
)
1.09
"Hydrochlorothiazide (HCT) has been suggested to induce photosensitivity, thereby increasing the incidence of skin cancers. "( Association of hydrochlorothiazide treatment compared with alternative diuretics with overall and skin cancer risk: a propensity-matched cohort study.
Böhm, M; Götzinger, F; Hardtstock, F; Krieger, J; Kunz, M; Lauder, L; Mahfoud, F; Maywald, U; Schulz, M; Wilke, T, 2023
)
2.71
"Hydrochlorothiazide (HCTZ) use has been linked to skin cancer in northern European countries. "( Use of hydrochlorothiazide and risk of skin cancer in a large nested case-control study in Spain.
Díaz, Y; Duarte-Salles, T; Huerta, C; León-Muñoz, LM; Llorente, A; Montero-Corominas, D; Pottegård, A; Puente, D, 2021
)
2.52
"Hydrochlorothiazide has been shown to cause rare, but serious non-cardiogenic pulmonary edema. "( Life-threatening idiopathic reaction to hydrochlorothiazide treated with veno-venous extracorporeal membrane oxygenation.
Cohen, E; Kane, SP, 2018
)
2.19
"Hydrochlorothiazide use has been associated with markedly increased risk for squamous cell carcinoma. "( Hydrochlorothiazide use and risk for Merkel cell carcinoma and malignant adnexal skin tumors: A nationwide case-control study.
Friis, S; Gaist, D; Hölmich, LR; Johannesdottir Schmidt, SA; Pedersen, SA; Pottegård, A, 2019
)
3.4
"Hydrochlorothiazide (HCTZ) has been shown to reduce urine volume in nephrogenic diabetes insipidus, raising the possibility that HCTZ could also be effective in reducing tolvaptan-induced polyuria."( Hydrochlorothiazide ameliorates polyuria caused by tolvaptan treatment of polycystic kidney disease in PCK rats.
Hirose, T; Ito, S; Kinugasa, S; Mori, T; Muroya, Y; Oba-Yabana, I; Ohsaki, Y; Sato, E; Takahashi, C; Wang, A, 2019
)
2.68
"Hydrochlorothiazide has been recognized to cause subacute cutaneous lupus erythematosus, but very few cases of systemic drug induced lupus systemic erythematosus have been reported."( When Chest Pain Reveals More: A Case of Hydrochlorothiazide-Induced Systemic Lupus Erythematosus.
Brahmamdam, R; Girnita, D; Pasula, S; Sosenko, T, 2019
)
1.5
"Hydrochlorothiazide (HCTZ) has often been contrasted with chlorthalidone, but relatively little is known about HCTZ versus indapamide (INDAP). "( Head-to-head comparisons of hydrochlorothiazide with indapamide and chlorthalidone: antihypertensive and metabolic effects.
Ernst, ME; Kostis, JB; Roush, GC; Sica, DA; Tandon, S, 2015
)
2.15
"Hydrochlorothiazide has less effect on blood pressure, a high risk of metabolic side effects, and may not have pleiotropic effects."( [All diuretics used in the treatment of hypertension are not the same].
Asil, S; Atalar, E, 2017
)
1.18
"Hydrochlorothiazide (HCTZ) has become by far the most commonly prescribed antihypertensive drug in the US. "( Half a century of hydrochlorothiazide: facts, fads, fiction, and follies.
Bangalore, S; Messerli, FH, 2011
)
2.15
"But hydrochlorothiazide has an FI value of 4.09 with relatively large fluctuating concentrations."( Pharmacokinetics of the combined preparation of lisinopril and hydrochlorothiazide on Chinese healthy volunteers.
Sun, DL; Sun, YY; Wang, KS; Wei, Y; Zheng, MY, 2011
)
1.09
"Hydrochlorothiazide (HCTZ) has not been shown to reduce mortality or cardiovascular events when given as a single agent. "( Hydrochlorothiazide: is it a wise choice?
DiNicolantonio, JJ, 2012
)
3.26
"Hydrochlorothiazide has been shown to exert direct vasodilator effects by activation of calcium-activated potassium (KCa) channels in human and guinea pig isolated resistance arteries. "( Inhibition of carbonic anhydrase accounts for the direct vascular effects of hydrochlorothiazide.
Garcha, RS; Hughes, AD; Pickkers, P; Schachter, M; Smits, P, 1999
)
1.97
"The hydrochlorothiazide test has been adopted as official first action and added to Table 36:05."( Microcrystalline identification test of some amphetamines and hydrochlorothiazide: collaborative study.
Auerbach, L, 1978
)
0.98
"Hydrochlorothiazide has been found to be highly effective in preventing recurrence of calcium stones in our personal experience with over 300 patients who have been treated for as long as 14 years with this agent."( The management of the patient with calcium stones.
Cohanim, M; Yendt, ER, 1976
)
0.98

Actions

Hydrochlorothiazide (HCTZ) promotes sodium excretion, resulting in a reduction of plasma volume. Lisinopril tended to decrease whole blood viscosity at all shear rates.

ExcerptReferenceRelevance
"Hydrochlorothiazide (HCTZ) promotes sodium excretion, resulting in a reduction of plasma volume and peripheral resistance."( Pharmacokinetic properties and bioequivalence of olmesartan medoxomil/hydrochlorothiazide in healthy Korean male subjects.
Chae, SW; Choi, Y; Im, YJ; Jeon, JY; Jin, C; Jung, JA; Kim, MG; Kim, Y; Park, K, 2014
)
1.36
"4. Hydrochlorothiazide caused an increase in urinary sodium excretion only on the first day of treatment."( The antidiuretic effect of chronic hydrochlorothiazide treatment in rats with diabetes insipidus: water and electrolyte balance.
Laycock, JF; Shirley, DG; Skinner, J; Walter, SJ, 1982
)
1.06
"Hydrochlorothiazide tended to increase and lisinopril tended to decrease whole blood viscosity at all shear rates but these changes did not reach statistical significance."( Effects of lisinopril and hydrochlorothiazide on platelet function and blood rheology in essential hypertension: a randomly allocated double-blind study.
Bray-Desboscs, L; Donner, M; el Ghawi, R; Stoltz, JF; Thibout, E; Zannad, F, 1993
)
1.31
"Hydrochlorothiazide did not produce a statistically significant increase in urinary amylase excretion but did reduce the ratio of salivary amylase/creatinine clearance in a two-hour urine collection."( The influence of hydrochlorothiazide and tripamide on serum and urinary amylase.
Conrad, KA; Fagan, TC; Simons, JA, 1988
)
1.34

Treatment

Treatment with hydrochlorothiazide (50 mg/day) produced a decline in fasting urinary Ca. Treatment was associated with hypokalemia, which was not present in losartan or indapamide treatment. Hydrochlorothsiazide treatment was slightly more effective than indomethacin treatment in reducing the urine volume and increasing the urine osmolality.

ExcerptReferenceRelevance
"Hydrochlorothiazide treatment significantly reduced the BP in all 92 patients (62 males, aged 45·7 ± 9·6 years), irrespective of their baseline BP subtypes. "( Hypertension subtypes modify metabolic response to thiazide diuretics.
Chen, JW; Huang, CC; Huang, PH; Leu, HB; Lin, LY; Lin, SJ; Wu, TC, 2016
)
1.88
"Hydrochlorothiazide treatment was associated with hypokalemia, which was not present in losartan or indapamide treatment."( Comparative study of hydrochlorothiazide and indapamide on the anti-atherogenic potential of losartan in cholesterol fed rat.
Islam, MZ; Rahman, MS, 2010
)
1.4
"Hydrochlorothiazide treatment was slightly more effective than indomethacin treatment in reducing the urine volume and increasing the urine osmolality."( Response to indomethacin and hydrochlorothiazide in nephrogenic diabetes insipidus.
Jonkman, A; Monnens, L; Thomas, C, 1984
)
1.28
"Hydrochlorothiazide treatment decreased diastolic blood pressure to 83.1 +/- 5.6 mm Hg, and MAP to 101.1 +/- 6.5 mm Hg."( Assessment of blood pressure during treatment with naproxen or ibuprofen in hypertensive patients treated with hydrochlorothiazide.
Goodfriend, TL; Klassen, D; Peterson, CA; Schuna, AA; Young, DY, 1993
)
1.22
"Hydrochlorothiazide treatment in hypercalciuric and osteoporotic men was associated with a rapid rebound increase in bone mineral density."( Rapid recovery of bone mass in hypercalciuric, osteoporotic men treated with hydrochlorothiazide.
Adams, JS; Kantorovich, V; Song, CF, 1999
)
1.97
"Hydrochlorothiazide treatment increased plasma renin activity twofold but did not change kidney cortical renin mRNA, COX-2 mRNA, or COX-2 immunoreactivity."( Furosemide stimulates macula densa cyclooxygenase-2 expression in rats.
Hartner, A; Jensen, BL; Kammerl, M; Krämer, BK; Kurtz, A; Mann, B, 2001
)
1.03
"Hydrochlorothiazide treatment did not prevent the hyperuricemia or arteriolopathy despite controlling blood pressure."( Hyperuricemia induces a primary renal arteriolopathy in rats by a blood pressure-independent mechanism.
Chen, Q; Feng, L; Gordon, KL; Han, L; Johnson, RJ; Kanellis, J; Kang, DH; Lan, HY; Mazzali, M; Nakagawa, T; Watanabe, S; Xia, YY, 2002
)
1.04
"Hydrochlorothiazide treatment caused potassium loss and an increase in the levels of uric acid and triglycerides."( Comparison of fosinopril and hydrochlorothiazide in patients with mild to moderate hypertension.
Backman, R; Forslund, T; Franzén, P, 1991
)
1.29
"Hydrochlorothiazide treatment was accompanied by a decrease in serum potassium and an increase in serum uric acid."( The efficacy and tolerability of long-term felodipine treatment in hypertension. The Scandinavian Multicenter Group.
Ibsen, H; Westberg, B, 1990
)
1
"Hydrochlorothiazide treatment compared with vehicle treatment did not ameliorate any index of renal function but resulted in significant elevations in plasma urea and creatinine levels."( Effect of 8-phenyltheophylline, enprofylline and hydrochlorothiazide on glycerol-induced acute renal failure in the rat.
Bowmer, CJ; Collis, MG; Kellett, R; Yates, MS, 1987
)
1.25
"More hydrochlorothiazide-treated patients developed abnormalities in the levels of serum glucose, uric acid, blood urea nitrogen (BUN), serum potassium, and chloride."( Comparative hypotensive effects of acebutolol and hydrochlorothiazide in patients with mild to moderate essential hypertension: a double-blind multicenter evaluation.
Singh, BN; Thoden, WR; Wahl, J, 1986
)
0.98
"Hydrochlorothiazide and binazine treatment decreased systolic and diastolic blood pressure, the total electromechanical systolic time index (QS2I) and the left ventricular ejection time index (LVETI), and increased the PEP/LVET index at rest and after exercise."( Post-exertion changes in left ventricular systolic time intervals in patients with primary hypertension treated with hydrochlorothiazide, binazine, and propranolol.
Cholewa, M; Górski, L; Markiewicz, K, 1985
)
1.2
"Treatment with hydrochlorothiazide 12.5 to 50 mg/d led to a decrease in mean levels of urine calcium (427 ± 174 mg/d to 251 ± 114 mg/d; P < 0.001) and parathyroid hormone (115 ± 57 ng/L to 74 ± 36 ng/L; P < 0.001), with no change in serum calcium level (10.7 ± 0.4 mg/dL off treatment, 10.5 ± 1.2 mg/dL on treatment, P = 0.4)."( Thiazide Treatment in Primary Hyperparathyroidism-A New Indication for an Old Medication?
Benbassat, C; Diker-Cohen, T; Gorshtein, A; Herzberg, D; Hirsch, D; Masri-Iraqi, H; Shimon, I; Shochat, T; Shraga-Slutzky, I; Tsvetov, G, 2017
)
0.79
"Treatment with hydrochlorothiazide diminished the delipidation rate value whereas propranolol mildly increased the removal rate of the remnant particle."( Effects of hydrochlorothiazide and propranolol treatment on chylomicron metabolism in hypertensive objects.
Bernik, MM; Cazita, PM; Heimann, JC; Nakandakare, ER; Neves, MQ; Nunes, VS; Quintão, EC; Rocha, JC, 2005
)
1.06
"Treatment with hydrochlorothiazide or chlorpropamide orally gave inadequate antidiuresis, but response to injections of vasopressin tannate in oil was sufficient for satisfactory management."( Idiopathic neurogenic diabetes insipidus in a cat.
Court, MH; Watson, AD, 1983
)
0.61
"Treatment with hydrochlorothiazide controlled his hyperkalemia and hypertension."( Pseudohypoaldosteronism: case report and discussion of the syndrome.
Bia, MJ; Throckmorton, DC,
)
0.47
"Treatment with hydrochlorothiazide or enalapril resulted in a lowering of systolic and diastolic blood pressures, but diastolic pressure was lower in patients treated with enalapril (89 +/- 2 and 82 +/- 2 mm Hg, respectively; p less than 0.05)."( Effects of hydrochlorothiazide, diltiazem and enalapril on mononuclear cell sodium and magnesium levels in systemic hypertension.
Abraham, AS; Barchilon, E; Brooks, BA; Eylath, U; Grafstein, Y; Nubani, N; Shemesh, O, 1991
)
1.01
"Treatment with hydrochlorothiazide also lowered blood pressure but had no significant effect on left ventricular weight to body weight ratio [2.54(0.04)]."( Effects of antihypertensive drugs on heart and resistance vessels.
Fouad-Tarazi, FM; Kobayashi, H; Sano, T; Tarazi, RC, 1990
)
0.62
"Treatment with hydrochlorothiazide resulted in a significant increase in mean ouabain-sensitive ATPase activity (+/- SEM) from 118.4 +/- 14.6 to 158.1 +/- 15.3 nmol phosphate released per milligram of protein (P = 0.0004)."( Effect of treatment with hydrochlorothiazide on the red cell Na,K-adenosine triphosphatase in men with hypertension.
Del Greco, F; Finn, M; Quintanilla, AP; Weffer, MI, 1987
)
0.92
"Treatment with hydrochlorothiazide is effective in patients without increased urinary excretion of prostaglandin, whereas patients with increased prostaglandin excretion respond better to indomethacin therapy."( [Clinical variants of idiopathic hypercalciuria in children].
Bachmann, H; Kohout, I, 1987
)
0.61
"Treatment with hydrochlorothiazide (50 mg/day) produced a decline in fasting urinary Ca (to 0.07 +/- 0.02 mg/100 ml GF; P less than 0.01), serum PTH (from 39 +/- 19 to 21 +/- 1 microliters eq/ml; P less than 0.05), and urinary cAMP excretion (from 5.30 +/- 0.57 to 3.57 +/- 0.59 nmol/100 ml GF; P less than 0.0025)."( Postmenopausal osteoporosis as a manifestation of renal hypercalciuria with secondary hyperparathyroidism.
Glass, K; Nicar, MJ; Pak, CY; Sakhaee, K, 1985
)
0.61

Toxicity

ClorOTIC is the first large-scale trial to evaluate whether the addition of a thiazide diuretic (hydrochlorothiazide) to a loop diuret would improve blood pressure control.

ExcerptReferenceRelevance
" Overall, adverse reactions characterized as probably drug-related or questinably drug-related were reported in 28% of patients treated with tienilic acid, 24% treated with hydrochlorothiazide, 25% of patients treated with probenecid and 33% treated with placebo."( Safety of tienilic acid.
Beg, MA; Ragland, R, 1979
)
0.45
" In clinical trials, adverse experiences in patients treated with a lisinopril-hydrochlorothiazide combination were dizziness (7."( Review of international safety data for lisinopril-hydrochlorothiazide combination treatment.
Murray, NH, 1991
)
0.76
" Adverse events were reported in 11 of the 38 patients in the ramipril group, in 22 of 83 patients treated with the combination for more than 50 weeks, and in 9 of 38 patients treated with the combination for 50 weeks or less."( Efficacy and safety of ramipril in combination with hydrochlorothiazide: results of a long-term study.
Bauer, B; Breitstadt, A; Cairns, V; Froer, KL; Heidbreder, D, 1991
)
0.53
" Adverse events were those to be expected with these classes of drug and were reported in 48 (26."( A double-blind comparison of the efficacy and safety of lacidipine and hydrochlorothiazide in essential hypertension. The Southern Italy Lacidipine Study Group.
Chiariello, M, 1991
)
0.51
"Carvedilol has been shown to be effective and safe in patients with essential hypertension when given as monotherapy."( Safety and antihypertensive efficacy of carvedilol and atenolol alone and in combination with hydrochlorothiazide.
Hörrmann, M; Machwirth, M; van der Does, R; Widmann, L, 1990
)
0.5
" Nine patients experienced adverse events during combination treatment."( The safety of adding carvedilol to hypertensive patients inadequately treated with diuretics.
Dupont, AG; Schoors, DF; Venuti, RP, 1990
)
0.28
" Thus amlodipine administered once daily is an effective and safe agent for second-step therapy in mild to moderate essential hypertension."( Safety and efficacy of amlodipine added to hydrochlorothiazide therapy in essential hypertension.
Chrysant, SG; Glasser, SP; Graves, J; Koehn, DK; Rofman, B, 1989
)
0.54
" Three patients required drug discontinuation because of adverse effects."( Efficacy and safety of nitrendipine in patients with severe hypertension: a multiclinic study.
Jain, AK; Maronde, R; McMahon, FG; Mroczek, W; Ryan, JR; Vlachakis, N, 1984
)
0.27
" Enalapril has a good safety profile as measured by frequency of clinical and laboratory adverse experiences."( The efficacy and safety of enalapril in moderate to severe essential hypertension.
Kramsch, DM; Kulaga, SF; Walker, JF, 1984
)
0.27
" The achievement of normotensive blood pressure levels was accompanied by a decrease in the number of adverse effects reported."( Safety and efficacy of a three-drug regimen for the treatment of hypertension: hydrochlorothiazide, propranolol, and guanadrel.
Gore, RD, 1983
)
0.49
" Clonidine caused adverse effects more frequently than did lofexidine."( Comparative efficacy and safety of lofexidine and clonidine in mild to moderately severe systemic hypertension.
Lopez, LM; Mehta, JL, 1984
)
0.27
" Hypokalemia was the most frequently reported adverse reaction."( Clinical efficacy and safety of indapamide in the treatment of edema.
Slotkoff, L, 1983
)
0.27
" Withdrawals owing to adverse events were three from trandolapril and eight from the captopril group."( Comparison of the efficacy and safety of trandolapril and captopril for 16 weeks in mild-to-moderate essential hypertension. Investigator Study Group.
Pauly, NC; Safar, ME, 1994
)
0.29
" The incidence of adverse events was similar in all three groups."( Double-blind comparison of the efficacy and safety of trandolapril 2 mg and hydrochlorothiazide 25 mg in patients with mild-to-moderate essential hypertension. Investigator Study Group.
Meyer, BH; Pauly, NC, 1994
)
0.52
" Thus, the no observed adverse effect level (NOAEL) for both maternal and developmental toxicity was 3000 mg/kg/day."( The evaluation of the developmental toxicity of hydrochlorothiazide in mice and rats.
George, JD; Kimmel, CA; Marr, MC; Price, CJ; Tyl, RW, 1995
)
0.55
" The incidence of adverse events, particularly cough, was lower with benazepril + hydrochlorothiazide than with benazepril alone; no notable changes in body weight or heart rate were seen in either group."( Efficacy and safety of benazepril plus hydrochlorothiazide versus benazepril alone in hypertensive patients unresponsive to benazepril monotherapy.
Holwerda, K; Hoogma, RP; Huige, RC; Oldenbroek, C; Rijnierse, JM; Wester, A,
)
0.63
"1%) were the clinical adverse experiences most often reported in patients treated with losartan."( Safety and tolerability of losartan potassium, an angiotensin II receptor antagonist, compared with hydrochlorothiazide, atenolol, felodipine ER, and angiotensin-converting enzyme inhibitors for the treatment of systemic hypertension.
Dunlay, MC; Goldberg, AI; Sweet, CS, 1995
)
0.51
" The incidence of adverse events was lower in the combination group than in either of the monotherapy groups, and there were no serious clinically significant laboratory abnormalities in the combination group."( Study of the efficacy and safety of the combination ramipril 2.5 mg plus hydrochlorothiazide 12.5 mg in patients with mild-to-moderate hypertension. ATHES Study Group.
Genthon, R, 1994
)
0.52
" Based on the results obtained in these trials, both dose combinations of Fos/HCTZ taken once daily were safe and effective in the management of patients with mild-to-moderate hypertension."( Efficacy and safety of fosinopril/hydrochlorothiazide combinations on ambulatory blood pressure profiles in hypertension. Fosinopril/Hydrochlorothiazide Investigators.
Battikha, JP; Guthrie, R; Plesher, MM; Reggi, DR; Saini, RK, 1996
)
0.57
"5) represents a safe drug without relevant side effects or gross toxicity."( Preclinical safety studies of the combination moexipril hydrochloride/hydrochlorothiazide.
Friehe, H; Gietl, R; Ney, P, 1998
)
0.53
"Concern based on the reported short-term adverse effects of antihypertensive agents on plasma lipid and lipoprotein profiles (PLPPs) has complicated the therapy for hypertension."( Diuretics and beta-blockers do not have adverse effects at 1 year on plasma lipid and lipoprotein profiles in men with hypertension. Department of Veterans Affairs Cooperative Study Group on Antihypertensive Agents.
Cushman, WC; Freis, ED; Lakshman, MR; Materson, BJ; Reda, DJ, 1999
)
0.3
" Patients achieving positive DBP control using hydrochlorothiazide (responders) showed no adverse changes in PLPPs, whereas nonresponders exhibited increases in triglycerides, total cholesterol, and low-density lipoprotein cholesterol levels."( Diuretics and beta-blockers do not have adverse effects at 1 year on plasma lipid and lipoprotein profiles in men with hypertension. Department of Veterans Affairs Cooperative Study Group on Antihypertensive Agents.
Cushman, WC; Freis, ED; Lakshman, MR; Materson, BJ; Reda, DJ, 1999
)
0.56
"None of these 6 antihypertensive drugs has any long-term adverse effects on PLPPs and, therefore, may be safely prescribed."( Diuretics and beta-blockers do not have adverse effects at 1 year on plasma lipid and lipoprotein profiles in men with hypertension. Department of Veterans Affairs Cooperative Study Group on Antihypertensive Agents.
Cushman, WC; Freis, ED; Lakshman, MR; Materson, BJ; Reda, DJ, 1999
)
0.3
" Eprosartan was well tolerated; the overall incidence of adverse events was comparable to that in the enalapril group."( Efficacy and safety of eprosartan in severe hypertension. Eprosartan Multinational Study Group.
Sega, R, 1999
)
0.3
"Treatment of hypertensive patients with fixed-dose combination therapy consisting of losartan and hydrochlorothiazide (HCTZ) has several potential benefits over monotherapy with each of the individual components: more effective blood pressure control, a reduction in the likelihood of adverse effects, and facilitation of patients staying on therapy due to a simple once-daily regimen."( Safe and effective management of hypertension with fixed-dose combination therapy: focus on losartan plus hydrochlorothiazide.
Benedict, CR,
)
0.56
" Overall adverse events for bisoprolol and amlodipine were 39% and 40%, respectively."( Efficacy, safety, and effects on quality of life of bisoprolol/hydrochlorothiazide versus amlodipine in elderly patients with systolic hypertension.
Benetos, A; Consoli, S; Dubanchet, A; Safar, M; Safavian, A, 2000
)
0.55
" Drug-related adverse experiences occurred in 30 patients (22."( Efficacy and safety of losartan/hydrochlorothiazide in patients with severe hypertension.
Aurup, P; Goldberg, A; Oparil, S; Snavely, D, 2001
)
0.59
"Control of hypertension is hindered by the incidence of adverse events associated with therapy, which can result in low patient compliance."( Eprosartan provides safe and effective long-term maintenance of blood pressure control in patients with mild to moderate essential hypertension.
Levine, B, 2001
)
0.31
" Adverse events, serious adverse events, and discontinuations attributed to adverse events were infrequent."( Efficacy and safety of omapatrilat with hydrochlorothiazide for the treatment of hypertension in subjects nonresponsive to hydrochlorothiazide alone.
Barbosa, JA; Ferdinand, K; Kushnir, E; Lewin, A; Saini, R; Yellen, L, 2001
)
0.58
" Safety was assessed by determining the incidence of clinical and laboratory Adverse events and evaluating mean changes in pulse, body weight, electrocardiographic parameters, and laboratory test results."( Antihypertensive efficacy and safety of losartan alone and in combination with hydrochlorothiazide in adult African Americans with mild to moderate hypertension.
Alderman, M; Alexander, J; Ceesay, P; Espenshade, M; Flack, JM; Goldberg, A; Gradman, A; Green, S; Kraus, WE; Lester, FM; Pratt, JH; Saunders, E; Vargas, R, 2001
)
0.54
" The incidence of clinical adverse events was comparable in the 3 treatment groups."( Antihypertensive efficacy and safety of losartan alone and in combination with hydrochlorothiazide in adult African Americans with mild to moderate hypertension.
Alderman, M; Alexander, J; Ceesay, P; Espenshade, M; Flack, JM; Goldberg, A; Gradman, A; Green, S; Kraus, WE; Lester, FM; Pratt, JH; Saunders, E; Vargas, R, 2001
)
0.54
" Thus, combination therapy of losartan/hydrochlorothiazide seems useful in the treatment of elderly hypertension, showing additive BP lowering effect without metabolic adverse effects."( [Efficacy and safety of combination therapy with losartan and hydrochlorothiazide in elderly hypertension].
Abe, I; Eto, K; Iida, M; Tsuchihashi, T, 2002
)
0.82
"The ideal antihypertensive drug should be effective in reducing blood pressure, but have a low incidence of adverse effects."( Safety and tolerability of eprosartan in combination with hydrochlorothiazide.
Böhm, M; Sachse, A, 2002
)
0.56
" Most adverse events were of mild-to-moderate intensity and unrelated to treatment."( Long-term exposure to telmisartan as monotherapy or combination therapy: efficacy and safety.
Freytag, F; Holwerda, NJ; Karlberg, BE; Meinicke, TW; Schumacher, H, 2002
)
0.31
" Safety was assessed in both studies by the incidence of adverse experiences."( Pharmacokinetics, safety, and antihypertensive efficacy of losartan in combination with hydrochlorothiazide in hypertensive patients with renal impairment.
Dickson, TZ; Lin, CC; Lo, MW; Ramjit, D; Ritter, MA; Shahinfar, S; Snavely, D; Zagrobelny, J, 2003
)
0.54
" Incidence and severity of adverse events and physical examination and laboratory parameters were monitored for the safety evaluation."( Angiotensin II receptor antagonist telmisartan in isolated systolic hypertension (ARAMIS) study: efficacy and safety of telmisartan 20, 40 or 80 mg versus hydrochlorothiazide 12.5 mg or placebo.
de Zeeuw, D; Köster, J; Manolis, AJ; Murphy, MB; Reid, JL; Seewaldt-Becker, E, 2004
)
0.52
" All-causality adverse events occurred in 19."( Angiotensin II receptor antagonist telmisartan in isolated systolic hypertension (ARAMIS) study: efficacy and safety of telmisartan 20, 40 or 80 mg versus hydrochlorothiazide 12.5 mg or placebo.
de Zeeuw, D; Köster, J; Manolis, AJ; Murphy, MB; Reid, JL; Seewaldt-Becker, E, 2004
)
0.52
"3%) in the enalapril group experienced adverse events that were judged related to treatment."( Efficacy and safety of delapril plus manidipine compared with enalapril plus hydrochlorothiazide in mild to moderate essential hypertension: results of a randomized trial.
Cremonesi, G; Dobovisek, J; Fogari, R; Mugellini, A; Planinc, D, 2004
)
0.55
" Tolerability and safety were assessed by physical examination, laboratory parameters and evaluation of adverse events."( Assessment of efficacy, safety and tolerability of fixed dose combination of telmisartan 40mg and hydrochlorothiazide 12.5mg in adult Indian patients with mild to moderate hypertension.
Chandrasekharan, S; Desai, A; Ganesan, R; Gawde, A; Jain, SD; Jayaram, S; Kadam, GS; Lahoti, S; Mishra, AB; Muralidharan, RS; Rajadhyaksha, GC; Sodhi, SS, 2004
)
0.54
" Although considered safe and effective, their use is associated with dyslipidemia, hyperglycemia, and an increased risk of developing type 2 diabetes."( Demographic, environmental, and genetic predictors of metabolic side effects of hydrochlorothiazide treatment in hypertensive subjects.
Boerwinkle, E; Chapman, AB; Klungel, OH; Maitland-van der Zee, AH; Schwartz, GL; Turner, ST, 2005
)
0.56
" The incidence of adverse events during both phases was comparably low and the results of laboratory tests were unremarkable."( Efficacy and safety of combination therapy using high- or low-dose hydrochlorothiazide with valsartan or other Angiotensin-receptor blockers.
Ansari, A; Fuenfstueck, R; Hempel, RD; Klebs, S; Weidinger, G,
)
0.37
"5 million adverse drug reaction (ADR) reports for 8620 drugs/biologics that are listed for 1191 Coding Symbols for Thesaurus of Adverse Reaction (COSTAR) terms of adverse effects."( Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
Benz, RD; Contrera, JF; Kruhlak, NL; Matthews, EJ; Weaver, JL, 2004
)
0.32
" There were no significant differences in the incidences of clinical and laboratory drug-related adverse events between any of the combination groups and the placebo group."( Antihypertensive efficacy and safety of fixed-dose combination therapy with losartan plus hydrochlorothiazide in Japanese patients with essential hypertension.
Hirayama, Y; Matsuoka, H; Nonaka, K; Ogihara, T; Saruta, T; Suzuki, H; Takahashi, K; Toki, M, 2007
)
0.56
" Treatment was well tolerated in all three-treatment groups with a slight increase in adverse events in the combination therapy group."( A comparison of the efficacy and safety of irbesartan/HCTZ combination therapy with irbesartan and HCTZ monotherapy in the treatment of moderate hypertension.
Bhaumik, A; Franklin, SS; Lapuerta, P; Neutel, JM; Ptaszynska, A, 2008
)
0.35
" The main adverse event related to Felodipine was headache, and to Lisinopril was cough."( [Efficacy, safety and tolerance of Felodipine controlled release tablets and Felodipine controlled release tablets associated combination therapy in the treatment of mild to moderate essential hypertension in China].
Chen, YY; Liu, HL; Shen, FR; Sun, NL; Tao, J; Wu, HY; Xiang, XP; Yu, ZQ; Zhang, FC; Zhang, L; Zhang, WZ; Zhao, JA, 2007
)
0.34
" Overall adverse event rates were similar with aliskiren (61."( Comparative efficacy and safety of aliskiren, an oral direct renin inhibitor, and ramipril in hypertension: a 6-month, randomized, double-blind trial.
Ali, MA; Andersen, K; Constance, CM; Egan, B; Jin, J; Keefe, DL; Weinberger, MH, 2008
)
0.35
" Combination therapy was generally well-tolerated; the most commonly reported adverse events were headache (7."( Long-term safety, tolerability and efficacy of aliskiren in combination with valsartan in patients with hypertension: a 6-month interim analysis.
Chrysant, SG; Dattani, D; Hoppe, UC; Hsu, H; Murray, AV; Patel, S; Zhang, J, 2008
)
0.35
" The incidence and causality of all adverse events (AEs) and laboratory abnormalities occurring during treatment were recorded."( The safety profile of telmisartan as monotherapy or combined with hydrochlorothiazide: a retrospective analysis of 50 studies.
Mancia, G; Schumacher, H, 2008
)
0.58
" The most frequent suspected adverse reactions were dizziness and headache, which were comparable across groups and studies."( The safety profile of telmisartan as monotherapy or combined with hydrochlorothiazide: a retrospective analysis of 50 studies.
Mancia, G; Schumacher, H, 2008
)
0.58
" Adverse event rates were similar with aliskiren- (65."( Long-term antihypertensive efficacy and safety of the oral direct renin inhibitor aliskiren: a 12-month randomized, double-blind comparator trial with hydrochlorothiazide.
Botha, J; Gorostidi, M; Guerediaga, J; Maboudian, M; Philipp, T; Schmieder, RE; Smith, B; van Ingen, H; Weissbach, N, 2009
)
0.55
" T80/H25 FDC was well tolerated; drug-related adverse events occurred in 29 (4."( Long-term, open-label evaluation of the safety and efficacy of telmisartan 80 mg/hydrochlorothiazide 25 mg fixed-dose combination alone or with other antihypertensive medication.
Edwards, C; Neldam, S, 2009
)
0.58
" Main outcome parameters were the systolic (SBP) and diastolic (DBP) blood pressure reduction, the rate of normalized patients at study end compared to baseline, and the number and type of adverse events (AEs)."( Efficacy and safety of losartan 100 mg or losartan 100 mg plus hydrochlorothiazide 25 mg in the treatment of patients with essential arterial hypertension and CV risk factors: observational, prospective study in primary care.
Bestehorn, K; Bönner, G; Jung, C; Smolka, W, 2009
)
0.59
" Between-group comparisons of adverse events and changes in laboratory parameters did not reach statistical significance, except for uric acid which showed a significant increase in the valsartan/hydrochlorothiazide group compared with the amlodipine group, but was still below the laboratory's upper limit of normal."( Efficacy and safety of valsartan/hydrochlorothiazide fixed-dose combination compared with amlodipine monotherapy as first-line therapy for mild to moderate hypertension.
Chao, CL; Chen, JC; Chiang, FT; Hwang, JJ; Lin, LC; Lin, LY; Lin, YH; Tsai, CT; Wang, YC,
)
0.6
" The incidence of treatment-related adverse events (AEs) was similar with combination and monotherapy (11."( Safety and tolerability of fixed-dose irbesartan/hydrochlorothiazide for rapid control of severe hypertension.
Bhaumik, A; Franklin, SS; Lapuerta, P; Neutel, JM; Oparil, S, 2009
)
0.61
" Clinical and laboratory adverse events were reported for 29 patients (11%), but serious abnormalities were not observed."( One-year effectiveness and safety of open-label losartan/hydrochlorothiazide combination therapy in Japanese patients with hypertension uncontrolled with ARBs or ACE inhibitors.
Ayabe, T; Eto, T; Etoh, T; Ichiki, Y; Kato, J; Kita, T; Kitamura, K; Tamaki, N; Yokota, N, 2010
)
0.61
"One of the reasons for suboptimal blood pressure (BP) control in patients with hypertension is poor adherence to treatment, which may be caused by treatment-emergent adverse events."( Safety and tolerability of an olmesartan medoxomil-based regimen in patients with stage 1 hypertension: a randomized, double-blind, placebo-controlled study.
Chrysant, SG, 2010
)
0.36
"In patients with stage 1 hypertension, the olmesartan medoxomil-based regimen was generally well tolerated at all titration steps, and discontinuation due to adverse events was similar between olmesartan medoxomil and placebo."( Safety and tolerability of an olmesartan medoxomil-based regimen in patients with stage 1 hypertension: a randomized, double-blind, placebo-controlled study.
Chrysant, SG, 2010
)
0.36
" This regimen was also effective in terms of BP lowering and enabling patients to achieve BP goals without an adverse effect on tolerability."( Safety and tolerability of an olmesartan medoxomil-based regimen in patients with stage 1 hypertension: a randomized, double-blind, placebo-controlled study.
Chrysant, SG, 2010
)
0.36
" An understanding of structure-activity relationships (SARs) of chemicals can make a significant contribution to the identification of potential toxic effects early in the drug development process and aid in avoiding such problems."( Developing structure-activity relationships for the prediction of hepatotoxicity.
Fisk, L; Greene, N; Naven, RT; Note, RR; Patel, ML; Pelletier, DJ, 2010
)
0.36
" Safety was assessed by monitoring and recording adverse events (AEs)."( Long-term safety and efficacy of aliskiren and valsartan combination with or without the addition of HCT in patients with hypertension.
Chrysant, SG; Dattani, D; Hoppe, UC; Murray, AV; Patel, S; Ritter, S; Zhang, J, 2010
)
0.36
" Moreover, combination therapy comprising OM plus hydrochlorothiazide can significantly increase BP goal achievement without significantly increasing adverse events."( Efficacy and safety of olmesartan medoxomil in patients with stage 1 hypertension: blood pressure lowering and goal achievement.
Wilford Germino, F, 2010
)
0.61
" Adverse events were experienced by 34."( Efficacy and safety of aliskiren-based dual and triple combination therapies in US minority patients with stage 2 hypertension.
Ferdinand, KC; Israel, M; Jaimes, EA; Lee, J; Purkayastha, D; Weitzman, R,
)
0.13
"In this multicenter, multicountry study including 7567 Asian patients with hypertension, valsartan/hydrochlorothiazide single pill combination was found efficacious, well tolerated, and devoid of any serious adverse effects."( Efficacy, safety, and tolerability of valsartan/hydrochlorothiazide in Asian patients with essential hypertension.
Dongre, N; Lai, WT; Park, JE; Wang, J, 2011
)
0.84
" Treatment-emergent adverse event rates were similar between treatment groups regardless of the presence of diabetes or body mass index (BMI) status."( A comparison of the efficacy and safety of irbesartan/hydrochlorothiazide combination therapy with irbesartan monotherapy in the treatment of moderate or severe hypertension in diabetic and obese hypertensive patients: a post-hoc analysis review.
Neutel, JM, 2011
)
0.62
" Most treatment-emergent adverse events were mild to moderate in severity."( Efficacy and safety of triple-combination therapy with olmesartan, amlodipine, and hydrochlorothiazide in study participants with hypertension and diabetes: a subpopulation analysis of the TRINITY study.
Chrysant, SG; Fernandez, V; Heyrman, R; Izzo, JL; Kereiakes, DJ; Lee, J; Littlejohn, T; Melino, M; Oparil, S,
)
0.36
" Aliskiren, with or without add-on HCTZ, was generally well tolerated; the incidence of adverse events (AEs) during the core study was similar among the four final treatment groups."( Long-term safety and tolerability of the oral direct renin inhibitor aliskiren with optional add-on hydrochlorothiazide in patients with hypertension: a randomized, open-label, parallel-group, multicentre, dose-escalation study with an extension phase.
Gradman, AH; Keefe, DL; Kolloch, RE; Lederballe, O; Sica, D; Zhang, J, 2011
)
0.59
" Since these adverse effects did not disappear after the return to Preminent(®) at the end of Stage C, we performed an additional 3-month follow-up (extended stage)."( Comparison of the efficacy and safety of single-pill fixed-dose combinations of losartan/hydrochlorothiazide and valsartan/hydrochlorothiazide in patients with hypertension (SALT-VAT study).
Inoue, A; Kuwano, T; Mitsutake, R; Miura, S; Morii, J; Saku, K; Shiga, Y; Uehara, Y, 2011
)
0.59
"Single-pill fixed-dose combination therapy using Preminent(®) showed significant 24-h BP-lowering effects and was safe when compared with CodioMD(®)."( Comparison of the efficacy and safety of single-pill fixed-dose combinations of losartan/hydrochlorothiazide and valsartan/hydrochlorothiazide in patients with hypertension (SALT-VAT study).
Inoue, A; Kuwano, T; Mitsutake, R; Miura, S; Morii, J; Saku, K; Shiga, Y; Uehara, Y, 2011
)
0.59
"Antihypertensive therapy is effective in reducing the risk of major adverse cardiovascular events."( Combination of amlodipine plus angiotensin receptor blocker or diuretics in high-risk hypertensive patients: a 96-week efficacy and safety study.
Deng, Q; Liu, L; Liu, M; Ma, L; Sun, H; Wang, J; Wang, W; Zhang, Y; Zhao, Y, 2012
)
0.38
" Safety evaluations included monitoring of any adverse events (AEs)."( Combination of amlodipine plus angiotensin receptor blocker or diuretics in high-risk hypertensive patients: a 96-week efficacy and safety study.
Deng, Q; Liu, L; Liu, M; Ma, L; Sun, H; Wang, J; Wang, W; Zhang, Y; Zhao, Y, 2012
)
0.38
" Serious adverse events were more frequent in E (2."( Efficacy and safety of early versus late titration of fixed-dose irbesartan/hydrochlorothiazide: ACTUAL study.
Aoun, J; Girerd, X; Rosenbaum, D, 2011
)
0.6
" Although blood levels of potassium, hemoglobin A1c and uric acid (UA) significantly increased after 3 months for all of the patients, none of the patients showed serious adverse effects."( Efficacy and safety of a single-pill fixed-dose combination of high-dose telmisartan/hydrochlorothiazide in patients with uncontrolled hypertension.
Arimura, T; Fujisawa, K; Inoue, A; Kuwano, T; Matsunaga, E; Mitsutake, R; Miura, S; Morii, J; Nagata, I; Norimatsu, K; Saku, K; Shiga, Y; Shimizu, T; Shirotani, T; Uehara, Y, 2012
)
0.6
" A low dose of HCTZ in combination with candesartan reduces blood pressure effectively without adverse effects on the glucose and lipid profiles."( Low dose of hydrochlorothiazide, in combination with angiotensin receptor blocker, reduces blood pressure effectively without adverse effect on glucose and lipid profiles.
Fujiwara, W; Ishii, J; Izawa, H; Kinoshita, K; Morimoto, S; Mukaide, D; Nomura, M; Ozaki, Y; Ukai, G; Yokoi, H, 2013
)
0.77
" Metabolic parameters maintained a limited range of changes after 3 years, and adverse events were markedly decreased after 1-year treatment."( Three-year safety and effectiveness of fixed-dose losartan/hydrochlorothiazide combination therapy in Japanese patients with hypertension under clinical setting (PALM-1 Extension Study).
Ayabe, T; Eto, T; Etoh, T; Ichiki, Y; Kato, J; Kita, T; Kitamura, K; Tamaki, N; Yokota, N, 2012
)
0.62
" There were no significant differences in adverse effects between groups, with the exception of more respiratory disorders in the amlodipine/benazepril group than in the valsartan/hydrochlorothiazide group (17 vs 5; P = 0 ."( Comparison of the efficacy and safety profiles of two fixed-dose combinations of antihypertensive agents, amlodipine/benazepril versus valsartan/hydrochlorothiazide, in patients with type 2 diabetes mellitus and hypertension: a 16-week, multicenter, rando
Chen, JF; Hung, YJ; Lee, IT; Lee, WJ; Sheu, WH; Wang, CY, 2012
)
0.77
" However, respiratory adverse events (particularly coughing) were more frequently reported in the amlodipine/benazepril group."( Comparison of the efficacy and safety profiles of two fixed-dose combinations of antihypertensive agents, amlodipine/benazepril versus valsartan/hydrochlorothiazide, in patients with type 2 diabetes mellitus and hypertension: a 16-week, multicenter, rando
Chen, JF; Hung, YJ; Lee, IT; Lee, WJ; Sheu, WH; Wang, CY, 2012
)
0.58
" At least one adverse event occurred in 141 (1."( [Effectiveness and safety of losartan and its combination with hydrochlorothiazide in patients with hypertension: in result study].
Glezer, MG; Saĭgitov, RT, 2012
)
0.62
" Safety was assessed by recording all adverse events."( Safety and efficacy of aliskiren/amlodipine/hydrochlorothiazide triple combination in patients with moderate to severe hypertension: a 54-week, open-label study.
Garcia-Puig, J; Koenig, W; Murray, AV; Patel, S; Uddin, A; Zhang, J, 2012
)
0.64
"0%) reported a serious adverse event."( Efficacy and safety of a fixed combination of irbesartan/hydrochlorothiazide in Chinese patients with moderate to severe hypertension.
Dai, QY; Huang, QF; Li, Y; Ma, GS; Sheng, CS; Wang, JG, 2013
)
0.64
" Safety profile and tolerability assessments included monitoring of adverse events."( Efficacy and safety of two ramipril and hydrochlorothiazide fixed-dose combination formulations in adults with stage 1 or stage 2 arterial hypertension evaluated by using ABPM.
Gomes, MA; Kohlmann, O; Nobre, F; Oigman, W; Pereira-Barretto, AC; Póvoa, R; Rocha, JC, 2013
)
0.66
" The incidence of adverse events was 23."( Efficacy and safety of two ramipril and hydrochlorothiazide fixed-dose combination formulations in adults with stage 1 or stage 2 arterial hypertension evaluated by using ABPM.
Gomes, MA; Kohlmann, O; Nobre, F; Oigman, W; Pereira-Barretto, AC; Póvoa, R; Rocha, JC, 2013
)
0.66
" Adverse drug reactions were rare (n = 19), and no serious adverse drug reactions occurred."( Safety, tolerability, and efficacy of a fixed-dose combination of olmesartan 40 mg and hydrochlorothiazide 12.5/25 mg in daily practice.
Bramlage, P; Fronk, EM; Ketelhut, R; Schmieder, RE; Wolf, WP; Zemmrich, C, 2013
)
0.61
"Our data confirm randomized trial data concerning safe and efficient blood pressure reduction using a fixed-dose combination of olmesartan 40 mg and HCTZ 12."( Safety, tolerability, and efficacy of a fixed-dose combination of olmesartan 40 mg and hydrochlorothiazide 12.5/25 mg in daily practice.
Bramlage, P; Fronk, EM; Ketelhut, R; Schmieder, RE; Wolf, WP; Zemmrich, C, 2013
)
0.61
"from a total of 112 treatment-naive patients and 381 previously treated patients eligible for safety analysis, there were only 3 patients with adverse events, and 2 of which were considered possibly related to candesartan (0."( Safety and effectiveness of candesartan and candesartan/HCT fixed dose combination in patients with hypertension.
Pohan, T; Setiawati, A, 2013
)
0.39
" Incidence of adverse events (AEs) and serious AEs (SAEs) was recorded as safety variables."( Real-life effectiveness, safety, and tolerability of amlodipine/valsartan or amlodipine/valsartan/hydrochlorothiazide single-pill combination in patients with hypertension from Pakistan.
Abid, R; Afzal, J; Iktidar, S; Khan, W; Kumar, K; Maheshwary, N; Moin, N; Qadir, M; Sakrani, J; Siddiqi, A, 2014
)
0.62
"Hypothyroidism is a common clinical side effect of lithium treatment, whereas parkinsonism is a very rare adverse event."( Parkinsonism and severe hypothyroidism in an elderly patient: a case of lithium toxicity due to pharmacological interactions.
Basile, G; Epifanio, A; Mandraffino, R; Trifirò, G, 2014
)
0.4
" The incidence of adverse events was similar across the treatment groups."( Open-label study assessing the long-term efficacy and safety of triple olmesartan/amlodipine/hydrochlorothiazide combination therapy for hypertension.
Ammentorp, B; de la Sierra, A; Laeis, P; Volpe, M, 2014
)
0.62
" Drug-related adverse events with an incidence ⩾ 2% in the L100/H12."( Efficacy and safety of losartan 100 mg/hydrochlorothiazide 12.5 mg in Japanese subjects with essential hypertension: two randomized, controlled trials.
Azuma, K; Fujimoto, G; Fujita, KP; Hanson, ME; Nishida, C; Numaguchi, H; Rakugi, H; Shimada, K; Shirakawa, M; Tsuchihashi, T; Yamaguchi, H, 2014
)
0.67
" Adverse events were assessed."( Efficacy and safety of fixed-dose losartan/hydrochlorothiazide/amlodipine combination versus losartan/hydrochlorothiazide combination in Japanese patients with essential hypertension.
Azuma, K; Fujita, KP; Nishida, C; Numaguchi, H; Rakugi, H; Shimada, K; Shirakawa, M; Tsuchihashi, T; Yamaguchi, H, 2015
)
0.68
" Safety and tolerability parameters included adverse events."( Long-term safety of nebivolol and valsartan combination therapy in patients with hypertension: an open-label, single-arm, multicenter study.
Finck, A; Giles, TD; Li, H; Neutel, JM; Punzi, H; Weiss, RJ, 2014
)
0.4
" Overall, the olmesartan/amlodipine FDC was well tolerated, and there were no serious adverse events associated with medication."( A multicenter, non-comparative study to evaluate the efficacy and safety of fixed-dose olmesartan/amlodipine in Korean patients with hypertension who are naïve or non-responders to anti-hypertensive monotherapy (ACE-HY study).
Ahn, Y; Bae, JH; Jung, HW; Kang, DH; Kim, CH; Kim, KI; Park, CG, 2015
)
0.42
"CLOROTIC is the first large-scale trial to evaluate whether the addition of a thiazide diuretic (hydrochlorothiazide) to a loop diuretic (furosemide) is a safe and effective strategy for improving congestive symptoms resulting from HF."( Rationale and Design of the "Safety and Efficacy of the Combination of Loop with Thiazide-type Diuretics in Patients with Decompensated Heart Failure (CLOROTIC) Trial:" A Double-Blind, Randomized, Placebo-Controlled Study to Determine the Effect of Combin
Casado, J; Formiga, F; Freitas Ramírez, A; Manzano, L; Morales-Rull, JL; Trullàs, JC, 2016
)
0.65
" Adverse events (AEs) were reported in 75."( Safety and tolerability of azilsartan medoxomil in subjects with essential hypertension: a one-year, phase 3, open-label study.
Barger, B; Handley, A; Lloyd, E; Roberts, A, 2016
)
0.43
" The adverse events (AEs) during both treatment periods were generally mild."( The efficacy and long-term safety of a triple combination of 80 mg telmisartan, 5 mg amlodipine and 12.5 mg hydrochlorothiazide in Japanese patients with essential hypertension: a randomized, double-blind study with open-label extension.
Higaki, J; Ikeda, H; Komuro, I; Kuroki, D; Nishimura, S; Ogihara, T; Shiki, K; Taniguchi, A; Ugai, H, 2017
)
0.67
" The most frequently reported adverse reactions included headache (3."( Safety and efficacy of fimasartan in Mexican patients with grade 1-2 essential hypertension.
Banda-Elizondo, RG; Cardona-Muñoz, EG; Conde-Carmona, I; Esturau-Santalo, RM; García-Castillo, A; González-Gálvez, G; Guerra-López, A; Leiva-Pons, JL; López-Alvarado, A; Pascoe-González, S; Sánchez-Mejorada, G; Velasco-Sánchez, RG; Vidrio-Velázquez, M; Villeda-Espinosa, E,
)
0.13
"Fimasartan is safe and effective in Mexican subjects with grade 1-2 essential hypertension."( Safety and efficacy of fimasartan in Mexican patients with grade 1-2 essential hypertension.
Banda-Elizondo, RG; Cardona-Muñoz, EG; Conde-Carmona, I; Esturau-Santalo, RM; García-Castillo, A; González-Gálvez, G; Guerra-López, A; Leiva-Pons, JL; López-Alvarado, A; Pascoe-González, S; Sánchez-Mejorada, G; Velasco-Sánchez, RG; Vidrio-Velázquez, M; Villeda-Espinosa, E,
)
0.13
" Treatment-emergent adverse events/serious adverse events occurred in 78."( Comparison of long-term safety of fixed-dose combinations azilsartan medoxomil/chlorthalidone vs olmesartan medoxomil/hydrochlorothiazide.
Barger, B; Cushman, WC; Handley, A; Lloyd, E; Neutel, JM, 2017
)
0.66
" High adherence rates and few adverse effects were observed in Very-Elderly patients receiving combination (n = 32) and high-dose (n = 34) therapies and in Young/Elderly patients receiving combination (n = 69) and high-dose (n = 66) therapies."( Losartan/hydrochlorothiazide combination is safe and effective for morning hypertension in Very-Elderly patients.
Anegawa, T; Fukuda, K; Fukumoto, Y; Imaizumi, T; Iwamoto, Y; Kai, H; Kajimoto, H; Uchiwa, H, 2018
)
0.9
"Most adverse events (AEs) were mild or moderate in intensity, and no deaths or treatment-related serious AEs were reported."( A phase III, open-label, multicenter study to evaluate the safety and efficacy of long-term triple combination therapy with azilsartan, amlodipine, and hydrochlorothiazide in patients with essential hypertension.
Nishiyama, Y; Rakugi, H; Sano, Y; Shimizu, K; Umeda, Y, 2018
)
0.68
"A drug must reach the central nervous system (CNS) in order to directly cause CNS adverse effects (AEs)."( Quantification of Hydrochlorothiazide and Ramipril/Ramiprilate in Blood Serum and Cerebrospinal Fluid: A Pharmacokinetic Assessment of Central Nervous System Adverse Effects.
Fuhr, U; Holzgrabe, U; Kinzig, M; Schroeter, M; Sigaroudi, A; Sörgel, F; Stelzer, C; Wahl, O, 2018
)
0.81
" Safety and tolerability were assessed by the incidence rate of adverse events (AEs) and discontinuation."( Real-World Effectiveness and Safety of a Single-Pill Combination of Olmesartan/Amlodipine/Hydrochlorothiazide in Korean Patients with Essential Hypertension (RESOLVE): A Large, Observational, Retrospective, Cohort Study.
Park, SJ; Rhee, SJ, 2020
)
0.78
"The outcomes of interest were adverse kidney events (ie, eGFR decline ≥30%, dialysis, or kidney transplantation), cardiovascular events (composite of myocardial infarction, coronary revascularization, heart failure, or atrial fibrillation), all-cause mortality, and electrolyte anomalies (ie, sodium or potassium levels outside reference ranges)."( Comparison of Clinical Outcomes and Safety Associated With Chlorthalidone vs Hydrochlorothiazide in Older Adults With Varying Levels of Kidney Function.
Bugeja, A; Burns, K; Canney, M; Edwards, C; Hundemer, GL; Knoll, G; Petrcich, W; Sood, MM, 2021
)
0.85
" The therapy was safe and well tolerated."( Real-World Effectiveness and Safety of a Single-Pill Combination of Olmesartan/Amlodipine/Hydrochlorothiazide in Korean Patients with Hypertension and Cardiovascular Risk Factors.
Hong, JH; Hyun, D; Kim, GH; Kim, HL; Kim, W; Lim, S; Min, KW; Oh, J; Park, SD; Shin, J, 2023
)
1.13

Pharmacokinetics

hydrochlorothiazide's mean biological half-life (t1/2) and apparent volume of distribution (Vdarea) in normal subjects were found to vary greatly among 11 studies reported between 1976 and 1986. The synergistic antihypertensive pharmacodynamic interaction b was evaluated in a multicenter, multiple-dose, open-label, 4-cohort, parallel-group study.

ExcerptReferenceRelevance
"In spite of more than three decades of wide use of hydrochlorothiazide as a diuretic, its mean biological half-life (t1/2) and apparent volume of distribution (Vdarea) in normal subjects were found to vary greatly among 11 studies reported between 1976 and 1986."( Large differences in the biological half-life and volume of distribution of hydrochlorothiazide in normal subjects from eleven studies. Correlation with their last blood sampling times.
Chen, TM; Chiou, WL, 1992
)
0.76
"Co-administration of drugs with complementary action is a rational approach to the treatment of hypertension provided that the drugs are free of mutual pharmacokinetic interactions."( The pharmacokinetics of co-administered lisinopril and hydrochlorothiazide.
Swaisland, AJ, 1991
)
0.53
" Similar differences have been reported for such patient groups when the drugs were administered separately, indicating an absence of pharmacokinetic interaction."( The effects of age and renal impairment on the pharmacokinetics of co-administered lisinopril and hydrochlorothiazide.
Connell, PA; Hosie, J; Laher, MS; Mulkerrins, E; Smith, RP; Swaisland, AJ, 1991
)
0.5
" However, when given with HCT, the mean AUC and Cmax of enalaprilat were reduced up to 20 per cent compared with enalapril administered alone."( Pharmacokinetic comparison of a combination tablet of enalapril and hydrochlorothiazide with enalapril and hydrochlorothiazide tablets administered together and separately.
Broadbear, J; Conway, EL; Drummer, OH; Howes, LG; Louis, WJ; Phillips, PA,
)
0.37
" No significant pharmacokinetic interaction was found between cilazapril and hydrochlorothiazide."( Pharmacokinetics and effects on renal function following cilazapril and hydrochlorothiazide alone and in combination in healthy subjects and hypertensive patients.
Grynne, B; Kleinbloesem, CH; Nilsen, OG; Romfo, OS; Sellevold, OF; Smedsrud, A; Williams, PE, 1989
)
0.74
" Mean peak concentration of triamterene was increased in the elderly patients compared with the data of young healthy volunteers."( Pharmacokinetics of triamterene in geriatric patients--influence of piretanide and hydrochlorothiazide.
Jung, R; Mühlberg, W; Mutschler, E; Platt, D; Spahn, H, 1989
)
0.5
" As a result of the pharmacokinetic findings caution may be indicated in the clinical dosage of the diuretics particularly when in fixed dose combination."( The pharmacokinetics of amiloride-hydrochlorothiazide combination in the young and elderly.
Ismail, Z; Parke, W; Smithurst, BA; Triggs, EJ, 1989
)
0.56
" No difference in any of the drug pharmacokinetic parameters could be detected between the hypertensives and the normal elderly subjects."( A comparative study of the pharmacokinetics and pharmacodynamics of atenolol, hydrochlorothiazide and amiloride in normal young and elderly subjects and elderly hypertensive patients.
Adam, HK; Castleden, CM; Fitzsimons, TJ; Ryan, J; Sabanathan, K, 1987
)
0.5
" Triamterin pharmacokinetic studies may be used for the screening of hypertensive patients as potential candidates for triampur treatment."( [Relation between the hypotensive effect of triampur and its pharmacokinetics in patients with hypertension].
Kuznetsov, GP; Lebedev, PA, 1986
)
0.27
"6 h after both treatments and the half-life of disposition was calculated to be 4-5 h, being somewhat longer after the combination tablet."( Pharmacokinetics of mepindolol administered alone and in combination with hydrochlorothiazide--a bioequivalence study.
Krause, W; Lennert, C,
)
0.36
" The main pharmacokinetic parameters of acebutolol did not differ significantly: AUC 4492 +/- 272 micrograms l-1h given alone versus 4118 +/- 354 micrograms l-1h with HCT, half-life (7,69 +/- 0,32 h vs 8,10 +/- 0,72 h) and renal clearance (13,1 +/- 0,5 lh-1 vs 13,8 +/- 0,9 lh-1), respectively."( Pharmacokinetics in man of acebutolol and hydrochlorothiazide as single agents and in combination.
Delhotal, B; Flouvat, B; Gaillot, J; Le Liboux, A; Roux, A, 1983
)
0.53
"The article deals with the shortcomings of pharmacokinetic models in predicting tissue-concentrations of drugs."( [Pharmacokinetic problems in surgery].
Fabian, W; Fellmann, E; Hropot, M; Muschaweck, R; Sörgel, F, 1980
)
0.26
" We assessed pharmacokinetic and pharmacodynamic interactions of the ACE inhibitor cilazapril and the beta-blocker propranolol in healthy volunteers and patients with essential hypertension."( Review of studies on the clinical pharmacodynamics of cilazapril.
Belz, GG; Breithaupt, K; Erb, K, 1994
)
0.29
" The controlled-release formulation gave less variable plasma metoprolol concentrations, Cmax 138 nmol."( The pharmacokinetics and pharmacodynamics of metoprolol after conventional and controlled-release administration in combination with hydrochlorothiazide in healthy volunteers.
Abrahamsson, B; Lundborg, P; Walter, M; Wieselgren, I, 1993
)
0.49
" The implication of the present study in physiological pharmacokinetic and hepatic modeling is discussed."( Intrahepatic distribution of hydrochlorothiazide and quinidine in rats: implications in pharmacokinetics.
AbdelHameed, MH; Chen, TM; Chiou, WL, 1993
)
0.58
" A pharmacokinetic characteristics of new drug adalate SL with two-step liberation of nifedipine."( [The pharmacokinetics of different drug forms of nifedipine when used singly and in a course as monotherapy and in combination with Cordanum and triampur preparations in patients with arterial hypertension].
Ignat'ev, VG; Kukes, VG; Pavlov, SS; Starodubtsev, AK,
)
0.13
"To support the use of a combination of losartan, a highly specific and selective AT1 angiotensin II receptor antagonist, and hydrochlorothiazide for treatment of hypertension, a pharmacokinetic drug interaction study was conducted."( Absence of a pharmacokinetic interaction between losartan and hydrochlorothiazide.
Capra, NL; Goldberg, MR; Hsieh, JY; Lin, CC; Lo, MW; McCrea, JB; Tomasko, L, 1995
)
0.74
"To investigate the potential for pharmacokinetic interactions between moexipril, a new converting enzyme inhibitor, and hydrochlorothiazide after single dose administration."( Lack of a pharmacokinetic interaction between moexipril and hydrochlorothiazide.
Angehrn, JC; Bonn, R; Cawello, W; De Schepper, PJ; Hutt, V; Michaelis, K; Salomon, P; Verbesselt, R, 1996
)
0.74
" The Cmax of moexipril and the metabolite (data of the metabolite in parenthesis) were 245."( Lack of a pharmacokinetic interaction between moexipril and hydrochlorothiazide.
Angehrn, JC; Bonn, R; Cawello, W; De Schepper, PJ; Hutt, V; Michaelis, K; Salomon, P; Verbesselt, R, 1996
)
0.54
"The coadministration of moexipril with hydrochlorothiazide had no demonstrable effect on the measured pharmacokinetic parameters of moexipril, its active metabolite moexiprilat or hydrochlorothiazide."( Lack of a pharmacokinetic interaction between moexipril and hydrochlorothiazide.
Angehrn, JC; Bonn, R; Cawello, W; De Schepper, PJ; Hutt, V; Michaelis, K; Salomon, P; Verbesselt, R, 1996
)
0.81
"The aim of this series of studies was to determine the potential for pharmacokinetic interaction between candesartan (administered orally as the prodrug candesartan cilexetil) and hydrochlorothiazide (HCTZ), nifedipine, glibenclamide, warfarin, digoxin or the components of an oral contraceptive formulation."( Pharmacokinetic drug interaction studies with candesartan cilexetil.
Högemann, A; Jonkman, JH; Lins, R; Sennewald, R; van Heiningen, PN; van Lier, JJ, 1997
)
0.49
" Therefore, the aim of this study was to examine the dose linearity of TA and the pharmacokinetic and pharmacodynamic interaction of triamterene and hydrochlorothiazide."( Pharmacokinetics and pharmacodynamics of triamterene and hydrochlorothiazide and their combination in healthy volunteers.
Knauf, H; Möhrke, W; Mutschler, E, 1997
)
0.74
" Zolmitriptan plasma concentrations were higher in women than in men, with higher values of AUC and Cmax and lower total clearance in women."( Pharmacokinetics and pharmacodynamics of zolmitriptan in patients with mild to moderate hypertension: a double-blind, placebo-controlled study.
Cleary, EW; Dilzer, SC; Huffman, CS; Lasseter, KC; Smith, DA; Watkins, S, 1998
)
0.3
" The purpose of this investigation was to determine whether a drug-drug pharmacokinetic interaction exists between diltiazem and hydrochlorothiazide."( Steady-state pharmacokinetics of diltiazem and hydrochlorothiazide administered alone and in combination.
Dimmitt, DC; Geising, DH; Lanman, RC; Morrill, MB; Weir, SJ, 1998
)
0.76
"To evaluate the pharmacokinetic interaction and bioequivalence of a combination formulation of the angiotensin-converting enzyme inhibitor fosinopril and the diuretic hydrochlorothiazide (HCTZ)."( Fosinopril and hydrochlorothiazide combination versus individual components: lack of a pharmacokinetic interaction.
Brennan, J; Chang, SY; Delaney, CL; Liao, W; Morgenthien, EA; Much, DR; Stouffer, BC; Uderman, HD; VanHarken, D; Weaver, J, 1999
)
0.85
"Fosinopril and HCTZ in a combination tablet display pharmacokinetic profiles similar to those achieved when either drug is administered alone or when coadministered in separate tablets."( Fosinopril and hydrochlorothiazide combination versus individual components: lack of a pharmacokinetic interaction.
Brennan, J; Chang, SY; Delaney, CL; Liao, W; Morgenthien, EA; Much, DR; Stouffer, BC; Uderman, HD; VanHarken, D; Weaver, J, 1999
)
0.66
" Furthermore, the pharmacodynamic action of diuretics was not significantly altered in the elderly."( Renal handling of drugs in the healthy elderly. Creatinine clearance underestimates renal function and pharmacokinetics remain virtually unchanged.
Bischoff, I; Block, S; Fliser, D; Hanses, A; Joest, M; Mutschler, E; Ritz, E, 1999
)
0.3
" Non-compartmental pharmacokinetic parameters of fosinoprilat and HCTZ were determined from blood and urine samples obtained over 48 h starting on Day 1 (single dose) and Day 5 (steady state): maximum serum concentration (Cmax ), time to maximum serum concentration (tmax ), area under the serum concentration-time curve during the dosing interval (AUC), cumulative urinary excretion (CUE) and the accumulation index (AI; ratio of AUC-day 5/AUC-day 1)."( Fosinopril/hydrochlorothiazide: single dose and steady-state pharmacokinetics and pharmacodynamics.
Lins, R; Mangold, B; O'Grady, P; Yee, KF, 1999
)
0.69
"Fosinoprilat pharmacokinetic parameters on day 1 in renally impaired vs normal patients: Cmax=387+/-0."( Fosinopril/hydrochlorothiazide: single dose and steady-state pharmacokinetics and pharmacodynamics.
Lins, R; Mangold, B; O'Grady, P; Yee, KF, 1999
)
0.69
"In renally impaired subjects fosinopril and HCTZ can be coadministered without undue increases in fosinoprilat concentrations or any clinically significant pharmacodynamic effects."( Fosinopril/hydrochlorothiazide: single dose and steady-state pharmacokinetics and pharmacodynamics.
Lins, R; Mangold, B; O'Grady, P; Yee, KF, 1999
)
0.69
"The pharmacokinetic and dynamic interactions of the angiotensin-converting enzyme (ACE) inhibitor imidapril with other therapeutic principles used in hypertension and heart failure were evaluated."( Pharmacokinetic and dynamic interactions of the angiotensin-converting enzyme inhibitor imidapril with hydrochlorothiazide, bisoprolol and nilvadipine.
Belz, GG; Breithaupt-Grögler, K; Meurer-Witt, B; Ungethüm, W, 2001
)
0.53
" Plasma concentrations of imidaprilat and H were followed up to 48 h, those of B and N up to 24 h and area under the concentration time curve (AUC), maximum plasma concentration (Cmax) and time to Cmax (tmax) were determined."( Pharmacokinetic and dynamic interactions of the angiotensin-converting enzyme inhibitor imidapril with hydrochlorothiazide, bisoprolol and nilvadipine.
Belz, GG; Breithaupt-Grögler, K; Meurer-Witt, B; Ungethüm, W, 2001
)
0.53
"The combination of imidapril with a diuretic, beta-adrenoceptor antagonist or calcium-channel blocker seems a reasonable and safe treatment option when striving for additive pharmacodynamic effects not accompanied by relevant pharmacokinetic interactions."( Pharmacokinetic and dynamic interactions of the angiotensin-converting enzyme inhibitor imidapril with hydrochlorothiazide, bisoprolol and nilvadipine.
Belz, GG; Breithaupt-Grögler, K; Meurer-Witt, B; Ungethüm, W, 2001
)
0.53
" Pharmacokinetic-pharmacodynamic (PK/PD) modeling was applied to investigate the pharmacokinetic and pharmacodynamic interaction between irbesartan and HCTZ in renal hypertensive dogs at non-steady-state and steady-state."( Pharmacokinetic and pharmacodynamic interaction between irbesartan and hydrochlorothiazide in renal hypertensive dogs.
Huang, XH; Li, J; Qiu, FR; Xie, HT, 2005
)
0.56
" Four open-label studies investigated the pharmacokinetic interactions between aliskiren 300 mg and the antihypertensive drugs amlodipine 10 mg (n = 18), valsartan 320 mg (n = 18), hydrochlorothiazide 25 mg (HCTZ, n = 22) and ramipril 10 mg (n = 17) in healthy subjects."( Lack of pharmacokinetic interactions of aliskiren, a novel direct renin inhibitor for the treatment of hypertension, with the antihypertensives amlodipine, valsartan, hydrochlorothiazide (HCTZ) and ramipril in healthy volunteers.
Bizot, MN; Denouel, J; Dieterich, HA; Dole, WP; Kemp, C; Vaidyanathan, S; Valencia, J; Yeh, CM; Zhao, C, 2006
)
0.72
" This trial investigated the possibility of pharmacokinetic interactions between the AT1 receptor antagonist olmesartan medoxomil and the thiazide diuretic hydrochlorothiazide in healthy subjects."( Pharmacokinetics of olmesartan medoxomil plus hydrochlorothiazide combination in healthy subjects.
Bolbrinker, J; Huber, M; Kreutz, R, 2006
)
0.79
" The primary pharmacokinetic parameters evaluated were: the area under the plasma concentration versus time curve at steady state (AUCss,tau), the maximum plasma concentration at steady state (Css,max), and the time at which Css,max occurred (tmax)."( Pharmacokinetics of olmesartan medoxomil plus hydrochlorothiazide combination in healthy subjects.
Bolbrinker, J; Huber, M; Kreutz, R, 2006
)
0.59
"Complete data sets from 17 subjects were available for pharmacokinetic analyses."( Pharmacokinetics of olmesartan medoxomil plus hydrochlorothiazide combination in healthy subjects.
Bolbrinker, J; Huber, M; Kreutz, R, 2006
)
0.59
"These results show that there is little or no potential for a clinically relevant pharmacokinetic interaction between olmesartan medoxomil 20 mg and hydrochlorothiazide 25 mg, and therefore dosage adjustment should not be necessary when they are co-administered."( Pharmacokinetics of olmesartan medoxomil plus hydrochlorothiazide combination in healthy subjects.
Bolbrinker, J; Huber, M; Kreutz, R, 2006
)
0.79
"The pharmacokinetic and pharmacodynamic interactions between tolvaptan and furosemide or hydrochlorothiazide (HCTZ) were determined in a single-center, randomized, open-label, parallel-arm, 3-period crossover study conducted in healthy white (Caucasian) men."( Pharmacokinetic and pharmacodynamic interaction between tolvaptan, a non-peptide AVP antagonist, and furosemide or hydrochlorothiazide.
Bramer, SL; Bricmont, P; Shoaf, SE; Zimmer, CA, 2007
)
0.77
" Based on the 90% confidence interval of the individual ratios for Cmax and AUC0-inf, it was concluded that the test formulation is bioequivalent to the reference Hyzaar formulation with respect to the rate and extent of absorption of both LOS and HCTZ."( Simultaneous determination of losartan and hydrochlorothiazide in human plasma by LC/MS/MS with electrospray ionization and its application to pharmacokinetics.
Andraus, MH; Azevedo, CP; Borges, BC; Borges, NC; Moreira, RF; Moreno, RA; Salvadori, MC, 2009
)
0.62
" The mean plasma concentration-time profiles of puerarin and hydrochlorothiazide at different dosages of medication administration were processed by 3P97 pharmacokinetic software and SPSS statistics 17."( [Pharmacokinetics of puerarin and hydrochlorothiazide from maijunan tablets in rats].
Chen, Y; Du, P; Han, FM; Zhang, X, 2009
)
0.87
"The steady-state pharmacokinetic (PK) interaction potential between amlodipine (10 mg), valsartan (320 mg), and hydrochlorothiazide (HCTZ; 25 mg) was evaluated in patients with hypertension in a multicenter, multiple-dose, open-label, 4-cohort, parallel-group study."( Evaluation of pharmacokinetic interactions between amlodipine, valsartan, and hydrochlorothiazide in patients with hypertension.
Ayalasomayajula, S; Bhad, P; Jarugula, V; Karan, R; Leon, S; Riviere, GJ; Sunkara, G, 2011
)
0.81
"There was no pharmacokinetic interaction between candesartan 32 mg and HCT 25 mg during concomitant administration."( Pharmacokinetic interaction study with fixed high dose combinations of candesartan cilexetil and hydrochlorothiazide.
Aberg, JG; Karlson, BW; Olofsson, B, 2011
)
0.59
"There was no pharmacokinetic interaction found between the high doses of candesartan 32 mg and HCT 25 mg."( Pharmacokinetic interaction study with fixed high dose combinations of candesartan cilexetil and hydrochlorothiazide.
Aberg, JG; Karlson, BW; Olofsson, B, 2011
)
0.59
"To compare the pharmacokinetic (PK) profiles and evaluate the PK interaction of hydrochlorothiazide (HCTZ) used alone and in combination with benazepril (BENA) or valsartan (VAL) in healthy Chinese volunteers."( Pharmacokinetic profiles of hydrochlorothiazide alone and in combination with benazepril or valsartan in healthy Chinese volunteers: evaluation of the potential interaction.
Huang, Y; Jiang, J; Li, Y; Liu, H; Tian, L; Xie, S; Xu, L, 2011
)
0.89
" The apparent terminal half-life (t(1/2)) and the time to C(max) (tmax) were unchanged between the two studies."( Pharmacokinetic profiles of hydrochlorothiazide alone and in combination with benazepril or valsartan in healthy Chinese volunteers: evaluation of the potential interaction.
Huang, Y; Jiang, J; Li, Y; Liu, H; Tian, L; Xie, S; Xu, L, 2011
)
0.66
" The method uses 100 µl plasma and covers the calibration range 1-160 ng/ml for CAN and 2-160 ng/ml for HCTZ for routine pharmacokinetic studies in humans."( LC-MS/MS method for simultaneous estimation of candesartan and hydrochlorothiazide in human plasma and its use in clinical pharmacokinetics.
Bharathi, DV; Chatki, PK; Hotha, KK; Satyanarayana, V; Venkateswarlu, V, 2012
)
0.62
" The developed assay was applied to an oral pharmacokinetic study in humans."( LC-MS/MS method for simultaneous estimation of candesartan and hydrochlorothiazide in human plasma and its use in clinical pharmacokinetics.
Bharathi, DV; Chatki, PK; Hotha, KK; Satyanarayana, V; Venkateswarlu, V, 2012
)
0.62
" Saliva and plasma samples were collected for 3-5 half-life values of sitagliptin, cinacalcet, metformin, montelukast, tolterodine, hydrochlorothiazide (HCT), lornoxicam, azithromycin, diacerhein, rosuvastatin, cloxacillin, losartan and tamsulosin after oral dosing."( Saliva versus plasma pharmacokinetics: theory and application of a salivary excretion classification system.
Arafat, T; Idkaidek, N, 2012
)
0.58
"The 90% confidence intervals for the test/reference ratio of the pharmacokinetic parameters in fasting state (mean Cmax, AUC0-t, and AUC0-∞) were within the acceptable range of 80."( A comparative pharmacokinetic study of a fixed dose combination for essential hypertensive patients: a randomized crossover study in healthy human volunteers.
Biswas, E; Choudhury, H; Ghosh, B; Gorain, B; Halder, D; Pal, TK; Sarkar, AK; Sarkar, P, 2013
)
0.39
" The pharmacokinetic properties of each drug after co-administration of VAL and HCT were compared with those of each drug administered alone."( Pharmacokinetic interactions of valsartan and hydrochlorothiazide: an open-label, randomized, 4-period crossover study in healthy Egyptian male volunteers.
Hedaya, MA; Helmy, SA, 2013
)
0.65
" The interaction of HCT with other angiotensin-receptor blockers should be investigated to determine whether this interaction is limited to VAL or if other angiotensin-receptor blockers have the same pharmacokinetic interactions."( Pharmacokinetic interactions of valsartan and hydrochlorothiazide: an open-label, randomized, 4-period crossover study in healthy Egyptian male volunteers.
Hedaya, MA; Helmy, SA, 2013
)
0.65
" The pharmacokinetic parameters were calculated, and the 90% confidence intervals (CIs) of the geometric mean ratio (test/reference) of the parameters were obtained by analysis of variance (ANOVA) on logarithmically transformed data."( Pharmacokinetic properties and bioequivalence of olmesartan medoxomil/hydrochlorothiazide in healthy Korean male subjects.
Chae, SW; Choi, Y; Im, YJ; Jeon, JY; Jin, C; Jung, JA; Kim, MG; Kim, Y; Park, K, 2014
)
0.64
" The pharmacokinetic parameters AUC0-t, AUC0-∞, Cmax, tmax, and other pharmacokinetics parameters were determined from plasma concentration-time profiles for both test and reference formulations of losartan/hydrochlorothiazide 50 + 12."( Pharmacokinetic comparison and bioequivalence evaluation of losartan/ hydrochlorothiazide tablet between Asian Indian and Japanese volunteers.
Jain, R; Khuroo, A; Kumar, S; Kurachi, K; Monif, T; Reyar, S; Singla, AK, 2014
)
0.82
" The ratios of least square means for AUC0-t and Cmax and the affiliated 90% confidence intervals were within acceptance range recommended by PMDA."( Pharmacokinetic comparison and bioequivalence evaluation of losartan/ hydrochlorothiazide tablet between Asian Indian and Japanese volunteers.
Jain, R; Khuroo, A; Kumar, S; Kurachi, K; Monif, T; Reyar, S; Singla, AK, 2014
)
0.64
" Although Asian Indian and Japanese volunteers are ethnically different, results of these studies indicate that pharmacokinetic parameters of Asian Indian and Japanese volunteers are comparable to each other in terms of bioavailability of losartan, losartan carboxylic acid and hydrochlorothiazide."( Pharmacokinetic comparison and bioequivalence evaluation of losartan/ hydrochlorothiazide tablet between Asian Indian and Japanese volunteers.
Jain, R; Khuroo, A; Kumar, S; Kurachi, K; Monif, T; Reyar, S; Singla, AK, 2014
)
0.81
" The current pharmacokinetic-pharmacodynamic model was based on the non-competitive pharmacodynamic interaction of two drugs acting on different physiological processes."( Pharmacokinetic-pharmacodynamic model of the antihypertensive interaction between telmisartan and hydrochlorothiazide in spontaneously hypertensive rats.
Chen, Y; Hao, K; Liu, X; Zhao, X, 2014
)
0.62
" The noncompetitive pharmacodynamic interaction assumed that the decreased blood pressure was attributed to the inhibitory function of telmisartan and stimulatory function of hydrochlorothiazide after administration of these two drugs."( Pharmacokinetic-pharmacodynamic model of the antihypertensive interaction between telmisartan and hydrochlorothiazide in spontaneously hypertensive rats.
Chen, Y; Hao, K; Liu, X; Zhao, X, 2014
)
0.81
"This study evaluated the effects of HCTZ on the pharmacokinetic and pharmacodynamic properties and tolerability of canagliflozin in healthy participants."( Effects of hydrochlorothiazide on the pharmacokinetics, pharmacodynamics, and tolerability of canagliflozin, a sodium glucose co-transporter 2 inhibitor, in healthy participants.
Devineni, D; Polidori, D; Rusch, S; Vaccaro, N; Wajs, E, 2014
)
0.79
" Blood samples were taken before and several times after administration on day 7 of period 1 and on days 28 and 35 of period 2 for canagliflozin and HCTZ pharmacokinetic analyses using LC-MS/MS."( Effects of hydrochlorothiazide on the pharmacokinetics, pharmacodynamics, and tolerability of canagliflozin, a sodium glucose co-transporter 2 inhibitor, in healthy participants.
Devineni, D; Polidori, D; Rusch, S; Vaccaro, N; Wajs, E, 2014
)
0.79
"Adding canagliflozin treatment to healthy participants on HCTZ treatment had no notable pharmacokinetic or pharmacodynamic effects; canagliflozin coadministered with HCTZ was generally well tolerated, with no unexpected tolerability concerns."( Effects of hydrochlorothiazide on the pharmacokinetics, pharmacodynamics, and tolerability of canagliflozin, a sodium glucose co-transporter 2 inhibitor, in healthy participants.
Devineni, D; Polidori, D; Rusch, S; Vaccaro, N; Wajs, E, 2014
)
0.79
"The objective of the present study was to develop population pharmacokinetic models for olmesartan medoxomil and hydrochlorothiazide and to investigate the influence of demographic factors on these population pharmacokinetics."( Development of a population pharmacokinetic model to describe olmesartan medoxomil/ hydrochlorothiazide (20/12.5 mg) FDC tablet in male healthy South Korean subjects.
Back, HM; Baek, IH; Chae, JW; Jung, SH; Kang, W; Kwon, KI; Lee, BY; Seo, JW; Song, BJ; Yun, HY, 2014
)
0.84
" All evaluations indicated that the pharmacokinetic profiles of olmesartan medoxomil and hydrochlorothiazide were adequately described using our PPK model."( Development of a population pharmacokinetic model to describe olmesartan medoxomil/ hydrochlorothiazide (20/12.5 mg) FDC tablet in male healthy South Korean subjects.
Back, HM; Baek, IH; Chae, JW; Jung, SH; Kang, W; Kwon, KI; Lee, BY; Seo, JW; Song, BJ; Yun, HY, 2014
)
0.85
" The research comprised various studies which includes solubility studies in various vehicles, pseudoternary phase diagram construction, and preparation and characterization of SNEDDS along with in vitro dissolution and in vivo pharmacodynamic profiling."( Development, characterization, and pharmacodynamic evaluation of hydrochlorothiazide loaded self-nanoemulsifying drug delivery systems.
Amin, S; Verma, A; Yadav, E; Yadav, PS, 2014
)
0.64
" This study investigated potential pharmacokinetic drug-drug interactions between empagliflozin and hydrochlorothiazide (HCTZ) or torasemide (TOR)."( Assessing pharmacokinetic interactions between the sodium glucose cotransporter 2 inhibitor empagliflozin and hydrochlorothiazide or torasemide in patients with type 2 diabetes mellitus: a randomized, open-label, crossover study.
Broedl, UC; Heise, T; Macha, S; Mattheus, M; Woerle, HJ, 2015
)
0.85
" Pharmacokinetic parameters of empagliflozin, HCTZ, and TOR were assessed and standard bioequivalence criteria (80%-125%) were applied."( Assessing pharmacokinetic interactions between the sodium glucose cotransporter 2 inhibitor empagliflozin and hydrochlorothiazide or torasemide in patients with type 2 diabetes mellitus: a randomized, open-label, crossover study.
Broedl, UC; Heise, T; Macha, S; Mattheus, M; Woerle, HJ, 2015
)
0.63
" Geometric mean ratios (90% CIs) for empagliflozin AUC over a uniform dosing interval and Cmax at steady state were 107."( Assessing pharmacokinetic interactions between the sodium glucose cotransporter 2 inhibitor empagliflozin and hydrochlorothiazide or torasemide in patients with type 2 diabetes mellitus: a randomized, open-label, crossover study.
Broedl, UC; Heise, T; Macha, S; Mattheus, M; Woerle, HJ, 2015
)
0.63
"No pharmacokinetic drug-drug interaction was observed between empagliflozin and HCTZ or TOR."( Assessing pharmacokinetic interactions between the sodium glucose cotransporter 2 inhibitor empagliflozin and hydrochlorothiazide or torasemide in patients with type 2 diabetes mellitus: a randomized, open-label, crossover study.
Broedl, UC; Heise, T; Macha, S; Mattheus, M; Woerle, HJ, 2015
)
0.63
"The aim of the present study was to compare the pharmacokinetic profiles between a new generic and a branded reference formulation of irbesartan/ hydrochlorothiazide FDC tablets, and to assess the bioequivalence of the two products in healthy Chinese male volunteers."( Pharmacokinetic properties and bioequivalence of two irbesartan/ hydrochlorothiazide fixed-dose combination tablets in healthy male Chinese volunteers.
Hu, X; Liu, J; ShenTu, J; Wu, G; Wu, L; Zhai, Y; Zheng, Y; Zhou, H; Zhu, M, 2015
)
0.85
"For irbesartan, the 90% confidence intervals (CIs) of AUC0-t, AUC0-∞, and Cmax were 103."( Pharmacokinetic properties and bioequivalence of two irbesartan/ hydrochlorothiazide fixed-dose combination tablets in healthy male Chinese volunteers.
Hu, X; Liu, J; ShenTu, J; Wu, G; Wu, L; Zhai, Y; Zheng, Y; Zhou, H; Zhu, M, 2015
)
0.65
" The excellent selectivity for ROMK inhibition over related ion channels and pharmacokinetic properties across preclinical species support further preclinical evaluation of 28 as a new mechanism diuretic."( Discovery of a Potent and Selective ROMK Inhibitor with Pharmacokinetic Properties Suitable for Preclinical Evaluation.
Alonso-Galicia, M; Bailey, T; Bentley, R; Brochu, RM; Chen, J; Corona, A; Felix, JP; Forrest, M; Frie, J; Garcia, ML; Ha, S; Hampton, C; Hernandez, M; Kaczorowski, GJ; Liu, J; Margulis, M; Metzger, J; Owens, K; Pai, LY; Parmee, E; Pasternak, A; Priest, BT; Roy, S; Shah, K; Shahripour, A; Sullivan, K; Swensen, AM; Tang, H; Teumelsan, N; Thomas-Fowlkes, B; Tong, V; Visconti, R; Walsh, SP; Weinglass, A; Yang, L; Zhou, X; Zhu, Y, 2015
)
0.42
" The synergistic antihypertensive pharmacodynamic interaction between telmisartan and hydrochlorothiazide was observed, which was simulated by the inhibitory function of telmisartan and stimulatory function of hydrochlorothiazide after co-administration of the two drugs."( The pharmacokinetic-pharmacodynamic model of telmisartan and hydrochlorothiazide on blood pressure and plasma potassium after long-term administration in spontaneously hypertensive rats.
Chen, Y; Hao, K; Yu, D, 2015
)
0.88
" The mini-tablet combination released the two drugs over 24h in vivo with a steady plasma concentration, a markedly lower Cmax, extended Tmax and better bioavailability."( Mini-tablet combination for sustained release of clonidine hydrochloride and hydrochlorothiazide: Preparation and pharmacokinetics in beagle dogs.
Wang, Y; Xu, B; Zhu, H, 2016
)
0.66
" The pharmacokinetic parameters for topiramate, diltiazem (and active metabolites, desacetyldiltiazem [DEA], N-demethyl diltiazem [DEM]), hydrochlorothiazide, and propranolol (and its active metabolite) were assessed at steady state."( Pharmacokinetic interactions between topiramate and diltiazem, hydrochlorothiazide, or propranolol.
Curtin, CR; Ford, L; Heald, D; Manitpisitkul, P; Shalayda, K; Wang, SS, 2014
)
0.84
" In 3 separate studies, pharmacokinetic drug-drug interactions (DDIs) potential was assessed when LCZ696 was coadministered with hydrochlorothiazide (HCTZ), amlodipine, or carvedilol."( Pharmacokinetic drug-drug interaction assessment between LCZ696, an angiotensin receptor neprilysin inhibitor, and hydrochlorothiazide, amlodipine, or carvedilol.
Greeley, M; Hsiao, HL; Langenickel, TH; Pal, P; Rajman, I; Rebello, S; Roberts, J; Sunkara, G; Zhou, W, 2015
)
0.83
" Compared to the pure crystalline form, amorphous form and physical mixture, HCT in the co-amorphous form exhibited the significantly increased intrinsic dissolution rate, as well as the enhanced bioavailability in the pharmacokinetic study."( Facile formation of co-amorphous atenolol and hydrochlorothiazide mixtures via cryogenic-milling: Enhanced physical stability, dissolution and pharmacokinetic profile.
Cai, B; Cai, T; Gao, Q; Huang, Y; Moinuddin, SM; Ruan, S; Shi, Q, 2017
)
0.71
" Our current study addressed the pharmacokinetic (PK) background of the assumption that CNS concentrations of hydrochlorothiazide (HCT) and ramiprilate may directly cause CNS AEs such as headache and drowsiness."( Quantification of Hydrochlorothiazide and Ramipril/Ramiprilate in Blood Serum and Cerebrospinal Fluid: A Pharmacokinetic Assessment of Central Nervous System Adverse Effects.
Fuhr, U; Holzgrabe, U; Kinzig, M; Schroeter, M; Sigaroudi, A; Sörgel, F; Stelzer, C; Wahl, O, 2018
)
1.03
"To build a physiologically based pharmacokinetic (PBPK) model for fimasartan, amlodipine, and hydrochlorothiazide, and to investigate the drug-drug interaction (DDI) potentials."( Physiologically Based Pharmacokinetic Modeling of Fimasartan, Amlodipine, and Hydrochlorothiazide for the Investigation of Drug-Drug Interaction Potentials.
Jeon, I; Kim, E; Lee, HA; Lee, S; Rhee, SJ; Song, IS; Yu, KS, 2018
)
0.93
"The predicted-to-observed ratios of all the pharmacokinetic parameters met the acceptance criterion."( Physiologically Based Pharmacokinetic Modeling of Fimasartan, Amlodipine, and Hydrochlorothiazide for the Investigation of Drug-Drug Interaction Potentials.
Jeon, I; Kim, E; Lee, HA; Lee, S; Rhee, SJ; Song, IS; Yu, KS, 2018
)
0.71
" The objective of this study was to evaluate the pharmacokinetic interaction among telmisartan, amlodipine, and hydrochlorothiazide."( Pharmacokinetic Interaction Among Telmisartan, Amlodipine, and Hydrochlorothiazide After a Single Oral Administration in Healthy Male Subjects.
Jeon, JY; Kim, MG; Moon, SJ; Yu, KS, 2019
)
0.96
"The pharmacokinetic parameters of telmisartan, amlodipine, and hydrochlorothiazide when administered separately or co-administered were compared, and all the parameters met the criteria for pharmacokinetic equivalence."( Pharmacokinetic Interaction Among Telmisartan, Amlodipine, and Hydrochlorothiazide After a Single Oral Administration in Healthy Male Subjects.
Jeon, JY; Kim, MG; Moon, SJ; Yu, KS, 2019
)
0.99
" Repeat dose pharmacokinetic and pharmacodynamic study of the nano-fixed dose combination (FDC) was done in dexamethasone-induced animal model."( Pharmacokinetic and pharmacodynamic evaluation of nano-fixed dose combination for hypertension.
Bhandari, RK; Bhatia, A; Kaur, N; Malhotra, S; Pandey, AK; Rather, IIG; Shafiq, N; Sharma, S, 2020
)
0.56
" In pharmacokinetic analysis a sustained-release for 7 days was observed in nano-FDC group."( Pharmacokinetic and pharmacodynamic evaluation of nano-fixed dose combination for hypertension.
Bhandari, RK; Bhatia, A; Kaur, N; Malhotra, S; Pandey, AK; Rather, IIG; Shafiq, N; Sharma, S, 2020
)
0.56
" The pharmacokinetic (PK) properties of HCTZ in children are not well characterized, particularly among children with obesity who frequently suffer from hypertension and may, therefore, benefit from HCTZ therapy."( Pharmacokinetics of Hydrochlorothiazide in Children: A Potential Surrogate for Renal Secretion Maturation.
Al-Uzri, A; Boakye-Agyeman, F; Cohen-Wolkowiez, M; Commander, SJ; Harper, B; Hornik, CD; Hornik, CP; Melloni, C; Mendley, SR; Wu, H; Zimmerman, K, 2021
)
0.94
" For comparison, a previously published population pharmacokinetic model for HCTZ was applied to the same data."( Validation of population pharmacokinetic models: a comparison of internal and external validation approaches for hydrochlorothiazide.
Karali, G; Karalis, V; Kousovista, R; Vlasopoulou, K, 2021
)
0.83
"To evaluate if the combination of the product components in the new FDC capsule formulation affects their respective pharmacokinetic and in vitro dissolution patterns."( Pharmacokinetics of a new fixed-dose combination of candesartan cilexetil, hydrochlorothiazide, and rosuvastatin in healthy adult subjects.
Diaz, L; Feleder, EC; Haddad, T; Halabe, EK; Iglesias, M; Mondelo, N; Roldán, E; Sakson, M; Yerino, GA, 2022
)
0.95

Compound-Compound Interactions

The study is to investigate drug-drug interaction (DDI) between olmesartan medoxomil and hydrochlorothiazide (HCTZ) The aim was to compare the time-effect profiles of a once-daily administration of valsartan and amlodipine.

ExcerptReferenceRelevance
"The effect of long-term treatment of hypertension with propranolol, alone or in combination with hydrochlorothiazide and/or dihydralazine, was investigated in 93 patients with various types of hypertension."( [Long-term treatment of arterial hypertension with propranolol. Combination with diuretics and dihydrazinophthalazine].
Ambrosio, G; Corgnati, A; Dal Palù, C; Palatini, P; Pessina, AC, 1978
)
0.48
" The effects of timolol alone and in combination with a fixed dose of hydrochlorothiazide and amiloride have been studied in a double-blind, controlled study in fifty-four patients with mild to moderate essential hypertension."( Evaluation of the effect of timolol alone and in combination with hydrochlorothiazide and amiloride in the treatment of mild to moderate arterial hypertension: a double-blind, controlled study.
Agabiti-Rosei, E; Alicandri, C; Ambrosioni, E; Magnani, B; Miele, N; Muiesan, G, 1976
)
0.73
" L/HCTZ appears to be a well-tolerated combination with efficacy on once-daily dosing superior to that of C/HCTZ."( Treating mild-to-moderate hypertension: a comparison of lisinopril-hydrochlorothiazide fixed combination with captopril and hydrochlorothiazide free combination.
Graham, RD, 1991
)
0.52
" It can be concluded that ramipril alone and in combination with HCTZ is an effective and safe drug for the long-term treatment of essential hypertension."( Efficacy and safety of ramipril in combination with hydrochlorothiazide: results of a long-term study.
Bauer, B; Breitstadt, A; Cairns, V; Froer, KL; Heidbreder, D, 1991
)
0.53
" The results of comparative trials of benazepril with propranolol and nifedipine suggest that benazepril, administered alone or with the diuretic hydrochlorothiazide, is as effective as the other antihypertensive agents alone or in combination with hydrochlorothiazide."( Comparison of benazepril and other antihypertensive agents alone and in combination with the diuretic hydrochlorothiazide.
DeQuattro, V, 1991
)
0.7
" The patients who received carvedilol in combination with HCTZ and were evaluated for efficacy (n = 38) showed a decrease in SBP/DBP from 156/97 at the end of monotherapy to 145/88 mmHg after 10 weeks; the combination of atenolol with HCTZ (n = 44) reduced BP from 162/97 to 147/88."( Safety and antihypertensive efficacy of carvedilol and atenolol alone and in combination with hydrochlorothiazide.
Hörrmann, M; Machwirth, M; van der Does, R; Widmann, L, 1990
)
0.5
"A comparative study was undertaken to examine antihypertensive effects and impact of hydrochlorothiazide (HCT) alone or in combination with triamterene or amiloride on the hemodynamics of 79 patients with Stage II hypertension."( [Comparative study of the hypotensive action of monotherapy using hydrochlorothiazide and its combination with triamterene and amiloride and their effect on hemodynamics at rest and during exercise therapy].
Glezer, GA; Levinzon, AM; Lipko, DS, 1990
)
0.74
"The efficacy of the calcium channel blocker nitrendipine alone and in combination with the beta blocking agent acebutolol or hydrochlorothiazide was tested in 34 patients with moderate essential hypertension."( [Therapy of moderate hypertension with the calcium antagonist nitrendipine in combination with beta receptor blocker or diuretic].
Kolloch, R; Müller, HM; Overlack, A; Stumpe, KO, 1990
)
0.49
"The antihypertensive and metabolic effects of amlodipine, a new calcium-channel blocker, in combination with hydrochlorothiazide (HCTZ) were compared with those of HCTZ in combination with placebo."( Antihypertensive effectiveness of amlodipine in combination with hydrochlorothiazide.
Chrysant, C; Chrysant, SG; Hitchcock, A; Trus, J, 1989
)
0.73
" Enalapril, either alone or in combination with hydrochlorothiazide, effectively controlled blood pressure."( Effects of enalapril alone, and in combination with hydrochlorothiazide, on renin-angiotensin-aldosterone, renal function, salt and water excretion, and body fluid composition.
Bauer, JH; Gaddy, P, 1985
)
0.78
" It is concluded that in a clinical daily practice of a hypertension clinic low doses of spironolactone or of thiazides combined with potassium-sparing agents reduced BP without alteration in lipid or carbohydrate metabolism on long-term follow-up."( Long-term metabolic effects of spironolactone and thiazides combined with potassium-sparing agents for treatment of essential hypertension.
Charru, A; Chatellier, G; Corvol, P; Degoulet, P; Jeunemaitre, X; Julien, J; Ménard, J; Plouin, PF, 1988
)
0.27
"The antihypertensive and biochemical effects of 25 mg hydrochlorothiazide alone or 50 mg hydrochlorothiazide alone or in combination with triamterene (either 37."( Antihypertensive and biochemical effects of different doses of hydrochlorothiazide alone or in combination with triamterene.
Eisalo, A; Gordin, A; Kohvakka, A; Salo, H, 1986
)
0.76
" At the end of 7 weeks of titration and treatment with NTP or PLA combined with HCTZ, SBP had fallen to 133."( Comparison of nitrendipine combined with low-dose hydrochlorothiazide to hydrochlorothiazide alone in mild to moderate essential hypertension.
Glasser, SP; Leibowitz, DA; McMahon, SG; Ram, CV; Schoenberger, JA; Vanov, SK, 1984
)
0.52
"5 mg indapamide per day, alone or in combination with other drugs."( The treatment of hypertension with indapamide alone or in combination with other drugs.
L'Homme, C; Lemieux, G, 1983
)
0.27
" It is concluded that medroxalol combined with hydrochlorothiazide constituted a potent and safe antihypertensive therapy for the duration of the present study."( Medroxalol combined with hydrochlorothiazide in the treatment of hypertension.
Alexander, N; Maronde, RF; Valasquez, M; Vlachakis, ND, 1983
)
0.83
"The preventive affects on recurrent renal calcium stones of water diuresis alone or combined with drugs aimed at lowering urinary calcium were evaluated prospectively in 51 patients with calcium nephrolithiasis."( [Incidence of lithiasic recurrence after a diuretic therapy, alone or combined with treatment by a thiazide diuretic or phosphorus].
Clavel, J; Lacour, B; Sayegh, F; Ulmann, A, 1984
)
0.27
"5 mg, 25 mg, and 50 mg hydrochlorothiazide combined with 400 mg acebutolol was assessed."( Lack of effect of beta-blocker on flat dose response to thiazide in hypertension: efficacy of low dose thiazide combined with beta-blocker.
Banks, RA; Bayliss, J; MacGregor, GA; Markandu, ND; Roulston, J, 1983
)
0.58
" In these patients, the doubling of diuretic dose (hydrochlorothiazide 50 mg + amiloride 5 mg) in combination with atenolol resulted in a further drop in systolic pressure (to 142."( Effects of hydrochlorothiazide combined with amiloride in atenolol-resistant hypertensive patients.
Bentivoglio, M; Corea, L; Verdecchia, P, 1983
)
0.91
"This study was performed to compare the effect of one month's treatment with hydrochlorothiazide (25 mg) in combination with either amiloride (2."( A study of plasma sodium levels in elderly people taking amiloride or triamterene in combination with hydrochlorothiazide.
Bielawska, CA; Fidler, HM; Goldman, J; Hoffbrand, BI; Rai, GS, 1993
)
0.73
" Forty patients with moderate to severe hypertension and daytime ambulatory diastolic blood pressure > or = 90 mm Hg were randomized double-blind to once-daily treatment with either quinapril up to 20 mg (n = 20) or atenolol up to 100 mg (n = 20) as single drugs or in combination with hydrochlorothiazide 25 mg over a period of 12 weeks."( Comparison of quinapril and atenolol as single drugs or in combination with hydrochlorothiazide in moderate to severe hypertensives, using automated ambulatory monitoring.
Lacourcière, Y; Lefebvre, J; Poirier, L; Provencher, P, 1993
)
0.69
"The purpose of this study was to evaluate the long-term safety and efficacy of moexipril, a non-sulphydryl angiotensin converting enzyme inhibitor, alone or in combination with hydrochlorothiazide in older patients with hypertension."( Long-term safety and efficacy of moexipril alone and in combination with hydrochlorothiazide in elderly patients with hypertension.
Stimpel, M; White, WB, 1995
)
0.72
"The antihypertensive effects and the tolerability of losartan and enalapril given alone or in combination with hydrochlorothiazide (HCTZ) were compared in a multicenter, double-blind, randomized, parallel-group, 16-week clinical trial."( Efficacy and tolerability of losartan versus enalapril alone or in combination with hydrochlorothiazide in patients with essential hypertension.
Edelman, JM; Haggert, B; Liss, C; Townsend, R,
)
0.57
" Twenty-eight patients with mild to moderate hypertension were studied (clinic blood pressure > or = 160/95 mmHg), treated with benazepril alone (n = 7) or combined with hydrochlorothiazide (n = 21)."( [Comparison of clinical and ambulatory measurements of blood pressure with benazepril alone or combined with hydrochlorothiazide in hypertension].
Cocco-Guyomarch, L; Francillon, A; Le Feuvre, C; Muller, M; Peuplier, P; Poggi, L; Renucci, JF,
)
0.54
" Good response was noted in corinfar-retard combination with Cordanum in patients with moderate hemodynamic changes, hypertonicity of sympathoadrenal system, tachycardia."( [The clinical efficacy of Korinfar-retard in combination with Cordanum, triampur and Capoten in patients with arterial hypertension].
Chil'tsov, VV; Ignat'ev, VG; Kukes, VG; Pavlov, SS; Pavlova, LI; Privalov, AN; Rumiantsev, AS, 1996
)
0.29
" Candesartan cilexetil was well tolerated both alone and in combination with the other agents."( Pharmacokinetic drug interaction studies with candesartan cilexetil.
Högemann, A; Jonkman, JH; Lins, R; Sennewald, R; van Heiningen, PN; van Lier, JJ, 1997
)
0.3
"To compare candesartan cilexetil and lisinopril in fixed combination with hydrochlorothiazide with respect to antihypertensive efficacy and tolerability."( Comparison of the AT1-receptor blocker, candesartan cilexetil, and the ACE inhibitor, lisinopril, in fixed combination with low dose hydrochlorothiazide in hypertensive patients.
Istad, H; Keinänen-Kiukaanniemi, S; McInnes, GT; O'Kane, KP; Van Mierlo, HF, 2000
)
0.74
"5 mg/kg/day) combined with indapamide (0."( Protective effects of delapril combined with indapamide or hydrochlorothiazide in spontaneously hypertensive stroke-prone rats: a comparative dose-response analysis.
Agnati, LF; Biagini, G; Boschi, S; Torri, C; Vantaggiato, G; Zini, I; Zoli, M, 2000
)
0.55
"This multicenter study evaluated the efficacy of candesartan cilexetil, an angiotensin II type 1 receptor antagonist, used alone or in combination with amlodipine or in combination with amlodipine and hydrochlorothiazide in the treatment of patients with moderate-to-severe essential hypertension."( Efficacy of candesartan cilexetil alone or in combination with amlodipine and hydrochlorothiazide in moderate-to-severe hypertension. UK and Israel Candesartan Investigators.
Antonios, TF; He, FJ; MacGregor, GA; Viskoper, JR, 2000
)
0.72
"The purpose of this study was to assess the antihypertensive efficacy and safety of losartan alone and in combination with hydrochlorothiazide (HCTZ) in African American adults with mild to moderate hypertension."( Antihypertensive efficacy and safety of losartan alone and in combination with hydrochlorothiazide in adult African Americans with mild to moderate hypertension.
Alderman, M; Alexander, J; Ceesay, P; Espenshade, M; Flack, JM; Goldberg, A; Gradman, A; Green, S; Kraus, WE; Lester, FM; Pratt, JH; Saunders, E; Vargas, R, 2001
)
0.75
" This article reviews the safety and tolerability of eprosartan in combination with hydrochlorothiazide from 17 studies of 1899 patients with hypertension and normotensive volunteers."( Safety and tolerability of eprosartan in combination with hydrochlorothiazide.
Böhm, M; Sachse, A, 2002
)
0.78
" The results suggest that hydrochlorothiazide does not interact in the fixed combination with the pharmacokinetics of spirapril and vice versa."( Drug interaction of spirapril hydrochloride monohydrate and hydrochlorothiazide. A clinical study to compare the pharmacokinetics after administration of spirapril hydrochloride monohydrate tablets, hydrochlorothiazide tablets and fixed combination bi-lay
Amschler, S; Erb, K; Hermann, R; Junge, K; Krupp, S; Schäfer, HF; Schulz, HU; Schürer, M, 2003
)
0.86
" We aimed to clarify the effects of losartan and its combination with hydrochlorothiazide on 24-h blood pressures (BPs), central hemodynamics and microcirculation in essential hypertension (EH)."( Central and peripheral hemodynamic effects of losartan and in combination with hydrochlorothiazide in mild to moderate essential hypertension.
Bulatov, VA; Os, I; Podzolkov, VI; Son, EA, 2003
)
0.78
"Forty patients with mild to moderate EH were randomly allocated to receive losartan 50 mg (group I) or losartan 50 mg in combination with hydrochlorothiazide, 12."( Central and peripheral hemodynamic effects of losartan and in combination with hydrochlorothiazide in mild to moderate essential hypertension.
Bulatov, VA; Os, I; Podzolkov, VI; Son, EA, 2003
)
0.75
" Losartan and its combination with hydrochlorothiazide improved main parameters of microcirculation."( Central and peripheral hemodynamic effects of losartan and in combination with hydrochlorothiazide in mild to moderate essential hypertension.
Bulatov, VA; Os, I; Podzolkov, VI; Son, EA, 2003
)
0.82
"Losartan monotherapy and losartan in combination with hydrochlorothiazide are effective antihypertensive agents."( Central and peripheral hemodynamic effects of losartan and in combination with hydrochlorothiazide in mild to moderate essential hypertension.
Bulatov, VA; Os, I; Podzolkov, VI; Son, EA, 2003
)
0.79
"The aim of this study was to compare the time-effect profiles of a once-daily administration of valsartan and amlodipine, each given alone or in combination with hydrochlorothiazide, in terms of ambulatory blood pressure (BP) and heart rate in elderly patients with isolated systolic hypertension."( Comparison of the effects on 24-h ambulatory blood pressure of valsartan and amlodipine, alone or in combination with a low-dose diuretic, in elderly patients with isolated systolic hypertension (Val-syst Study).
Ambrosia, GB; Caiazza, A; Malacco, E; Mugellini, A; Palatini, P; Santonastaso, M; Spagnuolo, V, 2004
)
0.52
"The present study investigates the effects of chronic administration of ACEIs (angiotensin-converting-enzyme inhibitors; either zofenopril or enalapril) in combination with a diruetic (hydrochlorothiazide) on BP (blood pressure) increase and renal injury induced by L-NAME (NG-nitro-L-arginine methyl ester), an inhibitor of NO (nitric oxide) synthesis."( Effects of angiotensin-converting-enzyme inhibitors in combination with diuretics on blood pressure and renal injury in nitric oxide-deficiency-induced hypertension in rats.
Alcaraz, A; Atucha, NM; Evangelista, S; García-Estañ, J; Navarro, EG; O'Valle, F; Ortiz, MC; Vargas, F, 2006
)
0.52
"To attain recent goals of blood pressure (BP) control, multiple drug therapy combinations are required, including higher doses of thiazide diuretics in combination with other classes of antihypertensive drug therapy."( Effects of the angiotensin II receptor blockers telmisartan vs valsartan in combination with hydrochlorothiazide 25 mg once daily for the treatment of hypertension.
Davidai, G; Koval, SE; Murwin, D; Neutel, JM; Punzi, HA; White, WB, 2006
)
0.55
" Its antihypertensive efficacy and safety, alone and in combination with hydrochlorothiazide (HCTZ), were investigated in an 8-week, double-blind, placebo-controlled trial in hypertensive patients."( Renin inhibition with aliskiren provides additive antihypertensive efficacy when used in combination with hydrochlorothiazide.
Calhoun, D; Chrysant, SG; Hsu, H; Matrisciano-Dimichino, L; Schober, B; Villamil, A; Zhang, J, 2007
)
0.78
"Aliskiren monotherapy demonstrated significant BP lowering, and its effect was considerably greater when combined with HCTZ."( Renin inhibition with aliskiren provides additive antihypertensive efficacy when used in combination with hydrochlorothiazide.
Calhoun, D; Chrysant, SG; Hsu, H; Matrisciano-Dimichino, L; Schober, B; Villamil, A; Zhang, J, 2007
)
0.55
" In 3 open-label studies in which blood pressure was assessed with ambulatory measurement, aliskiren was administered to patients with mild-to-moderate hypertension in combination with hydrochlorothiazide (n=23), ramipril (n=21), or irbesartan (n=23)."( Aliskiren reduces blood pressure and suppresses plasma renin activity in combination with a thiazide diuretic, an angiotensin-converting enzyme inhibitor, or an angiotensin receptor blocker.
Barton, J; Dicker, P; Jensen, C; Mulcahy, D; Nussberger, J; O'Brien, E; Stanton, A, 2007
)
0.53
" We investigated the blood pressure (BP)-lowering effects of the oral direct renin inhibitor aliskiren, alone or in combination with the angiotensin receptor blocker valsartan."( Aliskiren, an orally effective renin inhibitor, provides antihypertensive efficacy alone and in combination with valsartan.
Aldigier, JC; Azizi, M; Chiang, Y; Januszewicz, A; Pool, JL; Satlin, A; Schmieder, RE; Zidek, W, 2007
)
0.34
" When using combination therapy, antihypertensive agents with complementary mechanisms of action are recommended, for example, an angiotensin receptor blocker (ARB) in combination with hydrochlorothiazide (HCTZ), a beta-blocker + HCTZ, an ACE inhibitor + HCTZ, or a calcium channel blocker + an ACE inhibitor."( Olmesartan medoxomil combined with hydrochlorothiazide for the treatment of hypertension.
Greathouse, M, 2006
)
0.8
"In 2004-2005, the antihypertensive effects of telmisartan 80 mg versus valsartan 160 mg combined with hydrochlorothiazide 25 mg were assessed in a large placebo-controlled trial in patients with stages 1 and 2 hypertension and demonstrated that both agents were highly effective in lowering blood pressure (BP) compared with placebo and that telmisartan lowered BP significantly greater than valsartan."( Effects of the angiotensin II receptor blockers telmisartan versus valsartan in combination with hydrochlorothiazide: a large, confirmatory trial.
Chrysant, SG; Davidai, G; Guthrie, R; Koval, SE; Murwin, D; White, WB, 2008
)
0.78
"We conclude that losartan alone or in combination with HCTZ was generally well tolerated and effective in the treatment of elevated systolic and diastolic BP in obese patients with hypertension."( A double-blind, randomized study evaluating losartan potassium monotherapy or in combination with hydrochlorothiazide versus placebo in obese patients with hypertension.
Abate, N; Chen, E; Creager, MA; Galet, V; Jia, G; Julius, S; Lerman, A; Lyle, PA; Oparil, S; Pool, J; Tershakovec, AM, 2008
)
0.56
" These results show that higher-dose thiazide diuretic in combination with T80 in patients with hypertension uncontrolled by T80/H12."( Results of increasing doses of hydrochlorothiazide in combination with an angiotensin receptor blocker in patients with uncontrolled hypertension.
Edwards, C; Neldam, S, 2008
)
0.63
" Additionally, the increased efficacy resulting from the combination with hydrochlorothiazide does not appear to significantly affect the tolerability profile of olmesartan medoxomil."( Efficacy and safety of olmesartan medoxomil alone and in combination with hydrochlorothiazide.
Punzi, HA, 2009
)
0.81
"The antihypertensive effects of telmisartan 80 mg versus valsartan 160 mg, both combined with hydrochlorothiazide (HCTZ) 25 mg, were assessed in a pooled analysis from two large trials with identical study designs in patients with stage 1-2 hypertension."( Impact of angiotensin receptor blockade in combination with hydrochlorothiazide 25 mg in 2121 patients with stage 1-2 hypertension.
Davidai, G; Schumacher, H; White, WB, 2009
)
0.81
" We recruited 10 healthy volunteers in order to study the effects of 32 g liquorice alone or in combination with 25mg hydrochlorothiazide a day for 2 weeks."( Effects of low-dose liquorice alone or in combination with hydrochlorothiazide on the plasma potassium in healthy volunteers.
Hukkanen, J; Savolainen, MJ; Ukkola, O, 2009
)
0.81
"The aim of this study was to compare the effects between calcium channel blockers and diuretics when used in combination with angiotensin II receptor blocker on aortic systolic blood pressure (BP) and brachial ambulatory systolic BP."( Differential effects between a calcium channel blocker and a diuretic when used in combination with angiotensin II receptor blocker on central aortic pressure in hypertensive patients.
Eguchi, K; Ishikawa, J; Kario, K; Matsui, Y; Miyashita, H; O'Rourke, MF; Shimada, K, 2009
)
0.35
" This antiihypertensve effect was considerably potentiated, when kardos was administered in combination with enalapril."( Pharmacodynamics of kardos administered as monotherapy and in combination with hypothiazide and enalapril in grade I-II arterial hypertension.
Bakumov, PA; Epshtein, OI; Kachanova, MV; Petrov, VI; Sabanov, LB; Sergeeva, SA; Zabolotneva, YA; Zernyukova, EA, 2009
)
0.35
"We evaluated the bioavailability of each ingredient of the Polycap and determined any drug-drug interactions relative to single component reference preparations."( Preservation of bioavailability of ingredients and lack of drug-drug interactions in a novel five-ingredient polypill (polycap): a five-arm phase I crossover trial in healthy volunteers.
Chakraborty, BS; Desai, J; Ghosh, C; Jha, V; Khamar, B; Patel, A; Shah, G; Shah, T, 2010
)
0.36
"Comparative bioavailability was computed and no drug-drug interactions and no difference in comparative bioavailability were concluded for each ingredient based on point estimates of the T/R ratio of the geometric means falling within 80-125% for peak plasma concentration (C(max)), area under the plasma concentration-time curve from time zero to the last measurable concentration (AUC(t)), and AUC from time zero to infinity (AUC(infinity))."( Preservation of bioavailability of ingredients and lack of drug-drug interactions in a novel five-ingredient polypill (polycap): a five-arm phase I crossover trial in healthy volunteers.
Chakraborty, BS; Desai, J; Ghosh, C; Jha, V; Khamar, B; Patel, A; Shah, G; Shah, T, 2010
)
0.36
" The present study in healthy volunteers establishes that Polycap is safe (no serious adverse events) and well tolerated, and that there is no indication of pharmacokinetic drug-drug interactions for any of the ingredients, with their bioavailabilities being well preserved."( Preservation of bioavailability of ingredients and lack of drug-drug interactions in a novel five-ingredient polypill (polycap): a five-arm phase I crossover trial in healthy volunteers.
Chakraborty, BS; Desai, J; Ghosh, C; Jha, V; Khamar, B; Patel, A; Shah, G; Shah, T, 2010
)
0.36
" This study evaluates irbesartan in relation to commonly used alternative hypertension therapies losartan and valsartan given in combination with hydrochlorothiazide (HCTZ) in the general hypertensive population in Greece."( Economic evaluation of irbesartan in combination with hydrochlorothiazide in the treatment of hypertension in Greece.
Ekman, M; Fragoulakis, V; Maniadakis, N; Papagiannopoulou, V; Yfantopoulos, J, 2011
)
0.82
"Based on efficacy data from clinical trials and lower attainment costs in various hypertensive patient populations, irbesartan in combination with HCTZ compares favorably with losartan and valsartan in combination with HCTZ in the Greek setting."( Economic evaluation of irbesartan in combination with hydrochlorothiazide in the treatment of hypertension in Greece.
Ekman, M; Fragoulakis, V; Maniadakis, N; Papagiannopoulou, V; Yfantopoulos, J, 2011
)
0.62
" Drug-drug interactions were investigated when nebivolol was coadministered to subjects classified as poor CYP2D6 metabolizers and extensive CYP2D6 metabolizers who were receiving other drugs commonly administered to patients with hypertension or compounds metabolized by cytochrome P450 (CYP) 2D6."( Effects of commonly administered agents and genetics on nebivolol pharmacokinetics: drug-drug interaction studies.
Gorski, JC; Lindamood, C; Ortiz, S; Rackley, R; Shaw, A, 2011
)
0.37
"Fimasartan administered alone or in combination with HCTZ was well tolerated at the described dosages."( Assessment of the drug-drug interactions between fimasartan and hydrochlorothiazide in healthy volunteers.
Cho, JY; Jang, IJ; Jeon, H; Kim, J; Lim, KS; Shin, KH; Shin, SG; Yoon, SH; Yu, KS, 2012
)
0.62
"To compare the pharmacokinetic (PK) profiles and evaluate the PK interaction of hydrochlorothiazide (HCTZ) used alone and in combination with benazepril (BENA) or valsartan (VAL) in healthy Chinese volunteers."( Pharmacokinetic profiles of hydrochlorothiazide alone and in combination with benazepril or valsartan in healthy Chinese volunteers: evaluation of the potential interaction.
Huang, Y; Jiang, J; Li, Y; Liu, H; Tian, L; Xie, S; Xu, L, 2011
)
0.89
" Overall, HCTZ alone as well as in combination with BENA and VAL was well tolerated within the scope of the current studies in Chinese health volunteers."( Pharmacokinetic profiles of hydrochlorothiazide alone and in combination with benazepril or valsartan in healthy Chinese volunteers: evaluation of the potential interaction.
Huang, Y; Jiang, J; Li, Y; Liu, H; Tian, L; Xie, S; Xu, L, 2011
)
0.66
"Previous studies have shown highly effective lowering of blood pressure with thiazide diuretics in combination with angiotensin receptor blockers."( Low dose of hydrochlorothiazide, in combination with angiotensin receptor blocker, reduces blood pressure effectively without adverse effect on glucose and lipid profiles.
Fujiwara, W; Ishii, J; Izawa, H; Kinoshita, K; Morimoto, S; Mukaide, D; Nomura, M; Ozaki, Y; Ukai, G; Yokoi, H, 2013
)
0.77
" Mean extraction recoveries of three QCs for the triple drug combination were 76."( Simple RP-HPLC method for determination of triple drug combination of valsartan, amlodipine and hydrochlorothiazide in human plasma.
Pancholi, SS; Sharma, RN, 2012
)
0.6
"To compare the effects of valsartan combined with amlodipine or hydrochlorothiazide regimen on blood pressure variation and plasma nitric oxide (NO) and endothelin (ET) in elderly hypertensive patients."( [Effects of valsartan combined with amlodipine or hydrochlorothiazide regimen on blood pressure variation in elderly hypertensive patients].
Sun, CX; Tao, CW; Wu, ZB; Yu, QG; Zhang, Y, 2012
)
0.87
"Valsartan in combination with amlodipine or hydrochlorothiazide can both effectively lower BPV in elderly hypertensive patients and improve the vascular endothelial function and the former regimen is more suitable for elderly hypertensive patients."( [Effects of valsartan combined with amlodipine or hydrochlorothiazide regimen on blood pressure variation in elderly hypertensive patients].
Sun, CX; Tao, CW; Wu, ZB; Yu, QG; Zhang, Y, 2012
)
0.89
" Aliskiren alone or in combination with HCT is safe and effective in Hispanic/Latino patients with stage 2 hypertension."( Aliskiren alone or in combination with hydrochlorothiazide in Hispanic/Latino patients with systolic blood pressure 160 mm Hg to <180 mm Hg (Aliskiren Alone or in Combination with Hydrochlorothiazide in Patients with Stage 2 Hypertension to Provide Quick
Aguirre P, F; Alessi, T; Baschiera, F; Black, HR; Wright, M, 2012
)
0.65
" PubMed searches were conducted to identify randomized trials (n = 14) comparing the two agents, alone or combined with hydrochlorothiazide."( Telmisartan or valsartan alone or in combination with hydrochlorothiazide: a review.
Lacourcière, Y, 2013
)
0.85
"The aim of the study was to estimate the efficacy of lysinopril (and/or its combination with hydrochlorothiazide) in terms of alteration of the diurnal AP profile and heart rhythm in patients with essential hypertension (EH)."( [The efficacy of lysinopril (and/or its combination with hydrochlorothiazide) in patients with essential hypertension].
Kakhramanova, SM, 2012
)
0.84
" This study provides a direct comparison of chlorthalidone with hydrochlorothiazide, each combined with the angiotensin receptor blocker azilsartan medoxomil, on blood pressure reduction and control rates."( Antihypertensive efficacy of hydrochlorothiazide vs chlorthalidone combined with azilsartan medoxomil.
Bakris, GL; Cushman, WC; Handley, A; Kupfer, S; Sica, D; Song, E; Weber, MA; White, WB, 2012
)
0.91
"Chlorthalidone combined with azilsartan medoxomil provides better blood pressure reduction and a higher likelihood of achieving blood pressure control than hydrochlorothiazide combined with azilsartan medoxomil."( Antihypertensive efficacy of hydrochlorothiazide vs chlorthalidone combined with azilsartan medoxomil.
Bakris, GL; Cushman, WC; Handley, A; Kupfer, S; Sica, D; Song, E; Weber, MA; White, WB, 2012
)
0.87
" The purpose of the study was to assess the efficacy and safety of losartan and its fixed combination with hydrochlorothiazide (HCTZ) in patients with hypertension."( [Effectiveness and safety of losartan and its combination with hydrochlorothiazide in patients with hypertension: in result study].
Glezer, MG; Saĭgitov, RT, 2012
)
0.83
" Hypertensive patients (clinic blood pressure [BP] ≥ 140/90 mmHg) received telmisartan 40 or 80 mg either alone or in combination with HCTZ 12."( The effects of telmisartan alone or in combination with hydrochlorothiazide on morning home blood pressure control: the SURGE 2 practice-based study.
Bilo, G; Parati, G; Redon, J, 2013
)
0.64
"The study is to investigate drug-drug interaction (DDI) between olmesartan medoxomil and hydrochlorothiazide (HCTZ), to confirm bioequivalence (BE) of a new combined formulation and coadministration of separate local tablets, and to receive pharmacokinetics and tolerability of the new combined formulation after multiple doses in healthy Chinese subjects."( Pharmacokinetics and tolerability of olmesartan medoxomil plus hydrochlorothiazide combination in healthy Chinese subjects: drug-drug interaction, bioequivalence, and accumulation.
Hu, P; Jiang, J; Liu, DY; Wang, CG; Zhang, JY, 2014
)
0.86
"Thus, despite the similar BP reduction the combination of ACE-inhibitor--perindopril with indapamide retard possesses more favorable vascular and metabolic effects compared to combination with hydrochlorothiazide that potentially may account for different prognosis of patients with arterial hypertension on long-term treatment."( [Direct comparison of endothelial and metabolic effects of perindopril combination with indapamide retard or hydrochlorothiazide].
Chindareva, OI; Nechaeva, GI; Pritykina, TV; Semenkin, AA; Stroeva, TV; Zhenatov, AB; Zhivilova, LA, 2014
)
0.8
" In 3 separate studies, pharmacokinetic drug-drug interactions (DDIs) potential was assessed when LCZ696 was coadministered with hydrochlorothiazide (HCTZ), amlodipine, or carvedilol."( Pharmacokinetic drug-drug interaction assessment between LCZ696, an angiotensin receptor neprilysin inhibitor, and hydrochlorothiazide, amlodipine, or carvedilol.
Greeley, M; Hsiao, HL; Langenickel, TH; Pal, P; Rajman, I; Rebello, S; Roberts, J; Sunkara, G; Zhou, W, 2015
)
0.83
"The present study deals with the application of mechanochemical approach for the preparation of drug-drug multicomponent solid forms of three poorly soluble antihypertensive drugs (telmisartan, irbesartan and hydrochlorothiazide) using atenolol as a coformer."( Drug-Drug Multicomponent Solid Forms: Cocrystal, Coamorphous and Eutectic of Three Poorly Soluble Antihypertensive Drugs Using Mechanochemical Approach.
Chadha, R; Haneef, J, 2017
)
0.64
" After one week of washout in previously treated patients, 74 subjects were treated with valsartan or valsartan combined with HCTZ for 16 weeks according to the protocol."( The efficacy and safety of valsartan and a combination of valsartan and hydrochlorothiazide in the treatment of patients with mild to moderate arterial hypertension: a subgroup analysis of the effect of valsartan and its combination with….
Accetto, R; Barbic Zagar, B; Sirenko, Y; Vincelj, J; Widimsky, J; Yevgenyevna, IC, 2018
)
0.71
"To observe and analyze the clinical efficacy and ultrasound detection results of treatment of hypertensive patients with heart disease with valsartan combined with hydrochlorothiazide."( Clinical efficacy and ultrasound inspection of the treatment of hypertensive heart patients with Valsartan combined with hydrochlorothiazide.
Dai, M; Qian, D; Tao, H; Zhang, C, 2018
)
0.88
"To build a physiologically based pharmacokinetic (PBPK) model for fimasartan, amlodipine, and hydrochlorothiazide, and to investigate the drug-drug interaction (DDI) potentials."( Physiologically Based Pharmacokinetic Modeling of Fimasartan, Amlodipine, and Hydrochlorothiazide for the Investigation of Drug-Drug Interaction Potentials.
Jeon, I; Kim, E; Lee, HA; Lee, S; Rhee, SJ; Song, IS; Yu, KS, 2018
)
0.93
" The third-generation liphophilic angiotensin converting enzyme inhibitor zofenopril, administered alone or combined with a thiazide diuretic, has proved to be effective in lowering blood pressure in hypertensive patients and to reduce the risk of fatal and non-fatal events in post-acute myocardial infarction and heart failure."( Efficacy of Zofenopril Alone or in Combination with Hydrochlorothiazide in Patients with Kidney Dysfunction.
Borghi, C; Omboni, S, 2019
)
0.76
" Participants were divided into six treatment groups based on the hypertensive drug therapy they were using; lisinopril, losartan or valsartan alone or in combination with hydrochlorothiazide (A, B and C group respectively) or combination of lisinopril, losartan or valsartan with/without hydrochlorothiazide together with amlodipine (D, E and F respectively)."( Effects of Different Antihypertensive Drug Combinations on Blood Pressure and Arterial Stiffness.
Hebibovic, S; Jatic, Z; Rustempasic, E; Skopljak, A; Sukalo, A; Valjevac, A, 2019
)
0.71
"These data suggest that lisinopril/lisinopril + hydrochlorothiazide, losartan/losartan + hydrochlorothiazide and valsartan/valsartan + hydrochlorothiazide alone or in combination with amlodipine are equally effective and well tolerated for the reduction of both systolic and diastolic blood pressure and improve arterial stiffness in patients with essential hypertension."( Effects of Different Antihypertensive Drug Combinations on Blood Pressure and Arterial Stiffness.
Hebibovic, S; Jatic, Z; Rustempasic, E; Skopljak, A; Sukalo, A; Valjevac, A, 2019
)
0.77
" This trial aims to investigate the efficacy of chlorthalidone and hydrochlorothiazide, in combination with amiloride at different doses, for initial management of patients with primary hypertension."( Efficacy of chlorthalidone and hydrochlorothiazide in combination with amiloride in multiple doses on blood pressure in patients with primary hypertension: a protocol for a factorial randomized controlled trial.
Bottino, LG; Ferrari, F; Fuchs, FD; Fuchs, SC; Helal, L; Martins, VM, 2019
)
1.04
" Chlorthalidone and hydrochlorothiazide, in combination with amiloride in multiple doses, will be tested in terms of blood pressure lowering efficacy and safety."( Efficacy of chlorthalidone and hydrochlorothiazide in combination with amiloride in multiple doses on blood pressure in patients with primary hypertension: a protocol for a factorial randomized controlled trial.
Bottino, LG; Ferrari, F; Fuchs, FD; Fuchs, SC; Helal, L; Martins, VM, 2019
)
1.12
" The proposed methods were applied to two pharmaceutical formulations; the method for HCT and AMH has proven as reliable assaying method, whereas the method for TML, when combined with HCT, is applicable to screening semi-quantitative analyses."( Simultaneous spectrofluorometric analysis of tablets containing hydrochlorothiazide combined with timolol maleate or amiloride hydrochloride.
Lataifeh, A; Mohammed, MS; Wedian, F, 2020
)
0.8
" In this study, we evaluated the efficacy of firibastat in combination with enalapril, an angiotensin I-converting enzyme inhibitor, and hydrochlorothiazide (HCTZ), in conscious hypertensive deoxycorticosterone acetate (DOCA)-salt rats, which display high plasma arginine-vasopressin levels, low circulating renin levels and resistance to treatment by systemic RAS blockers."( Effects of firibastat in combination with enalapril and hydrochlorothiazide on blood pressure and vasopressin release in hypertensive DOCA-salt rats.
Balavoine, F; De Mota, N; Hmazzou, R; Llorens-Cortes, C; Marc, Y, 2021
)
1.07
"This study aimed to probe the effects of low-dose irbesartan and hydrochlorothiazide in combination with levamlodipine at different times on the circadian rhythm of blood pressure, matrix metalloproteinases (MMPs), and tissue inhibitors of metalloproteinases (TIMPs) levels in patients with non-dipper hypertension (NDH)."( Effect of administration of low-dose irbesartan and hydrochlorothiazide combined with levamlodipine at different times on the circadian rhythm of blood pressure and the levels of MMPs and TIMPs in non-dipper patients with grade 1 and 2 hypertension.
Chen, J; Dong, G; Ge, M; Liu, H; Luo, Y; Wang, J; Yan, P; Zhang, J, 2023
)
1.4
" The availability of OM combined with HCTZ, AML or both at different dosages makes it a valuable option to customize therapy based on the levels of BP and the clinical characteristics of hypertensive patients."( Single-Pill Combination with Three Antihypertensive Agents to Improve Blood Pressure Control in Hypertension: Focus on Olmesartan-Based Combinations.
Burnier, M; Redon, J; Volpe, M, 2023
)
0.91
" To conclude, beta-glucan alone and in combination with hydrochlorothiazide may be a promising a strategy for managing hypertension and related cardiac complications."( Oat Beta-Glucan Alone and in Combination with Hydrochlorothiazide Lowers High Blood Pressure in Male but Not Female Spontaneously Hypertensive Rats.
Malunga, L; Netticadan, T; Raj, P; Sabra, A; Sayfee, K; Thandapilly, SJ; Wijekoon, C; Yu, L, 2023
)
1.41

Bioavailability

Experiments have been carried out in dogs and man to determine the effect of hydrochlorothiazide (HCT) on the pharmacokinetics of propranolol.

ExcerptReferenceRelevance
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51
" Cumulative urinary excretion data from test capsule preparations showed that bioavailability was enhanced by the presence of PVP."( The influence of polyvinylpyrrolidone on the solution and bioavailability of hydrochlorothiazide.
Corrigan, OI; Timoney, RF; Whelan, MJ, 1976
)
0.48
" This pH-dependent release characteristic may not correspond to a change in bioavailability in all cases, but it represents a potential problem which should be considered by the formulator."( PH-dependent drug release from certain commercial tablets.
Lach, JL; Sutton, JE; Wagner, RS, 1977
)
0.26
" Metoprolol did not significantly influence the bioavailability or the time-course of HCT."( Bioavailability and disposition of metoprolol and hydrochlorothiazide combined in one tablet and of separate doses of hydrochlorothiazide.
Johnsson, G; Jordö, L; Lundborg, P; Persson, BA; Regärdh, CG; Rönn, O, 1979
)
0.51
" However, the bioavailability of the two brands of hydrochlorothiazide did not differ significantly as judged by comparison of the AUC0 leads to 9h and AUC0 leads to chi, and the urinary recovery of hydrochlorothiazide during 48 hrs."( Bioavailability of two hydrochlorothiazide preparations.
Beermann, B; Groschinsky-Grind, M; Lindstrom, B, 1977
)
0.82
" The method was sufficiently sensitive for hydrochlorothiazide bioavailability studies and also was applicable for the determination of whole blood drug levels."( Determination of plasma hydrochlorothiazide levels in humans.
Redalieu, E; Tipnis, VV; Wagner, WE, 1978
)
0.83
"Tablet formulations of spironolactone with hydrochlorothiazide were studied in vitro and in vivo to evaluate the effect of formulation parameters on the bioavailability of spironolactone."( In vitro and in vivo availability of spironolactone from oral dosage forms.
Chao, AY; Karim, A; Mattes, K; Nicholova, B; Sanvordeker, DR; Zagarella, J, 1976
)
0.52
" We found that salicylic acid absorption from this solution was delayed but complete whereas the absorption of atenolol, cimetidine, frusemide and hydrochlorothiazide was four- to five-fold lower than expected from oral bioavailability studies."( Absorption of polar drugs following caecal instillation in healthy volunteers.
Kim, M; Riley, SA; Rowland, M; Sutcliffe, F; Turnberg, LA, 1992
)
0.48
" Relative bioavailability of the FR and SR formulations were 82 and 41%, respectively, compared to the commercial tablet."( In vitro/in vivo evaluation of hydrochlorothiazide in experimental hydrochlorothiazide/triamterene combination tablets in beagle dogs.
Lipps, D; Ritschel, WA; Sakr, A; Turkoglu, M; Warner, A, 1991
)
0.57
" The second study (II) assessed the bioavailability of the new product given as a single tablet on two occasions separated by an interval of 12 h compared to the full-strength product given as a single dose."( Absorption and disposition of a new low-dose combination formulation of hydrochlorothiazide and triamterene.
Benet, LZ; Blume, CD; Liang-Gee, W; Lin, ET; Williams, RL, 1990
)
0.51
"5 mg of triamterene) to one capsule of Dyazide (25 mg of hydrochlorothiazide and 50 mg of triamterene) to determine if the difference in bioavailability would be reflected in differences in blood pressure control and metabolic changes."( A comparison of the anti-hypertensive effectiveness of two triameterene/hydrochlorothiazide combinations: Maxzide versus Dyazide.
Casner, PR; Dillon, KR, 1990
)
0.76
" Parent drug absorption and diacid bioavailability in the rat were higher than for enalapril, and the inhibition of plasma ACE of longer duration."( Biological properties of the angiotensin-converting enzyme inhibitor cilazapril.
Brewster, M; Budd, J; Francis, RJ; Klevans, LR; Natoff, IL; Nixon, JS; Patel, AT; Wenger, J; Worth, E,
)
0.13
"The clinical efficacy, safety, and bioavailability of a generic triamterene-hydrochlorothiazide product were compared with those of Dyazide."( Comparative efficacy and bioequivalence of a brand-name and a generic triamterene-hydrochlorothiazide combination product.
Cane, RC; Costello, K; Goodwin, P; Perkal, M; Sharoky, M; Tabatznik, B, 1989
)
0.73
"The influence of non-active ingredients in the manufacture of pellets on in-vitro dissolution rate and on bioavailability of hydrochlorothiazide has been studied."( The dissolution rate and bioavailability of hydrochlorothiazide in pellet formulations.
Bogaert, M; Herman, J; Klinger, GH; Lefebvre, R; Remon, JP; Schwartz, JB, 1988
)
0.74
" T bioavailability from capsules was poorer and more variable than that from a suspension."( Oral triamterene disposition.
Hasegawa, J; Lin, ET; Sörgel, F; Williams, RL, 1985
)
0.27
" The relative bioavailability (Fr) of the combination tablet compared with guanabenz alone was 96%; thus the two formulations were bioequivalent with respect to guanabenz."( Effects of guanabenz on gastrointestinal absorption of hydrochlorothiazide.
Chiang, ST; Davis, M; Pascucci, VL; Spangler, T; Walker, BR; White, GR, 1984
)
0.51
" This reduced bioavailability may reduce its effectiveness in hypertensive patients who change from optimally bioavailable hydrochlorothiazide tablets to Dyazide capsules in an effort to correct hypokalemia."( A new antihypertensive agent: Maxzide (75 mg triamterene/50 mg hydrochlorothiazide).
Blume, CD; Williams, RL, 1984
)
0.71
" Furthermore, because of the bioavailability of the pharmaceutical formulation, the dose the patient "takes" may not be the one that he or she actually gets."( Effect of bioavailability on dose-response relationships.
Goldman, P, 1984
)
0.27
" The clinical consequences of the limited bioavailability of the active ingredients of Dyazide are discussed."( Bioequivalence study of a new tablet formulation of triamterene and hydrochlorothiazide.
Benet, LZ; Blume, CD; Lin, ET; Upton, RA; Williams, RL, 1984
)
0.5
" In contradiction to a recent publication, no interaction between the drugs affecting the bioavailability or renal clearance of either could be demonstrated."( Absence of a significant pharmacokinetic interaction between hydrochlorothiazide and triamterene when coadministered.
Benet, LZ; Blume, CD; Gee, WL; Lin, ET; Upton, RA; Williams, RL, 1984
)
0.51
" When the dose did not exceed the solubility of the drug in the intestinal lumen, the fraction absorbed depended on the transit rate relative to the absorption rate and the pK alpha relative to the pH profile, but was independent of drug dose."( Physicochemical model for dose-dependent drug absorption.
Amidon, GL; Dressman, JB; Fleisher, D, 1984
)
0.27
"The bioavailability and pharmacokinetics of 10 mg of mepindolol sulphate and of 25 mg of hydrochlorothiazide were compared in a cross-over design in five healthy volunteers after the administration of either the single drugs (Corindolan and Esidrix) or in combination (Tenesor)."( Pharmacokinetics of mepindolol administered alone and in combination with hydrochlorothiazide--a bioequivalence study.
Krause, W; Lennert, C,
)
0.58
" A pilot bioavailability study was carried out in four normal healthy male volunteers."( Preliminary observations on dissolution and bioavailability of triamterene-hydrochlorothiazide combination products.
Cabana, BE; Knapp, G; Lin, J; Prasad, VK; Shah, VP; Walker, MA,
)
0.36
"The bioavailability of hydrochlorothiazide was determined following single oral 25-, 50-, 100-, and 200-mg tablet and suspension doses in 12 healthy male volunteers."( Bioavailability of hydrochlorothiazide from tablets and suspensions.
Patel, RB; Patel, UR; Prasad, VK; Rogge, MC; Selen, A; Shah, VP; Welling, PG, 1984
)
0.91
"A pilot bioavailability study was carried out where two subjects each were administered a dose of 25, 50 or 100 mg of commercially available hydrochlorothiazide (HCT) tablets."( Thiazides III. Evidence of dose proportionality of hydrochlorothiazide 25, 50 and 100 mg tablets.
Cabana, BE; Hunt, JP; Lee, JJ; Prasad, VK; Shah, VP, 1983
)
0.72
"The bioavailability of hydrochlorothiazide from 50-mg oral tablet doses was examined in healthy male volunteers under fasting and nonfasting conditions."( Pharmacokinetics of hydrochlorothiazide in fasted and nonfasted subjects: a comparison of plasma level and urinary excretion methods.
Barbhaiya, RH; Corrick-West, HP; Craig, WA; Welling, PG, 1982
)
0.9
"Experiments have been carried out in dogs and man to determine the effect of hydrochlorothiazide (HCT) on the pharmacokinetics of propranolol and to evaluate the bioavailability of two dosage forms containing both propranolol and HCT (40/25 and 80/25 mg, respectively)."( Biopharmaceutical characteristics of a new propranolol/hydrochlorothiazide tablet combination.
Dubuc, J; Dvornik, D; Kraml, M; Lee, TY; Mullane, J; Patterson-Kreuscher, S; Perdue, H,
)
0.61
" The bioavailability of oral allopurinol computed from plasma data was 90."( Kinetics of allopurinol after single intravenous and oral doses. Noninteraction with benzbromarone and hydrochlorothiazide.
Breithaupt, B; Tittel, M, 1982
)
0.48
"In a single-blind, randomized cross-over study the bioavailability of Spironothiazid (50 mg spironolactone, 50 mg hydrochlorothiazide) was investigated in six healthy male volunteers by comparing the same dose of the well-established drugs Aldactone dragees, 50 mg, and Esidrex tablets, 25 mg."( The bioavailability of spironolactone hydrochlorothiazide combination preparation.
Hitzenberger, G; Horwatitsch, H; Rameis, H, 1982
)
0.75
"The bioavailability and pharmacokinetics of two hydrochlorothiazide products were compared following single 50 mg oral doses to 20 healthy male volunteers."( Comparative bioavailability and pharmacokinetics of hydrochlorothiazide from oral tablet dosage forms, determined by plasma level and urinary excretion methods.
Barbhaiya, RH; Corrick-West, HP; Joslin, RS; Patel, RB; Welling, PG,
)
0.64
"In a study on the bioavailability of triamterene and hydrochlorothiazide from 3 diuretics, preparation A (25 mg hydrochlorothiazide), preparation B (50 mg triamterene) and preparation C (combination of hydrochlorothiazide and triamterene), the data for tmax, Cmax, AUC and the cumulative urine excretion were determined in 7 healthy volunteers."( [On the bioavailability of hydrochlorothiazide and triamterene from commercial drugs (author's transl)].
Knauf, H; Möhrke, W; Mutschler, E; Völger, KD, 1980
)
0.81
" The results show that the presence of both diuretics increased the intestinal absorption rate constant and the percentage diffused of propranolol hydrochloride."( In vitro detection of possible in vivo drug interactions. Part 1. The effect of hydrochlorothiazide and frusemide on the in vitro absorption characteristics of propranolol hydrochloride.
Al-Janabi, II; Anber, SA; Mustafa, RM; Razzo, FN, 1981
)
0.49
" Bioavailability of Hct showed considerable intra- and interindividual variation (32--87% and 42--77% respectively), but phenytoin did not influence the disposition parameters of the diuretic."( Disposition of hydrochlorothiazide (Hct) during phenytoin (Ph) treatment.
Brennes, M; Hoppe-Seyler, G; Keller, E; Schollmeyer, P; Sulzer, U, 1981
)
0.62
" Co-administration of candesartan cilexetil with HCTZ produced a statistically significant increase in the bioavailability and Cmax values for candesartan (18% and 25%, respectively)."( Pharmacokinetic drug interaction studies with candesartan cilexetil.
Högemann, A; Jonkman, JH; Lins, R; Sennewald, R; van Heiningen, PN; van Lier, JJ, 1997
)
0.3
"The quantitative structure-bioavailability relationship of 232 structurally diverse drugs was studied to evaluate the feasibility of constructing a predictive model for the human oral bioavailability of prospective new medicinal agents."( QSAR model for drug human oral bioavailability.
Topliss, JG; Yoshida, F, 2000
)
0.31
" The absolute bioavailability of the drug from the liquisolid tablets was 15% higher than that from the commercial one."( In vivo evaluation of hydrochlorothiazide liquisolid tablets in beagle dogs.
Asiri, YA; El-Sayed, YM; Khaled, KA, 2001
)
0.63
" Bioavailability was evaluated on the basis of plasma concentrations of enalapril and its main active metabolite, enalaprilat and hydrochlorothiazide."( Comparative bioavailability of two immediate release tablets of enalapril/hydrochlorothiazide in healthy volunteers.
Caturla, MC; Filipe, AE; Goncalves, NJ; Maya, MT; Morais, JA; Rovira, M; Silva, NE,
)
0.57
"The bioavailability of hydrochlorothiazide (HCT) from moulded isomalt-based tablets was evaluated after oral administration of 50 mg HCT to healthy volunteers as an oral moulded tablet and as a lozenge, in comparison with a conventional tablet formulation (Dichlotride 50 mg)."( Bioavailability of hydrochlorothiazide from isomalt-based moulded tablets.
Ndindayino, F; Remon, JP; Van den Mooter, G; Vervaet, C, 2002
)
0.95
" Endothelial function [basal nitric oxide (NO) bioavailability and stimulated NO release] was examined in carotid arteries using organ bath pharmacology and in mesenteric resistance arteries using wire myography."( Comparison of the effects of omapatrilat and irbesartan/hydrochlorothiazide on endothelial function and cardiac hypertrophy in the stroke-prone spontaneously hypertensive rat: sex differences.
Beattie, E; Dominiczak, AF; Graham, D; Hamilton, C; Spiers, A, 2004
)
0.57
"The aim of the present studies, performed in two different groups of volunteers, was to compare the bioavailability of 20 mg lisinopril tablets (Sinopryl as test and an orignator product as reference formulation; study 1) and lisinopril/hydrochlorothiazide (20 mg/12."( Effect of the combination of lisinopril and hydrochlorothiazide on the bioequivalence of tablet formulations.
Alpan, RS; Erenmemisoglu, A; Koytchev, R; Ozalp, Y; van der Meer, MJ, 2004
)
0.77
"Two trials were performed in different groups of volunteers with the aim to compare the bioavailability of 50 mg losartan tablets (Sarvas as test and an originator product as reference formulation; study 1) and losartan/hydrochlorothiazide (50 mg/12."( Combination of losartan and hydrochlorothiazide: in vivo bioequivalence.
Alpan, RS; Erenmemisoglu, A; Koytchev, R; Ozalp, Y; van der Meer, MJ, 2004
)
0.8
" The validated method has been successfully used to analyze human plasma samples for application in pharmacokinetic, bioavailability or bioequivalence studies."( Sensitive liquid chromatography-tandem mass spectrometry method for quantification of hydrochlorothiazide in human plasma.
Koteshwara, M; Manoj, S; Ramakrishna, NV; Varma, DP; Vishwottam, KN; Wishu, S, 2005
)
0.55
" The relative bioavailability of two FDA approved (Orange Book AB rating) solid oral dosage forms of metoprolol and propranolol/hydrochlorothiazide (combination tablets) was evaluated in human volunteers under fed conditions using a two-way crossover design."( The effect of food on the relative bioavailability of rapidly dissolving immediate-release solid oral products containing highly soluble drugs.
Asafu-Adjaye, E; Ciavarella, AB; Conner, DP; Faustino, PJ; Hussain, AS; Lesko, LJ; Mehta, MU; Parekh, A; Straughn, AB; Yang, Y; Yu, LX,
)
0.34
" The bioavailability of pellets (containing 50 mg hydrochlorothiazide) was determined after oral administration to 6 dogs."( Immediate release of poorly soluble drugs from starch-based pellets prepared via extrusion/spheronisation.
Dukić-Ott, A; Foreman, P; Remon, JP; Vervaet, C, 2007
)
0.59
" We suggest that potassium depletion and hyperuricemia in rats exacerbates endothelial dysfunction and lowers the bioavailability of nitric oxide, which blocks insulin activity and causes insulin resistance during thiazide usage."( Thiazide diuretics exacerbate fructose-induced metabolic syndrome.
Johnson, RJ; Mu, W; Nakagawa, T; Reungjui, S; Roncal, CA; Sirivongs, D; Srinivas, TR, 2007
)
0.34
" Human oral bioavailability is an important pharmacokinetic property, which is directly related to the amount of drug available in the systemic circulation to exert pharmacological and therapeutic effects."( Hologram QSAR model for the prediction of human oral bioavailability.
Andricopulo, AD; Moda, TL; Montanari, CA, 2007
)
0.34
" The pharmacokinetic studies show that GH increases the bioavailability and half-life, along with decrease in clearance and elimination rate of HCTZ when administered orally."( The potential for interaction of hydrochlorothiazide with garlic in rats.
Asdaq, SM; Inamdar, MN, 2009
)
0.63
" Meanwhile, the combination also promoted the absorption rate and the bioavailability, prolonged the action time and the accumulation time of hydrochlorothiazide in vivo."( [Pharmacokinetics of puerarin and hydrochlorothiazide from maijunan tablets in rats].
Chen, Y; Du, P; Han, FM; Zhang, X, 2009
)
0.83
"We evaluated the bioavailability of each ingredient of the Polycap and determined any drug-drug interactions relative to single component reference preparations."( Preservation of bioavailability of ingredients and lack of drug-drug interactions in a novel five-ingredient polypill (polycap): a five-arm phase I crossover trial in healthy volunteers.
Chakraborty, BS; Desai, J; Ghosh, C; Jha, V; Khamar, B; Patel, A; Shah, G; Shah, T, 2010
)
0.36
"The bioavailability of the ingredients of the Polycap (T; test) when formulated as a single capsule was compared with that of identical capsules with each of its ingredients administered separately (R; reference) in a five-arm, randomized, single-dose, two-period, two-treatment, two-sequence, crossover trial with at least a 2-week washout period in a total of 195 healthy volunteers."( Preservation of bioavailability of ingredients and lack of drug-drug interactions in a novel five-ingredient polypill (polycap): a five-arm phase I crossover trial in healthy volunteers.
Chakraborty, BS; Desai, J; Ghosh, C; Jha, V; Khamar, B; Patel, A; Shah, G; Shah, T, 2010
)
0.36
"Comparative bioavailability was computed and no drug-drug interactions and no difference in comparative bioavailability were concluded for each ingredient based on point estimates of the T/R ratio of the geometric means falling within 80-125% for peak plasma concentration (C(max)), area under the plasma concentration-time curve from time zero to the last measurable concentration (AUC(t)), and AUC from time zero to infinity (AUC(infinity))."( Preservation of bioavailability of ingredients and lack of drug-drug interactions in a novel five-ingredient polypill (polycap): a five-arm phase I crossover trial in healthy volunteers.
Chakraborty, BS; Desai, J; Ghosh, C; Jha, V; Khamar, B; Patel, A; Shah, G; Shah, T, 2010
)
0.36
" It compares the bioavailability of these two study drugs from a TDDS with conventional immediate release oral tablets in healthy volunteers."( Randomised, cross-over, comparative bioavailability trial of matrix type transdermal drug delivery system (TDDS) of carvedilol and hydrochlorothiazide combination in healthy human volunteers: a pilot study.
Aggarwal, A; Agrawal, SS, 2010
)
0.57
" To show the importance of physicochemical properties, the classic QSAR and CoMFA of neonicotinoids and prediction of bioavailability of pesticides in terms of membrane permeability in comparison with drugs are described."( Importance of physicochemical properties for the design of new pesticides.
Akamatsu, M, 2011
)
0.37
" Statistical comparison showed that the test and reference products were bioequivalent in terms of both the rate and extent of bioavailability of both active ingredients."( Bioequivalence evaluation of a triamterene-hydrochlorothiazide generic product: a new bioequivalence index for fixed-dose combinations.
Azimi, K; Hamidi, M; Shahbazi, MA, 2011
)
0.63
"The bioavailability of two 300 mg irbesartan (CAS 138402-11-6)/12."( Comparative bioavailability of two irbesartan/hydrochlorothiazide tablet formulations in Indonesian healthy subjects.
Harahap, Y; Lusthom, W; Meliala, RS; Prasaja, B; Sasongko, L; Setiawan, EC, 2010
)
0.62
" Its poor aqueous solubility is one of the reasons for its limited bioavailability after oral administration."( Pharmaceutical composition of hydrochlorothiazide:β-cyclo-dextrin: preparation by three different methods, physico-chemical characterization and in vivo diuretic activity evaluation.
Pires, MA; Sinisterra, RD; Souza Dos Santos, RA, 2011
)
0.66
"BENA decreased the bioavailability of HCTZ in Chinese healthy volunteers while VAL greatly increased the concentration of HCTZ in plasma during coadministration."( Pharmacokinetic profiles of hydrochlorothiazide alone and in combination with benazepril or valsartan in healthy Chinese volunteers: evaluation of the potential interaction.
Huang, Y; Jiang, J; Li, Y; Liu, H; Tian, L; Xie, S; Xu, L, 2011
)
0.66
" A potential reason for this is reduced nitric oxide bioavailability in African Americans, resulting in increased prevalence of factors that contribute to ventricular dysfunction."( Vascular effects of nebivolol added to hydrochlorothiazide in African Americans with hypertension and echocardiographic evidence of diastolic dysfunction: the NASAA study.
Bhaheetharan, S; Ferdinand, KC; Haque, T; Harris, J; Khan, BV; Merchant, N; Rahman, ST; Umar, K; Wahi, J, 2012
)
0.65
" Furthermore, improvement in endothelial function and increased nitric oxide bioavailability suggests a potential mechanism of efficacy of nebivolol in these patients."( Vascular effects of nebivolol added to hydrochlorothiazide in African Americans with hypertension and echocardiographic evidence of diastolic dysfunction: the NASAA study.
Bhaheetharan, S; Ferdinand, KC; Haque, T; Harris, J; Khan, BV; Merchant, N; Rahman, ST; Umar, K; Wahi, J, 2012
)
0.65
"This study was aimed to investigate the relative bioavailability of fixed-dose-combination (FDC) product of amlodipine, telmisartan and hydrochlorothiazide with individual marketed products in healthy male volunteers."( A comparative pharmacokinetic study of a fixed dose combination for essential hypertensive patients: a randomized crossover study in healthy human volunteers.
Biswas, E; Choudhury, H; Ghosh, B; Gorain, B; Halder, D; Pal, TK; Sarkar, AK; Sarkar, P, 2013
)
0.59
"The authors investigated the relative bioavailability under a fasting state of the 3 drugs in a randomized, open-label, 2-treatment, 2-period, 2-sequence, crossover bioequivalence study with a washout period of 21 days."( A comparative pharmacokinetic study of a fixed dose combination for essential hypertensive patients: a randomized crossover study in healthy human volunteers.
Biswas, E; Choudhury, H; Ghosh, B; Gorain, B; Halder, D; Pal, TK; Sarkar, AK; Sarkar, P, 2013
)
0.39
"Randomized, open-label, crossover, bioavailability studies were conducted separately in healthy Asian Indian and Japanese volunteers."( Pharmacokinetic comparison and bioequivalence evaluation of losartan/ hydrochlorothiazide tablet between Asian Indian and Japanese volunteers.
Jain, R; Khuroo, A; Kumar, S; Kurachi, K; Monif, T; Reyar, S; Singla, AK, 2014
)
0.64
"The results of these bioavailability studies indicate that the test formulation of losartan/hydrochlorothiazide 50 + 12."( Pharmacokinetic comparison and bioequivalence evaluation of losartan/ hydrochlorothiazide tablet between Asian Indian and Japanese volunteers.
Jain, R; Khuroo, A; Kumar, S; Kurachi, K; Monif, T; Reyar, S; Singla, AK, 2014
)
0.86
" The influence of TCMs on the pharmacokinetics and bioavailability of HCT was also studied to reveal the possible interaction in vivo."( Enhanced absorption and bioavailability of hydrochlorothiazide by Chinese medicines in the Zhenju antihypertensive compound.
Bai, Y; Han, L; Jing, Y; Li, Y; Qin, J; Wang, J; Wang, L, 2014
)
0.67
" The pharmacokinetic parameters and relative bioavailability were calculated, while the bioequivalence between test and reference preparations were evaluated."( [Troubleshooting of bioinequivalence of compound valsartan tablets].
Chen, XY; Shao, D; Zhan, Y; Zhang, YF; Zhong, DF, 2014
)
0.4
" Compared to a fixed-dose reference, oral co-administration of the MPT and HCT prills to dogs yielded a similar bioavailability for the HCT prills, while the MPT prills resulted in a significant higher bioavailability."( Prilling as manufacturing technique for multiparticulate lipid/PEG fixed-dose combinations.
De Beer, T; Monteyne, T; Remon, JP; Saerens, L; Vervaeck, A; Vervaet, C, 2014
)
0.4
"For the solubility and bioavailability of poorly soluble active pharmaceutical ingredients (APIs) to be improved, the transformation of crystalline APIs to the amorphous state has often been shown to be advantageous."( Predicting the Solubility Advantage of Amorphous Pharmaceuticals: A Novel Thermodynamic Approach.
Ji, Y; Paus, R; Sadowski, G; Vahle, L, 2015
)
0.42
" Here, we present the effect of food on the oral bioavailability of these two fixed dose combination tablets from two separate clinical studies in healthy subjects."( Effect of food on the oral bioavailability of amlodipine/valsartan and amlodipine/valsartan/hydrochlorothiazide fixed dose combination tablets in healthy subjects.
Ayalasomayajula, S; Jarugula, V; Jiang, X; Ligueros-Saylan, M; Reynolds, C; Serra, D; Sunkara, G; Winter, S; Zhang, Y, 2014
)
0.62
"An innovative pediatric oral formulation of hydrochlorothiazide (HCT) (2mg/mL), endowed with improved bioavailability and sustained release properties and suitable for the hypertension treatment in pediatric patients, was developed by combining the drug-cyclodextrin complexation and the incorporation of the complex into Solid Lipid Nanoparticles (SLN)."( Development and in vivo evaluation of an innovative "Hydrochlorothiazide-in Cyclodextrins-in Solid Lipid Nanoparticles" formulation with sustained release and enhanced oral bioavailability for potential hypertension treatment in pediatrics.
Cirri, M; Di Cesare Mannelli, L; Ghelardini, C; Maestrelli, F; Mennini, N; Mura, P, 2017
)
0.97
"The development of poorly water-soluble drugs faces the risk of low bioavailability and therapeutic efficacy."( Facile formation of co-amorphous atenolol and hydrochlorothiazide mixtures via cryogenic-milling: Enhanced physical stability, dissolution and pharmacokinetic profile.
Cai, B; Cai, T; Gao, Q; Huang, Y; Moinuddin, SM; Ruan, S; Shi, Q, 2017
)
0.71
"Manufacturing poorly water-soluble active pharmaceutical ingredients (API) with sufficient bioavailability is a significant challenge in pharmaceutical research."( Preparation of submicron drug particles via spray drying from organic solvents.
Dobrowolski, A; Dräger-Gillessen, JF; Pieloth, D; Schaldach, G; Strob, R; Thommes, M; Wiggers, H, 2019
)
0.51
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51
"Solubility/dissolution is said to be the key factor that influences the oral bioavailability of drug and is also the rate limiting step in formulation development."( Natural Plus Synthetic Hydrotropic Solubilization using Response Surface Methodology to Optimize the Solid Dispersion of Hydrochlorothiazide.
Nainwal, N; Saharawat, A, 2022
)
0.93
"Hydrochlorothiazide (HTZ) is a first-line drug used in the treatment of hypertension suffered from low oral bioavailability due to poor aqueous solubility and permeability."( Egg White Protein Carrier-Assisted Development of Solid Dispersion for Improved Aqueous Solubility and Permeability of Poorly Water Soluble Hydrochlorothiazide.
Jain, SP; Kharkar, PS; Pethe, AM; Telange, DR, 2021
)
2.27

Dosage Studied

The 20 mg dosage of benazepril lowered blood pressure to a degree equal to that of 25 mg hydrochlorothiazide: -12. Irbesartan therapy at a dosage of 150300 mg was instituted as monotherapy. In terms of lofexidine, there was no evidence of any adverse interactions with hydrochlorothsiazide.

ExcerptRelevanceReference
" The dissolution tests revealed that PVP retards the initial dissolution from capsule dosage forms, probably by retarding deaggregation and dispersion of drug particles."( The influence of polyvinylpyrrolidone on the solution and bioavailability of hydrochlorothiazide.
Corrigan, OI; Timoney, RF; Whelan, MJ, 1976
)
0.48
"Peripheral beta-adrenergic receptor sensitivity was characterized in 24 patients with essential hypertension and in 13 age-matched normotensive subjects using an isoproterenol hydrochloride bolus dose-response technique."( Peripheral beta-receptor responsiveness in patients with essential hypertension.
Dominic, JA; Guthrie, GP; Kotchen, TA; Love, DW; McAllister, RG, 1979
)
0.26
" Blood pressure was significantly reduced with both medications, although most patients required an increase in dosage from 250 to 500 mg ticrynafen daily."( Clinical study of ticrynafen. A new diuretic, antihypertensive, and uricosuric agent.
Freis, ED; Kyle, MC; Nemati, M, 1977
)
0.26
" Further studies are necessary to determine optimal dosage regimes and long term safety."( A double-blind comparison of the effects of hydrochlorothiazide and tienylic acid (a diuretic with uricosuric properties) in hypertension.
Gillies, AH; Morgan, TO, 1978
)
0.52
"001), but a major determinant of the magnitude of the decrease was the dosage change of the timolol."( Serum potassium and uric acid changes during treatment with timolol alone and in combination with a diuretic.
Mikkelsen, E; Pedersen, OL, 1979
)
0.26
" When warranted, dosage was increased to a maximum of 500 mg of tienilic acid and 100 mg of hydrochlorothiazide daily."( Long-term usage of tienilic acid in essential hypertension.
Beg, MA; Noble, RE, 1979
)
0.48
" The mean resting blood pressures were 168/108 mmHg, 151/98 mmHg and 150/96 mmHg at pre-trial, after the twice-daily dosage period and after the once-daily dosage period, respectively."( A fixed combination of metoprolol and hydrochlorothiazide for hypertension: a multi-centre study.
Goodfellow, RM, 1979
)
0.53
" The natriuretic action of MET was not enhanced by administration of an increased dosage (1 approximately 5 mg/kg)."( [Pharmacological study on diuretic action of 2-methyl-3-(o-tolyl)-6-sulfamyl-7-chloro-1, 2, 3, 4-tetrahydro-4-quinazolinone (metolazone) (author's transl)].
Fukuhara, A; Matsumura, Y; Morimoto, S, 1978
)
0.26
" Of the 40 unknown drug dosage form powders supplied to 10 collaborators, 39 were correctly identified."( Microcrystalline identification test of some amphetamines and hydrochlorothiazide: collaborative study.
Auerbach, L, 1978
)
0.5
" During another two-week period, a 50 mg/day dosage of hydrochlorothiazide did cause a significant rise in serum lithium levels."( Serum lithium levels and long-term diuretic use.
Jefferson, JW; Kalin, NH, 1979
)
0.51
"05 mug/ml) suitable for use with persons on therapeutic dosage levels."( GLC analysis of hydrochlorothiazide in blood and plasma.
Gruber, VF; Vandenheuvel, WJ; Walker, RW; Wolf, FJ, 1975
)
0.6
" Its effect is dosage dependent."( [Pharmacological and toxicological properties of the saluretic xipamide (4-chloro-5-sulfamoyl-2',6'-salicyloxylidide)].
Bahrmann, H; Leuschner, F; Neumann, W, 1975
)
0.25
" From the third week of treatment onwards, the Esidrix dosage was maintained; the dosage of Trasicor 80 was either maintained, increased, or later decreased, according to the results obtained."( [Ambulatory treatment of arterial hypertension urinary the new combination "saluretic and beta-sympatholytic"].
Dannhorn, R; Müller, AA, 1975
)
0.25
" An exploratory procedure based on RSM modeling is used to build a segmented linear model and a stairstep linear model to describe dose-response relationships."( The analysis of a multiple-dose, combination-drug clinical trial using response surface methodology.
Cairns, V; Koch, GG; Phillips, JA, 1992
)
0.28
" This suggests that some were apparent non-responders due to too low dosing of atenolol rather than true non-responders."( Haemodynamic findings and response rates to beta-blocker--and diuretic monotherapy in mild and moderate hypertension. A one year randomized, double blind study in 100 men.
Erikssen, J; Froeland, G; Otterstad, JE; Saltvedt, E; Soeyland, AK, 1992
)
0.28
" Therefore, after 4 weeks of washout with placebo (phase 1), doxazosin (dosage range from 1 to 16 mg, plus hydrochlorothiazide when necessary) was given to 11 essential hypertensive patients (6 M, 5 F, age range 34-63 years) for 8 weeks (phase 2) in order to achieve diastolic blood pressure values less than 90 mmHg; this dosage was then maintained for a further 20 weeks up to the end of the study (phase 3)."( Reduction of left ventricular hypertrophy after longterm antihypertensive treatment with doxazosin.
Agabiti-Rosei, E; Beschi, M; Calebich, S; Castellano, M; Muiesan, G; Muiesan, ML; Rizzoni, D; Zulli, R, 1992
)
0.5
" More patients on hydrochlorothiazide attained a diastolic blood pressure of less than 90 mmHg while less patients required doubling of dosage compared to timolol and enalapril."( The efficacy of hydrochlorothiazide, timolol and enalapril in Ethiopians with essential hypertension.
Habte, B, 1992
)
0.96
"Spontaneous motor activity was measured in six baboons during chronic oral dosing with a diuretic (hydrochlorothiazide/triamterene), a calcium channel blocker (verapamil), and a combination of the two drugs."( Chronic hydrochlorothiazide and verapamil effects on motor activity in hypertensive baboons.
Allen, RP; Hienz, RD; Turkkan, JS, 1992
)
0.93
" L/HCTZ appears to be a well-tolerated combination with efficacy on once-daily dosing superior to that of C/HCTZ."( Treating mild-to-moderate hypertension: a comparison of lisinopril-hydrochlorothiazide fixed combination with captopril and hydrochlorothiazide free combination.
Graham, RD, 1991
)
0.52
" Dosing with hydrochlorothiazide alone resulted in a mean peak serum concentration of 53 ng/ml, 2-6 hours post dose."( The pharmacokinetics of co-administered lisinopril and hydrochlorothiazide.
Swaisland, AJ, 1991
)
0.9
" The pharmacokinetic behaviour of lisinopril and hydrochlorothiazide given together to elderly and renally impaired hypertensive patients suggests that a fixed dose combination is appropriate and that no changes to the dosage regimen additional to those used for the individual agents are necessary."( The effects of age and renal impairment on the pharmacokinetics of co-administered lisinopril and hydrochlorothiazide.
Connell, PA; Hosie, J; Laher, MS; Mulkerrins, E; Smith, RP; Swaisland, AJ, 1991
)
0.75
" The patients were treated for 3 months with monthly assessments, "uncontrolled" patients (DBP greater than 90 mm Hg) had their dosage doubled and then, if necessary, atenolol 50 mg was added."( A double-blind comparison of perindopril and hydrochlorothiazide-amiloride in mild to moderate essential hypertension.
Andrejak, M; Carré, A; Deruyttere, M; Gotzen, R; Magometschnigg, D; Santoni, JP; Stumpe, KO, 1991
)
0.54
" During treatment, the investigator was permitted to adjust the dosage of ramipril and HCTZ according to BP response and tolerance."( Efficacy and safety of ramipril in combination with hydrochlorothiazide: results of a long-term study.
Bauer, B; Breitstadt, A; Cairns, V; Froer, KL; Heidbreder, D, 1991
)
0.53
"5 h after dosing with HCTZ, which was not significantly lower."( Comparison of once daily felodipine 10 mg ER and hydrochlorothiazide 25 mg in the treatment of mild to moderate hypertension.
Binner, L; Hehr, R; Hombach, V; Koenig, W; Rosenthal, J; Sund, M, 1991
)
0.54
" Although some patients may be controlled throughout the entire dosing interval when felodipine is administered bid, many patients will require more frequent dosing to obtain adequate BP control."( Felodipine: a new dihydropyridine calcium-channel antagonist.
Lopez, LM; Yedinak, KC, 1991
)
0.28
" For this reason we studied the influence of different dosing times on the antihypertensive effect over 24 h using ambulatory blood pressure monitoring (ABPM)."( Chronopharmacology of captopril plus hydrochlorothiazide in hypertension: morning versus evening dosing.
Holzgreve, H; Klüglich, M; Middeke, M, 1991
)
0.55
" The author suggests that combined therapy with hydrochlorothiazide, vitamin D3 and calcium prevents hypercalciuria but may require changes in vitamin D3 dosage and withdrawal of hydrochlorothiazide in some patients."( [Effect of hydrochlorothiazide on calcium metabolism in postoperative hypoparathyroidism].
Sawicki, A,
)
0.78
" The 20 mg dosage of benazepril lowered blood pressure to a degree equal to that of 25 mg hydrochlorothiazide: -12."( The effects of benazepril, a new angiotensin-converting enzyme inhibitor, in mild to moderate essential hypertension: a multicenter study.
Abraham, PA; Bennett, WM; Brachfeld, N; Goodman, RP; Hollifield, JW; Kirkendall, WM; Lasseter, KC; Leon, AS; McKenney, JM; Moser, M, 1991
)
0.5
"Behavioral performances of six baboons were tested during chronic oral dosing with diuretic (hydrochlorothiazide/triamterene), a calcium channel blocker (verapamil), and a combination of the two drugs."( Behavioral effects of chronic, orally administered diuretic and verapamil in baboons.
Hienz, RD; Turkkan, JS, 1991
)
0.5
" This combination is well tolerated, probably due to an adequate enalapril/HCTZ dosage ratio."( [Comparative study of enalapril, hydrochlorothiazide and their combination in the treatment of essential hypertension].
Delage, Y; Poggi, L; Souchet, T; Vaisse, B, 1991
)
0.56
" We concluded that enalapril in combination with hydrochlorothiazide is more effective and safe, and allows for lower dosing of enalapril than the drug as monotherapy in Korean hypertensives."( Treatment of essential hypertension in Asians: enalapril as monotherapy versus combination therapy with hydrochlorothiazide.
Jones, DW; Sands, CD, 1991
)
0.75
" If necessary, dosage adjustments were performed every 2 weeks."( Clinical aspects of antihypertensive therapy with urapidil. Comparison with hydrochlorothiazide.
Distler, A; Haerlin, R; Hilgenstock, G; Passfall, J, 1990
)
0.51
" In 2-year studies using dietary concentrations of 0, 250, 500 and 2000 ppm in rats and 0, 2500 and 5000 ppm in mice, survival of dosed and control groups of rats and mice was similar, as were body weights of mice."( Toxicology and carcinogenicity studies of diuretics in F344 rats and B6C3F1 mice. 1. Hydrochlorothiazide.
Bucher, JR; Davis, WE; Elwell, MR; Eustis, SL; Haseman, JK; Huff, J; Meierhenry, EF, 1990
)
0.5
"We studied the dose-response relationship for hydrochlorothiazide + triameterene and verapamil, comparing monotherapy with combined treatment in 216 hypertensive patients over 3 weeks of active treatment following a 2-week washout period with placebo."( Dose-response curves in antihypertensive combination therapy: results of a controlled clinical trial.
Bluemner, E; Letzel, H, 1990
)
0.54
" This system is applied to the analysis of dosage forms containing spironolactone in both single-component formulation and in combination with hydrochlorothiazide."( HPLC-photolysis-electrochemical detection in pharmaceutical analysis: application to the determination of spironolactone and hydrochlorothiazide in tablets.
Bachman, WJ; Stewart, JT, 1990
)
0.69
" Venous blood was taken before and 6 and 24 h after dosing and the serum was analysed for the same solutes as urine."( Renal excretory actions of furosemide, of hydrochlorothiazide and of the vasodilator flosequinan in healthy subjects.
Leary, WP; Reyes, AJ; van der Byl, K; Wynne, RD,
)
0.4
" The patients' blood pressure and heart rate were evaluated biweekly and drug dosage was titrated (up to 400 mg and 50 mg bid of labetalol and HCTZ, respectively) to achieve a standing diastolic blood pressure less than 90 mm Hg."( Comparison of labetalol and hydrochlorothiazide in elderly patients with hypertension using 24-hour ambulatory blood pressure monitoring.
Due, DL; Sirgo, MA; Toth, PD; Vidt, DG; Weidler, DJ, 1990
)
0.57
" Diuretic agents allow dosing rate flexibilities because the temporal profile of diuretic action can vary considerably as long as the total diuretic effect per day is the same."( Optimization of the therapeutic index by adjustment of the rate of drug administration or use of drug combinations: exploratory studies of diuretics.
Levy, G; Zhi, J, 1990
)
0.28
" On repeated daily oral dosing to SHR, both compounds had a cumulative antihypertensive effect."( Biological properties of the angiotensin-converting enzyme inhibitor cilazapril.
Brewster, M; Budd, J; Francis, RJ; Klevans, LR; Natoff, IL; Nixon, JS; Patel, AT; Wenger, J; Worth, E,
)
0.13
" After at least 6 months of treatment, the mean daily dosage of indoramin was higher among patients who received indoramin alone (122 mg/day) than among those who received indoramin plus a diuretic (92 mg/day)."( Antihypertensive therapy with indoramin in the elderly.
Allen, IE; Deitch, MW; Pascucci, VL, 1986
)
0.27
"05) leftward shift in the dose-response relationship, that is, a smaller epinephrine concentration produced earlier onset of ventricular arrhythmias and mortality from fatal ventricular arrhythmias."( Effect of chronic diuretics on epinephrine-induced ventricular arrhythmias: a comparison of hydrochlorothiazide and amiloride in the rat.
Rabkin, SW; Roob, O, 1987
)
0.49
" The patients were re-examined monthly and their treatment was modified if their BP was insufficiently controlled (DAP greater than 90 mmHg): first, the dosage of the drug was doubled, then another antihypertensive agent was added, which was either a diuretic (studies with C or A) or a beta-blocker (studies with D)."( [Perindopril: first-line treatment of arterial hypertension].
Desche, P; Zanchetti, A, 1989
)
0.28
" Dosage modifications are unnecessary in renal impairment, but the dosage regimen for patients with hepatic impairment is not yet established."( The safety of amlodipine.
Osterloh, I, 1989
)
0.28
" A very flat dose-response curve in high dosages and the expectation of fewer side effects made us combine low-dose captopril with enhanced stimulation of the renin-angiotensin-aldosterone (RAA) system."( Captopril and hydrochlorothiazide in the fixed combination multicenter trial.
Lederle, RM, 1985
)
0.63
"Nifedipine, in a slow release preparation, was given at a mean daily dosage of 47 +/- 4 mg to 12 patients with severe hypertension in whom arterial pressure was not satisfactorily controlled (mean arterial pressure 132 +/- 4 4 mm Hg) by the combination of a converting enzyme inhibitor and a diuretic."( Effect of chronic nifedipine in patients inadequately controlled by a converting enzyme inhibitor and a diuretic.
Mimran, A; Ribstein, J, 1985
)
0.27
" Its onset and duration of action and the dose-response relationship of its antihypertensive effect have been evaluated."( Definition of the effective dose of the converting-enzyme inhibitor benazepril.
Whalen, JJ, 1989
)
0.28
" Although some patients remained normotensive after discontinuation of step II drugs, a greater proportion returned to elevated BP than when step II dosage was unchanged."( Effects of reduction in drugs or dosage after long-term control of systemic hypertension.
Borreson, RE; Fisher, SG; Freis, ED; Hamburger, R; Mezey, KC; Mukherji, B; Neal, WW; Perry, HM; Taguchi, JT; Thomas, JR, 1989
)
0.28
" Thus hydrochlorothiazide and zofenopril given once daily at low dosage both reduce office and ambulatory blood pressures and are well tolerated."( Comparative effects of zofenopril and hydrochlorothiazide on office and ambulatory blood pressures in mild to moderate essential hypertension.
Lacourcière, Y; Provencher, P, 1989
)
1.03
" Blood pressure control was better after two than after one month on each of the various dosing schedules."( [Comparison of single and double doses of hydrochlorothiazide in the treatment of arterial hypertension with special emphasis on changes in vascular reactivity].
Bagatin, J; Jurisić, M; Polić, S; Rakić, D; Rumboldt, Z,
)
0.4
" As a result of the pharmacokinetic findings caution may be indicated in the clinical dosage of the diuretics particularly when in fixed dose combination."( The pharmacokinetics of amiloride-hydrochlorothiazide combination in the young and elderly.
Ismail, Z; Parke, W; Smithurst, BA; Triggs, EJ, 1989
)
0.56
" Doses of study medications were administered twice daily and were increased at weekly intervals until the average supine diastolic blood pressure was 90 mm Hg or less, with a decrease from baseline of at least 10 mm Hg, or until the maximum specified dosage of a given study drug was reached."( Comparative trials of terazosin with other antihypertensive agents.
Ruoff, G, 1986
)
0.27
" Once blood pressure control was established, patients received maintenance therapy at that dosage and were followed for up to 12 months."( The long-term antihypertensive effects of prazosin and atenolol.
Itskovitz, HD; Khoury, S; Krug, K; Mollura, JL, 1989
)
0.28
" In controlled double-blind studies involving approximately 550 patients on doxazosin 1-16 mg once daily, significant reductions in both standing and supine BP were maintained throughout the 24 h dosing interval."( The antihypertensive effects of doxazosin: a clinical overview.
Cox, DA; Leader, JP; Milson, JA; Singleton, W, 1986
)
0.27
" In rats, continuous infusion of ANF resulted in a bell-shaped dose-response relationship."( The character of the atrial natriuretic response: pressure and volume effects.
Blaine, EH; Heinel, LA; Marsh, EA; Schorn, TW; Whinnery, MA, 1986
)
0.27
" The commonest adverse reaction with enalapril was dizziness which occurred in two cases and resolved on dosage reduction."( Enalapril maleate and atenolol combined with hydrochlorothiazide in moderate to severe essential hypertension.
Gray, D; Moon, R; Musgrove, J; Pascoe, J, 1985
)
0.53
" After hydrochlorothiazide was added to patients not achieving 'target' blood pressure, the fall in systolic pressure was significantly greater in the enalapril group than in the atenolol group, despite similar dosage of hydrochlorothiazide in the two groups."( Enalapril in moderate to severe hypertension: a comparison with atenolol.
Burgess, J; Cooper, WD; Davidson, C; Fairhurst, G; Petrie, JC; Richardson, PJ; Robb, OJ; Trafford, J; Vandenburg, MJ; Webster, J, 1986
)
0.73
" There was no evidence of a flat dose-response curve in the daily dose range of 12."( Is low-dose hydrochlorothiazide effective?
Freis, ED; Magee, PF, 1986
)
0.65
"Nifedipine, in a slow release preparation, was given at a mean daily dosage of 47 +/- 4 mg to 12 patients with severe hypertension in whom arterial pressure was not satisfactorily controlled (mean blood pressure, 172 +/- 6/111 +/- 4 mmHg) by the association of a converting enzyme inhibitor and a diuretic."( Effect of nifedipine in hypertension not controlled by converting enzyme inhibitor and diuretic.
Mimran, A; Ribstein, J, 1986
)
0.27
"5 h) captopril dosing were similar to those of HCTZ after acute (6."( Pharmacokinetics and biological effects of captopril and hydrochlorothiazide after acute and chronic administration either alone or in combination in hypertensive patients.
Giudicelli, JF; Mattei, A; Richer, C, 1987
)
0.52
"5mg bid, respectively, with significant attenuation of these effects at both hydrochlorothiazide dosage levels."( Pinacidil with and without hydrochlorothiazide. Dose-response relationships from results of a 4 x 3 factorial design study.
Goldberg, MR; Offen, WW, 1988
)
0.8
"This study describes the principle of a simple rapid method for encapsulating hydrochlorothiazide in butyl half-ester of polyvinyl methyl ether-maleic anhydride copolymer to produce a controlled release dosage form."( Preparation and release kinetics of hydrochlorothiazide from butyl half-ester of PVM/MA microcapsules.
el Egaky, MA; el Khodery, K; Mortada, SA; Motawi, AM,
)
0.63
" After the increase in dosage blood pressure was lowered further."( Felodipine versus Moduretic. A double-blind parallel-group multicentre study.
Flygt, G; Krönig, B, 1987
)
0.27
" Patients either remained on this regimen for a further 8 weeks or, if their blood pressure was not controlled, dosage was increased to 2 tablets daily."( An open study to compare the efficacy and tolerability of two diuretic combinations, frusemide plus amiloride and hydrochlorothiazide plus amiloride, in patients with mild to moderate essential hypertension.
Allman, S; Backhouse, CI; Crawford, RJ; Platt, J, 1988
)
0.49
" Dosage was doubled at week 8 in non-responders."( Diltiazem compared with hydrochlorothiazide in the treatment of mild-to-moderate essential hypertension.
Leary, WP; van der Byl, K, 1988
)
0.58
" Eumagnesaemia and eupotassaemia were preserved at all dosage of the piretanide monosubstance."( Lack of effect of piretanide (a potassium-stable diuretic) on serum magnesium.
de Looze, S; Irmisch, R; Rangoonwala, B; Verho, M, 1987
)
0.27
"After a run-in period of 8 weeks on a regimen of hydrochlorothiazide (HCT, median dosage 75 mg/day), patients with essential hypertension were randomly allocated to continued hydrochlorothiazide therapy (Group I) or additional treatment with amiloride (Group II, median dosage 15 mg/day, or 5 mg per 25 mg hydrochlorothiazide) for the following 12 weeks."( Effects of combined therapy with amiloride and hydrochlorothiazide on plasma and total body potassium, blood pressure, and the renin-angiotensin-aldosterone system in hypertensive patients.
Dige-Petersen, H; Giese, J; Ibsen, H; Leth, A; Nielsen, MD; Rasmussen, S; Svendsen, UG, 1986
)
0.78
" The side effects produced were only mild in nature and did not require any change in dosage schedule."( Low-dose captopril alone and in combination with hydrochlorothiazide in the treatment of mild to moderate essential hypertension.
Mondal, S; Pandhi, P; Sharma, BK; Sharma, PL; Wahi, PL, 1986
)
0.53
" Previous medication was stopped and following a run-in period of 2 weeks on placebo, the initial dosage was C (25 mg)/HCT (12."( Captopril/hydrochlorothiazide combination in elderly patients with mild-moderate hypertension. A double-blind, randomized, placebo-controlled study.
Baulac, L; Creisson, C; Lenfant, B, 1986
)
0.67
" After 4 weeks the captopril dosage was doubled, whereas the hydrochlorothiazide dose remained at 25 mg for an additional 4 weeks."( Once-daily treatment of essential hypertension with captopril.
Schoenberger, JA; Wilson, DJ, 1986
)
0.51
"A multicentre controlled trial was carried out to determine the optimal dosage of a 2/1 combination of captopril plus hydrochlorothiazide (HCTZ) in mild hypertension at three doses against placebo in a 6 week double-blind trial."( Determination of the optimal dosage regimen of captopril + hydrochlorothiazide in the treatment of moderate arterial hypertension.
Childs, M; Lancrenon, S; Languillat, JM; Mattei, A; Millet, B; Schwebig, A; Stephan, A; Steru, D, 1987
)
0.73
" Furthermore, no adverse effects were noted with either potassium chloride formulation, and patient acceptance, tolerability, and compliance to prescribed dosing regimens were similar for both products."( Therapeutic assessment of Slow-K and K-tab potassium chloride formulations in hypertensive patients treated with thiazide diuretics.
Acchiardo, SR; Carter, CA; Skoutakis, VA, 1987
)
0.27
" In the dosage used, amiloride did not have a zinc-sparing effect."( Hydrochlorothiazide-amiloride causes excessive urinary zinc excretion.
Averbukh, Z; Cohen, N; Golik, A; Modai, D; Shaked, U; Sigler, E; Weissgarten, J; Zaidenstein, R, 1987
)
1.72
" Both nisoldipine and the diuretic had a flat dose-response curve."( Monotherapy with the calcium channel antagonist nisoldipine for systemic hypertension and comparison with diuretic drugs.
Daniels, AR; Opie, LH, 1987
)
0.27
" A therapeutically satisfactory result has been reached with the administered dosage of both Canrenon and the comparison group."( [Studies on the bioequivalence of canrenone using pharmacokinetic data and clinical effects].
Gopold, B; Schneider, J; Wallnöfer, H, 1987
)
0.27
" The procedure is shown applicable to the analysis of a combination dosage form and is also useful for either drug in a single component dosage form."( Liquid chromatographic determination of guanethidine salts and hydrochlorothiazide using electrochemical detection and ion-pair techniques.
Clark, SS; Stewart, JT, 1986
)
0.51
"In this study we compared the absorption and disposition of two commonly used combination formulations of hydrochlorothiazide and triamterene (Dyazide and Maxzide) in 48 patients with essential hypertension after dosing with each formulation to steady state."( Absorption and disposition of two combination formulations of hydrochlorothiazide and triamterene: influence of age and renal function.
Benet, LZ; Blume, C; Clark, TS; Lin, E; Thornhill, MD; Upton, RA; Williams, RL, 1986
)
0.73
" The effects of increases of calcitriol dosage and modifications of calciuria with hydrochlorothiazide were systematically examined."( Hypercalciuria associated with long-term administration of calcitriol (1,25-dihydroxyvitamin D3). Action of hydrochlorothiazide.
Chan, JC; Santos, F; Smith, MJ, 1986
)
0.71
", following the initial dose of active treatment) and on each visit when the dosage was increased."( The effects of treatments with labetalol and hydrochlorothiazide on ventilatory function of asthmatic hypertensive patients with demonstrated bronchosensitivity to propranolol.
Blasucci, DJ; Falliers, CJ; Maloy, JW; Medakovic, M; Vrchota, J, 1985
)
0.53
" Each dosage of hydrochlorothiazide was given for four weeks, with a two-week placebo washout period intervening."( Antihypertensive efficacy of two low dosages of hydrochlorothiazide in patients treated with captopril.
Ambrosioni, E; Borghi, C; Costa, FV; Mussi, A, 1985
)
0.87
"Ten healthy adult men participated in a study to evaluate appropriate dosing schedules of cholestyramine to minimize its effect on the absorption of hydrochlorothiazide (HCTZ)."( Influence of time intervals for cholestyramine dosing on the absorption of hydrochlorothiazide.
Hibbard, DM; Hunninghake, DB, 1986
)
0.7
"The efficacy and safety of low-dose guanadrel sulfate were evaluated in 20 patients with essential hypertension based on seated diastolic blood pressures (SDBP) ranging from 95 to 115 mm Hg despite a trial dosage of hydrochlorothiazide 50 mg/d for up to five weeks."( A dose-titration trial of guanadrel as step-two therapy in essential hypertension.
Ferguson, RK; Koplin, JR; Latini, V; Oren, A; Riley, LJ; Rotmensch, HH; Vlasses, PH,
)
0.32
"The efficacy of hydrochlorothiazide, in a usual dosage of 50 mg."( The use of thiazides in the prevention of renal calculi.
Garcia, DA; Guay, GF; Yendt, ER, 1970
)
0.59
"001); however, this was not observed until after 4 weeks of treatment when the dosage was 30 and 150 mg X kg-1 X day-1, respectively."( Systolic blood pressure responses to enalapril maleate (MK 421, an angiotensin converting enzyme inhibitor) and hydrochlorothiazide in conscious Dahl salt-sensitive and salt-resistant rats.
Fernandez, PG; Kim, BK; Sharma, JN; Triggle, CR, 1984
)
0.48
" In a randomized, double-blind study, 29 subjects (28 blacks and one white) received one of the following dosing regimens: hydrochlorothiazide (HCTZ), 25 mg twice a day (group 1; n = 12); enalapril, 10 mg twice a day (group 2; n = 12); or enalapril, 10 mg twice a day, with HCTZ, 25 mg twice a day (group 3; n = 5)."( Blood pressure, plasma volume, and catecholamine levels during enalapril therapy in blacks with hypertension.
Bain, RP; Douglas, MB; Freier, PA; Hall, WD; Unger, DJ; Wollam, GL, 1984
)
0.47
" Both acutely and chronically in patients with essential hypertension, enalapril reduced blood pressure with a rather flat dose-response curve."( An overview of the clinical pharmacology of enalapril.
Davies, RO; Gomez, HJ; Irvin, JD; Walker, JF, 1984
)
0.27
" Thus even in low dosage sotalol may be hazardous in the presence of hypokalaemia or when combined with drugs that also prolong the QT interval."( Sotalol, hypokalaemia, syncope, and torsade de pointes.
Barlow, JB; McKibbin, JK; Millar, RN; Obel, IW; Pocock, WA, 1984
)
0.27
"In spontaneously hypertensive rats (SHR), after 1 day of dosing with an angiotensin-converting enzyme (ACE) inhibitor (captopril or enalapril) plus a diuretic (hydrochlorothiazide), a synergistic antihypertensive effect was observed when a second dose of the combination or ACE inhibitor alone but not the diuretic alone was given the next day."( Acute antihypertensive synergism of angiotensin-converting enzyme inhibitors and diuretics.
Cervoni, P; Chan, PS; Ronsberg, MA, 1984
)
0.46
" The reduction in blood pressure following enalapril was evident throughout the 12-hour dosing interval."( Comparative antihypertensive effects of enalapril maleate and hydrochlorothiazide, alone and in combination.
Ferguson, RK; Irvin, JD; Koplin, JR; Lee, RB; Rotmensch, HH; Swanson, BN; Vlasses, PH,
)
0.37
" Dosages were titrated until the patient showed a sitting diastolic blood pressure less than or equal to 90 mm Hg or to a maximum dosage of 100 mg/day of hydrochlorothiazide, 320 mg of propranolol and 20 mg of prazosin."( Monotherapy in mild to moderate hypertension: comparison of hydrochlorothiazide, propranolol and prazosin.
Benowitz, N; Inouye, I; Loge, D; Massie, B; Simpson, P; Topic, N, 1984
)
0.71
" Apart from the hydrochlorothiazide dosage which was fixed, the dosage of the other active drugs was titrated incrementally until the target blood pressure level was achieved."( An appraisal of antihypertensive efficacy and adverse reactions with two drug regimens: enalapril maleate as part of triple therapy compared to conventional triple therapy in moderate to severe hypertension.
Fernandez, PG; Galway, AB; Kim, BK, 1984
)
0.61
" Combination of HCTZ with captopril reduced average standing blood pressure to 111/76 mm Hg at 3 months and 116/81 mm Hg at 1 year while allowing reductions in average captopril dosage to 100 mg/day and HCTZ dosage to 40 mg/day and reductions in supplemental potassium administration and in HCTZ-induced hyperglycemia."( Synergistic effect of captopril with hydrochlorothiazide for the treatment of low-renin hypertensive black patients.
Anderson, RJ; Campbell, WB; Holland, OB; von Kuhnert, L,
)
0.4
" Full PH dose-response curves for standard antihypertensive drugs were explored and were compared to their hypotensive dose-response curves."( Antihypertensive drugs: their postural hypotensive effect and their blood pressure lowering activity in conscious normotensive rats.
Carver, LA; Lee, CH; Strosberg, AM, 1983
)
0.27
" Indoramin dosage was subsequently adjusted in 25 mg steps (to maximum 150 mg daily), if necessary, at follow-up control visits every 14 days."( Indoramin as second step therapy in the management of benign essential hypertension.
Gherardi, S; Manzoli, U; Mazzari, M; Montenero, AS; Schiavoni, G, 1983
)
0.27
" All study designs but 1 called for dosage to be increased to a maximum of 480 mg/day."( Clinical responses to oxprenolol in the elderly.
Ellis, RA, 1983
)
0.27
"We measured the first dosage effect and the long-term effect of lofexidine on blood pressure, heart rate, plasma catecholamines, and their major metabolites in 16 patients with primary hypertension who were receiving 50 mg hydrochlorothiazide twice a day while they were recumbent and upright and during isometric handgrip contraction."( Hemodynamic effect of lofexidine with a diuretic in hypertension.
Alexander, N; Maronde, RF; Velasquez, M; Vlachakis, ND, 1983
)
0.45
" It is therefore concluded that the relationship between the serum chlorthalidone level and the fall in serum potassium level is in keeping with the flat dose-response curves for the thiazide and phthalimide diuretics."( The effects of two combinations of a beta-blocker and a diuretic on diuresis in normal subjects.
Schoeman, HS; Sommers, DK; van Wyk, M, 1984
)
0.27
" We feel that in developing countries, where the cost of therapy is important, reserpine in a dosage of less than 0,1 mg/d plus a thiazide derivative in low dosage is preferable to a beta-blocker plus a thiazide derivative in the treatment of hypertension."( Reserpine plus hydrochlorothiazide and sotalol plus hydrochlorothiazide in Black and Indian hypertensive patients.
Bhigjee, AI; Hoosen, S; Seedat, YK, 1984
)
0.62
"Twenty patients with mild to moderate hypertension participated in a single-blind crossover comparison of treatment with 25 mg hydrochlorothiazide plus 50 mg triamterene and 50 mg hydrochlorothiazide plus 5 mg amiloride in once-daily dosage regimens."( Hydrochlorothiazide in combination with potassium-sparing agents in the treatment of hypertension.
Dean, S; Spencer-Mills, L, 1984
)
1.92
" The dosage range that is likely to cause the hypotensive effect without the potassium loss has been called the "therapeutic window."( Effect of bioavailability on dose-response relationships.
Goldman, P, 1984
)
0.27
" Compound 9d, which lowered arterial blood pressure 37 mmHg in SHR when dosed at 100 mg/kg, was further evaluated in chronic hypertensive dogs because of apparent minimal CNS effects."( N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as antihypertensive and diuretic agents.
Chan, PS; Emma, JE; Meyer, WE; Tomcufcik, AS, 1984
)
0.27
"An open, multi-centre study was carried out in general practice to compare the efficacy and tolerance of antihypertensive therapy with once-daily and twice-daily dosage of a fixed ratio combination of hydrochlorothiazide (25 mg), amiloride (2."( Comparison of a fixed ratio combination of hydrochlorothiazide, amiloride and timolol ('Moducren') given once versus twice daily in mild to moderate hypertension.
Currie, WJ; Isitt, VL; VandenBurg, MJ; Young, JH, 1984
)
0.72
" There were no significant differences among the three dosage levels of indapamide."( Indapamide, a new antihypertensive/diuretic agent, in the treatment of patients with edema.
Bratnick, J; Eff, J; Neiss, E; Vukovich, RA; Zisblatt, M, 1984
)
0.27
" Very slight accumulation of sotalol and hydrochlorothiazide was observed, so it appears unnecessary to reduce the dosage in patients with a creatinine clearance of 30 ml/min or more."( Pharmacokinetics of a fixed combination of sotalol and hydrochlorothiazide in hypertensive patients with moderate renal insufficiency.
Fillastre, JP; Fourtillan, JB; Ingrand, I; Kher, A; Lefebvre, MA, 1984
)
0.78
" A well-formulated hydrochlorothiazide-triamterene combination tablet promotes plasma concentrations and urinary excretion of hydrochlorothiazide, triamterene, and hydroxytriamterene sulfate which are virtually identical to those seen after either a combination liquid dosage form or simple liquid forms containing only one of the two drugs."( Absence of a significant pharmacokinetic interaction between hydrochlorothiazide and triamterene when coadministered.
Benet, LZ; Blume, CD; Gee, WL; Lin, ET; Upton, RA; Williams, RL, 1984
)
0.84
"Total body potassium content, plasma potassium concentration, blood pressure, and plasma concentrations of renin, angiotensin II, and aldosterone were measured in patients with essential hypertension after a run-in period of 8 wk on a regimen of hydrochlorothiazide (median dosage 75 mg/day)."( Effects of amiloride on plasma and total body potassium, blood pressure, and the renin-angiotensin-aldosterone system in thiazide-treated hypertensive patients.
Dige-Petersen, H; Giese, J; Ibsen, H; Leth, A; Nielsen, MD; Rasmussen, S; Svendsen, UG, 1983
)
0.45
" All groups had mean diastolic pressure controlled at or below the 90 mmHg criterion during the period of constant methyldopa dosage for those patients who required Step 2 therapy."( Indapamide in the stepped-care treatment of obese hypertensive patients.
Godfrey, JC; Neiss, ES; Noble, RE; Vukovich, RA; Webb, EL; Zisblatt, M, 1983
)
0.27
" Recoveries from commercial dosage forms ranged from 99."( Liquid chromatographic determination of methyldopa and methyldopa-thiazide combinations in dosage forms.
Ting, S, 1983
)
0.27
" They had simultaneously started therapy with, or increased the dosage of, chlorthalidone or hydrochlorothiazide for the treatment of hypertension."( Serum cholesterol during treatment of hypertension with diuretic drugs.
Ames, RP; Peacock, PB, 1984
)
0.49
" No differences between the dose-response curves of furosemide, bumetanide, or piretanide could be demonstrated."( Effect of diuretics on the tubuloglomerular feedback response.
Brunkhorst, R; Franke, H; Gutsche, HU; Müller-Ott, K; Niedermayer, W, 1984
)
0.27
" The effect of twice the dosage was evaluated in subjects with unsatisfactory blood pressure (BP) on the lower dose."( Potassium sparing by amiloride during thiazide therapy in hypertension.
Andersson, PO; H-Andersen, H; Hagman, A; Henning, R, 1984
)
0.27
" Also during treatment, fewer patients receiving hydrochlorothiazide required termination as compared with those receiving propranolol; comparative dosage requirements were lower; additional titration during long-term treatment was required less often, and BP remained lower after withdrawal of the active drugs."( Comparison of propranolol and hydrochlorothiazide for the initial treatment of hypertension. II. Results of long-term therapy. Veterans Administration Cooperative Study Group on Antihypertensive Agents.
, 1982
)
0.81
" It remained essentially unchanged for the duration of the 2-year study, and no increases in the dosage of either drug were needed."( Long-term treatment of essential hypertension with Nadolol and Hydrochlorothiazide: a two-year follow-up.
El-Mehairy, MM; Hamza, S; Ramadan, M; Shaker, A; Tadros, SS, 1982
)
0.5
" The results showed that the change in treatment led to a significant reduction in blood pressure in both groups, at a dosage of 1 tablet daily in over half the patients, and the majority (88%) preferred the new form of treatment."( A general practice study of timolol/hydrochlorothiazide/amiloride ('Moducren'), a new therapy for hypertension, and the doctor's influence on management.
Arr, S; Parry, EE; Tait, D, 1983
)
0.54
" In patients with an endogenous creatinine clearance of 30 to 90 ml/min, the dosage of HCT should be reduced to 1/2 and in patients with a endogenous creatinine clearance below 30 ml/min to 1/4 of the normal daily dose to avoid dose dependant side-effects."( Pharmacokinetics of hydrochlorothiazide in relation to renal function.
Hasenfuss, G; Knauf, H; Mutschler, E; Niemeyer, C; Schäfer-Korting, M; Wais, U, 1983
)
0.59
" In terms of lofexidine, there was no evidence of any adverse interactions with hydrochlorothiazide either following a single, oral administration to rats and mice or following short-term and long-term repeated oral dosing of rats and dogs."( Toxicology of the combination lofexidine/hydrochlorothiazide.
Fontaine, R; Friehe, H; Gibson, JP; Larson, EJ; Sells, DM, 1982
)
0.76
" The dosage of guanabenz was adjusted upward from 16 mg/day until blood pressure normalized or side effects intervened."( Preliminary clinical trial with a new hypotensive, guanabenz, in a group of hypertensive patients.
De Ridder, JH; Marchandise, P, 1980
)
0.26
" Treatment with guanabenz plus hydrochlorothiazide proved more satisfactory than treatment with guanabenz plus placebo in that fewer patients were treatment failures, a smaller dosage of guanabenz was required, better control of supine blood pressure was achieved, and no increase in guanabenz dosage was needed to maintain chronic blood pressure control."( Effect of guanabenz and hydrochlorothiazide on blood pressure and plasma renin activity.
Fairchild, C; Gomez-Sanchez, CE; Holland, OB, 1981
)
0.86
" The dosage problem with HTZ + AMl is discussed."( Antihypertensive and metabolic effects of a combination of hydrochlorothiazide and amiloride.
Leary, WP; Reyes, AJ, 1981
)
0.51
" A significant dose-response curve between the dose of captopril (range 75 to 450 mg/day) and the antihypertensive effect was obtained with a maximum at 300 mg/day."( [Effect of captopril in essential hypertension (author's transl)].
Laroche, B; Mimran, A; Targhetta, R, 1981
)
0.26
"1 The hypotensive effect of single daily dosing with 80 mg penbutolol was compared to 100 mg hydrochlorothiazide and placebo in a double-blind cross-over controlled trial with daily home measurements in ten hypertensive patients."( Penbutolol or hydrochlorothiazide once a day in hypertension. A controlled study with home measurements.
De Plaen, JF; Van Ypersele de Strihou, C; Vander Elst, E, 1981
)
0.84
" Dosage was 2 tablets per day of the 5 mg amiloride plus 50 mg hydrochlorothiazide combination or of 50 mg hydrochlorothiazide alone."( Potassium conservation with amiloride/hydrochlorothiazide ("Moduret') in thiazide-induced hypokalaemia in hypertension.
Campbell, N; Fernandez, PG; Galway, AB; Gill, V; Granter-Button, S; Kim, BK; MacDonald, J; Sharma, JN; Snedden, W, 1982
)
0.77
" Further increases in acebutolol dosage to a maximum of 2000 mg daily in 13 patients whose hypertension was not well controlled on lower doses resulted in a mean supine blood pressure of 132/92 mmHg."( Antihypertensive action of acebutolol (Sectral) when used concomitantly with hydrochlorothiazide.
Brossard, JJ; McKenzie, JK; Mitenko, PA, 1982
)
0.49
" The adsorption and disposition of hydrochlorothiazide demonstrate that this drug is rapidly absorbed and produces a diuretic and natriuretic response that peaks at approximately 2 hours after dosing and is essentially terminated 12 hours after dosing."( Hydrochlorothiazide pharmacokinetics and pharmacologic effect: the influence of indomethacin.
Benet, LZ; Berman, RS; Davies, RO; Gee, WL; Holmes, GI; Huber, P; Lin, ET; Williams, RL, 1982
)
1.98
"Experiments have been carried out in dogs and man to determine the effect of hydrochlorothiazide (HCT) on the pharmacokinetics of propranolol and to evaluate the bioavailability of two dosage forms containing both propranolol and HCT (40/25 and 80/25 mg, respectively)."( Biopharmaceutical characteristics of a new propranolol/hydrochlorothiazide tablet combination.
Dubuc, J; Dvornik, D; Kraml, M; Lee, TY; Mullane, J; Patterson-Kreuscher, S; Perdue, H,
)
0.61
"Criteria for the choice of drug dosage are established."( [Determination of the criteria for selecting the optimal obsidan and hypothiazide treatment regimen in hypertension based on mathematical modelling data].
Churnosov, EV; Katiukhin, VN; Temirov, AA, 1981
)
0.26
" Thiazide administration in customary clinical dosage twice a day with substantial sodium chloride and water for the first two days after exposure to 131I, should therefore facilitate the safe excretion of 131I."( Hydrochlorothiazide-induced 131I excretion facilitated by salt and water.
Beyer, KH; Fehr, DM; Gelarden, RT; Lang, CM; Vesell, ES; White, WJ,
)
1.57
" However, a higher proportion of patients achieved satisfactory control (BP less than 160/95 mm Hg) on FUR than on HCT and, in addition, there was a more marked dose-response effect with FUR."( Controlled comparison of the effects of furosemide and hydrochlorothiazide added to propranolol in the treatment of hypertension.
Dombey, SL; Lawrence, J; Vander Elst, E; Vlassak, W, 1981
)
0.51
" The combination of moxonidine and hydrochlorothiazide in the same dosage as a monotherapy improves efficacy significantly without additive effects on the safety profile."( Moxonidine and hydrochlorothiazide in combination: a synergistic antihypertensive effect.
Frei, M; Gardosch von Krosigk, PP; Koch, HF; Küppers, H; Küster, L, 1994
)
0.92
" In this small sample of hypertensive patients, losartan monotherapy and losartan-hydrochlorothiazide (HCTZ) combination therapy were associated with modest reductions in systolic, diastolic and mean arterial BPs; significant changes were observed only at the peak dosing interval."( Effects of losartan on the renin-angiotensin-aldosterone axis in essential hypertension.
Bauer, IH; Lau-Sieckman, A; Reams, GP; Wu, Z, 1995
)
0.52
" A dose-response relationship to losartan was observed in this patient population."( Effects of losartan on a background of hydrochlorothiazide in patients with hypertension.
Goldberg, AI; Pratt, JH; Soffer, BA; Sweet, CS; Wiens, B; Wright, JT, 1995
)
0.56
"01), although the once-daily dosing of enalapril and the maximum dose of 20 mg might not have been optimal for this agent."( Low-dose drug combination therapy: an alternative first-line approach to hypertension treatment.
Adegbile, IA; Alemayehu, D; Carr, AA; Lefkowitz, MP; Papademetriou, V; Prisant, LM; Weber, MA; Weir, MR, 1995
)
0.29
" Hydrochlorothiazide (10 microM) and cicletanine (10 microM) were weak calcium antagonists shifting the calcium dose-response curve half a log unit to the right."( Ion channel involvement in the acute vascular effects of thiazide diuretics and related compounds.
Calder, JA; Schachter, M; Sever, PS, 1993
)
1.2
" Antihypertensive effects were maintained during the 24-hour dosing interval."( First-line therapy option with low-dose bisoprolol fumarate and low-dose hydrochlorothiazide in patients with stage I and stage II systemic hypertension.
Alemayehu, D; Bryzinski, BS; Burris, JF; Chen, SY; Frishman, WH; Mroczek, WJ; Simon, JS; Weir, MR, 1995
)
0.52
" At the end of both periods, sphygmomanometric blood pressure was assessed 24 hours after dosing and 24-hour ambulatory blood pressure was performed, taking blood pressure readings every 15 minutes during day- and night-time."( [The antihypertensive effects of the lisinopril-hydrochlorothiazide combination (Zestoretic) in elderly hypertensive patients. The results of a multicenter study. The Italian Zestoretic Study Group].
Mancia, G, 1994
)
0.54
" It allows instant evaluation of a patient's dosing record, at the patient's return to the practice."( Patterns of drug compliance with medications to be taken once and twice daily assessed by continuous electronic monitoring in primary care.
Kruse, W; Rampmaier, J; Ullrich, G; Weber, E, 1994
)
0.29
"75, 10, and 30 mg) of cilazapril reduced diastolic blood pressure dose-dependently and shifted the angiotensin I dose-response curves to the right."( Review of studies on the clinical pharmacodynamics of cilazapril.
Belz, GG; Breithaupt, K; Erb, K, 1994
)
0.29
"Thiazide diuretics are widely used in the drug treatment of hypertension but their dose-response curves for the antihypertensive and adverse metabolic effects differ."( Relation between low dose of hydrochlorothiazide, antihypertensive effect and adverse effects.
Borrild, NJ; Hoyem, A; Jounela, AJ; Lilja, M; Lumme, J; Mörlin, C; Wessel-Aas, T, 1994
)
0.58
" After 3 months the drug dosage was doubled if the systolic blood pressure goal (SBP < 160 mmHg and SBP reduction of at least 20 mmHg) had not been reached."( Antihypertensive efficacy and tolerability of different drug regimens in isolated systolic hypertension in the elderly.
Alli, C; Avanzini, F; Bettelli, G; Colombo, F; Corso, R; Mariotti, G; Radice, M; Tognoni, G; Torri, V, 1994
)
0.29
"A factorial design method was applied in this multicentre trial of the angiotensin-converting enzyme inhibitor quinapril hydrochloride (Accupril) in combination with the diuretic hydrochlorothiazide (HCTZ) to assess the additive effects of the combination versus monotherapy, to characterise the dose-response relationship of each drug in the presence of the other and to determine if quinapril would attenuate the hypokalemic effect of HCTZ."( Quinapril and hydrochlorothiazide combination for control of hypertension: assessment by factorial design. Quinapril Investigator Group.
Canter, D; Frank, GJ; Knapp, LE; Phelps, M; Quade, M; Texter, M, 1994
)
0.84
"The effects of bisoprolol and hydrochlorothiazide were additive with respect to reductions in diastolic and systolic blood pressures over the dosage ranges studied."( A multifactorial trial design to assess combination therapy in hypertension. Treatment with bisoprolol and hydrochlorothiazide.
Alemayehu, D; Bryzinski, BS; Coulson, LR; DeQuattro, VL; Dukart, G; Frishman, WH; Goldberg, JD; Koury, K; Mroczek, WJ; Vlachakis, ND, 1994
)
0.79
"The utility of factorial design trials to characterize dose-response relationships and to test the potential interactions between various antihypertensive agents has been demonstrated."( A multifactorial trial design to assess combination therapy in hypertension. Treatment with bisoprolol and hydrochlorothiazide.
Alemayehu, D; Bryzinski, BS; Coulson, LR; DeQuattro, VL; Dukart, G; Frishman, WH; Goldberg, JD; Koury, K; Mroczek, WJ; Vlachakis, ND, 1994
)
0.5
"3 years) of whom 89% (n = 510) received the standard dosage of 1 tablet daily."( [Antihypertensive effectiveness of enalapril and hydrochlorothiazide as a combination drug].
Banyai, M; Pirich, C, 1993
)
0.54
" During a 12-hour in-clinic monitoring period spanning a dosing interval, both the combination and DTZ SR therapies maintained efficacy, whereas the antihypertensive effects of HCTZ dissipated after 8 hours."( A randomized, controlled trial comparing diltiazem, hydrochlorothiazide, and their combination in the therapy of essential hypertension.
Applegate, WB; Cady, WJ; Pool, PE; Sandall, P; Woehler, T,
)
0.38
" If seated DBP was > or = 90 mm Hg at any visit, daily dosage of felodipine was doubled to a maximum of 20 mg."( Antihypertensive effect and tolerability of felodipine extended release (ER) tablets in comparison with felodipine plain tablets (PT) and placebo in hypertensives on a diuretic. Canadian Study Group.
Carruthers, SG; Vint-Reed, C, 1993
)
0.29
" Results of both studies demonstrated that this once-a-day, low-dose option effectively reduced sitting diastolic and systolic blood pressure measured at the end of the 24-hour dosing period."( Low-dose bisoprolol/hydrochlorothiazide: an option in first-line, antihypertensive treatment.
Messerli, FH; Mroczek, W; Zachariah, PK,
)
0.45
" During maintenance, patients not at goal were "stepped up," and patients with uncontrolled DBP at maximum dosage were removed from the study."( Efficacy and safety of atenolol, enalapril, and isradipine in elderly hypertensive women.
Bartels, DW; Benz, JR; Due, DL; Hall, WD; Kostis, JB; Peng, A; Perry, HM; Sirgo, M; Townsend, RR, 1994
)
0.29
" Symptom frequency differed little among the three dosage levels, becoming maximal by the second visit at the same dosage level."( Efficacy and safety of atenolol, enalapril, and isradipine in elderly hypertensive women.
Bartels, DW; Benz, JR; Due, DL; Hall, WD; Kostis, JB; Peng, A; Perry, HM; Sirgo, M; Townsend, RR, 1994
)
0.29
" Response surface analyses were performed, and a stairstep model was constructed to characterize the shape of the dose-response surface."( Short report: ramipril and hydrochlorothiazide combination therapy in hypertension: a clinical trial of factorial design. The East Germany Collaborative Trial Group.
Bauer, B; Bender, N; Breitstadt, A; Cairns, V; Koch, G; Moreadith, C; Phillips, J; Priestley, C; Scholze, J; Vander Elst, E, 1993
)
0.58
"Several dosage combinations of ramipril plus HCT produced significantly greater blood pressure reductions than the monotherapies at the same dosages."( Short report: ramipril and hydrochlorothiazide combination therapy in hypertension: a clinical trial of factorial design. The East Germany Collaborative Trial Group.
Bauer, B; Bender, N; Breitstadt, A; Cairns, V; Koch, G; Moreadith, C; Phillips, J; Priestley, C; Scholze, J; Vander Elst, E, 1993
)
0.58
" On the fourth day of once-daily dosing with hydrochlorothiazide 25 mg, 24-hour natriuresis and chloriuresis are no longer augmented, but the elevation in 24-hour kaliuresis that follows the first dose remains unchanged."( Renal excretory responses to single and repeated administration of diuretics in healthy subjects: clinical connotations.
Leary, WP; Reyes, AJ, 1993
)
0.55
" One capsule was taken for three days and then the dosage was doubled for the remainder of a four-week period."( Effect of hydrochlorothiazide, enalapril, and propranolol on quality of life and cognitive and motor function in hypertensive patients.
Annett, MP; Culbert, JP; McCorvey, E; McKenney, JM; Proctor, JD; Wright, JT, 1993
)
0.69
" for K-Can: dosing was doubled after 1 month if seated diastolic BP was > or = 95 mmHg."( Different sensitivity to hydrochlorothiazide and to potassium-canrenoate among essential hypertensive patients.
Cusi, D; Glorioso, N; Madeddu, P; Manunta, P; Melis, MG; Pala, F; Pazzola, A; Soro, A; Tonolo, G; Troffa, C, 1993
)
0.59
" Although plasma inactive renin concentrations did not change acutely after losartan dosing on day 1 or 42 they did increase from 27."( Effect of acute and chronic losartan therapy on active and inactive renin and active renin glycoforms.
Goldberg, MR; Katz, SA; Opsahl, JA, 1995
)
0.29
" After this period, patients with DBP > 90 mmHg had the dosage duplicated, while the others had the same dosage for 60 days more."( [Efficacy and tolerability of the captopril and hydrochlorothiazide combination in the treatment of mild to moderate hypertension. Multicenter study].
Franco, RJ; Martin, LC; Velasco-Cornejo, IF, 1995
)
0.55
" A total of 179 patients with a pretreatment mean baseline BP of 172 +/- 17/112 +/- 18 mm Hg enrolled in the trial and BP was recorded 24 h after dosing at baseline and weeks 2, 4, 8 and the final week (10-12 weeks)."( Losartan potassium as initial therapy in patients with severe hypertension.
Chrysant, S; Dunlay, MC; Fitzpatrick, V; Francischetti, EA; Goldberg, AI; Sweet, CS, 1995
)
0.29
" The dose-response curves for HCTZ and FU were both relatively flat: doubling the dose of each produced statistically insignificant increases in sodium excretion."( Diuretic effectiveness of hydrochlorothiazide and furosemide alone and in combination in chronic renal failure.
Knauf, H; Mutschler, E, 1995
)
0.59
"To discover whether in hypertensives with left ventricular hypertrophy (LVH) the increased muscle mass will completely regress under antihypertensive treatment and drug dosage can in consequence be reduced."( [Decreasing the antihypertensive dosage during longterm treatment and complete regression of left ventricular hypertrophy].
Behr, U; Franz, IW; Ketelhut, R; Tönnesmann, U, 1996
)
0.29
" The drug dosage could either be reduced or the drug completely discontinued in 11 patients (group 1): after 102 +/- 5 months four patients took no drug, while seven were on 100 mg metoprolol."( [Decreasing the antihypertensive dosage during longterm treatment and complete regression of left ventricular hypertrophy].
Behr, U; Franz, IW; Ketelhut, R; Tönnesmann, U, 1996
)
0.29
" In half of them the drug dosage can be reduced or the drug even discontinued."( [Decreasing the antihypertensive dosage during longterm treatment and complete regression of left ventricular hypertrophy].
Behr, U; Franz, IW; Ketelhut, R; Tönnesmann, U, 1996
)
0.29
" We conclude that although the pharmacokinetics of both enalaprilat and HCTZ are related to renal function, HCTZ has no significant effect on the pharmacokinetics of enalaprilat and that dosage adjustment for both regimens should be based on renal function."( Effect of hydrochlorothiazide on the pharmacokinetics of enalapril in hypertensive patients with varying renal function.
Carmody, M; Doyle, GD; Hersh, AD; Kelly, JG; Laher, MS, 1996
)
0.7
" The dosage of cation exchange resins was decreased, oral fluids were tolerated, and the patient's general condition improved."( Effect of hydrochlorothiazide in pseudohypoaldosteronism with hypercalciuria and severe hyperkalemia.
Rosa, FC; Stone, RC; Vale, P, 1996
)
0.7
" The dosage was increased in three patients who had not attained target blood pressure (BP) control after 6 weeks."( Double-blind, parallel, comparative multicentre study of a new combination of diltiazem and hydrochlorothiazide with individual components in patients with mild or moderate hypertension.
Joy, A; Manning, G; Mathias, CJ; McDonald, CJ; Millar-Craig, MW, 1996
)
0.51
" BP control throughout the 24 h dosing interval was demonstrated by ambulatory BP monitoring."( Double-blind, parallel, comparative multicentre study of a new combination of diltiazem and hydrochlorothiazide with individual components in patients with mild or moderate hypertension.
Joy, A; Manning, G; Mathias, CJ; McDonald, CJ; Millar-Craig, MW, 1996
)
0.51
"The stability of drugs commonly prescribed for use in oral liquid dosage forms but not commercially available as such was studied."( Stability of labetalol hydrochloride, metoprolol tartrate, verapamil hydrochloride, and spironolactone with hydrochlorothiazide in extemporaneously compounded oral liquids.
Allen, LV; Erickson, MA, 1996
)
0.51
" Losartan has a sustained duration of action, permitting once-daily dosing in many patients, and lacks partial agonist activity."( The angiotensin II type 1 receptor blocker losartan in clinical practice: a review.
Gavras, HP; Salerno, CM,
)
0.13
"Antihypertensive drug combinations have two major advantages: First, dosage of the single components can be reduced, and second, putative side effects can be minimized."( [Combination antihypertensive therapy in patients with an increased risk profile].
Bartens, W; Nauck, M; Wanner, C, 1996
)
0.29
" This caused regular fall of blood pressure (BP) and development of a flat dose-response curve-both events resembling corresponding phenomena in systemic injections."( Blood pressure effects of hydrochlorothiazide, applied to the rat hypothalamus.
Altshuler, R; Bergmann, F, 1996
)
0.59
" Significant dose-response differences were observed between treatments."( Lisinopril versus hydrochlorothiazide in obese hypertensive patients: a multicenter placebo-controlled trial. Treatment in Obese Patients With Hypertension (TROPHY) Study Group.
Anzalone, DA; Falkner, B; Hutchinson, HG; Reisin, E; Tuck, ML; Weir, MR, 1997
)
0.63
"To evaluate the antihypertensive efficacy, tolerability, safety, and dose-response characteristics of the novel calcium antagonist, mibefradil, in combination with a diuretic regimen."( The addition of mibefradil to chronic hydrochlorothiazide therapy in hypertensive patients is associated with a significant antihypertensive effect.
Carney, S; Kallwellis, R; Kobrin, I; Mion, D; Ribeiro, A; Viskoper, RJ; Wing, L; Zimlichman, R, 1997
)
0.57
"5 mg combination is more effective during the last period of the dosing interval."( [Comparison of antihypertensive and metabolic effects of lisinopril 20 mg/hydrochlorothiazide 12.5 mg fixed combination and captopril 50 mg/hydrochlorothiazide 25 mg fixed combination].
Baleydier, A; Milon, H,
)
0.36
" The cardinal questions to be answered were: (1) the relationship between three targeted diastolic pressures (< or = 90, < or = 85 and < or = 80 mm Hg, respectively) and cardiovascular morbidity and mortality rates among hypertensives; and (2) the effect of low dosage aspirin (75 mg daily) on morbidity and mortality rates, compared with a placebo."( [The Hypertension Optimal Treatment (HOT) study: results of 12-month therapy related to age].
Kolloch, RE; Rahn, KH, 1998
)
0.3
" Any necessary changes in dosage (step 4) were made according to a prescribed plan."( [The Hypertension Optimal Treatment (HOT) study: results of 12-month therapy related to age].
Kolloch, RE; Rahn, KH, 1998
)
0.3
" The only activity observed in mice was an inhibition of spontaneous motility after oral dosing with 300 and 1000 mg/kg, respectively."( Preclinical safety studies of the combination moexipril hydrochloride/hydrochlorothiazide.
Friehe, H; Gietl, R; Ney, P, 1998
)
0.53
" After the first 4 weeks, the patients who responded to the initial dosage (a reduction in systolic blood pressure of at least 15 mm Hg) or whose blood pressure was controlled on the dosage (systolic blood pressure < 140 mm Hg) continued to take the low dose."( Felodipine extended release versus conventional diuretic therapy for the treatment of systolic hypertension in elderly patients. The National Trial Group.
McClennen, W; Wilson, T, 1998
)
0.3
" Dose-response curves were repeated after local tetraethylammonium (TEA) administration to determine the role of potassium channel activation and, in patients with the Gitelman syndrome, to determine the role of the thiazide-sensitive Na-Cl cotransporter in the vasodilator effect of hydrochlorothiazide."( Thiazide-induced vasodilation in humans is mediated by potassium channel activation.
Hughes, AD; Pickkers, P; Russel, FG; Smits, P; Thien, T, 1998
)
0.48
" At week 6, the dosage of irbesartan or placebo was doubled for seated diastolic blood pressure > or = 90 mmHg."( The effects of irbesartan added to hydrochlorothiazide for the treatment of hypertension in patients non-responsive to hydrochlorothiazide alone.
Lin, CS; MacNeil, D; Osbakken, M; Rosenstock, J; Rossi, L, 1998
)
0.58
"A 26-week, multicenter, double-blind, parallel-group, dosage titration study."( Efficacy and safety of telmisartan, a selective AT1 receptor antagonist, compared with enalapril in elderly patients with primary hypertension. TEES Study Group.
Hermansson, K; Karlberg, BE; Lins, LE, 1999
)
0.3
" The telmisartan dosage was increased from 20 to 40-80 mg and that of enalapril from 5 to 10-20 mg at 4-week intervals until trough supine diastolic blood pressure was < 90 mmHg."( Efficacy and safety of telmisartan, a selective AT1 receptor antagonist, compared with enalapril in elderly patients with primary hypertension. TEES Study Group.
Hermansson, K; Karlberg, BE; Lins, LE, 1999
)
0.3
" Both regimens provided effective blood pressure lowering over the 24 h dosing interval, as determined by ambulatory blood pressure monitoring."( Efficacy and safety of telmisartan, a selective AT1 receptor antagonist, compared with enalapril in elderly patients with primary hypertension. TEES Study Group.
Hermansson, K; Karlberg, BE; Lins, LE, 1999
)
0.3
"5 or 25 mg/day to valsartan 80 mg/day resulted in a greater blood pressure reduction than increasing the valsartan dosage from 80 to 160 mg/day."( Valsartan/hydrochlorothiazide.
Langtry, HD; McClellan, KJ, 1999
)
0.71
" For drugs with a narrow therapeutic window, indirect estimates of GFR appear to be an unreliable means for calculating correct dosage in the elderly."( Renal handling of drugs in the healthy elderly. Creatinine clearance underestimates renal function and pharmacokinetics remain virtually unchanged.
Bischoff, I; Block, S; Fliser, D; Hanses, A; Joest, M; Mutschler, E; Ritz, E, 1999
)
0.3
" The primary efficacy variable was the mean change from baseline in seated diastolic BP at the end of the dosing period."( Usefulness of moexipril and hydrochlorothiazide in moderately severe essential hypertension.
Koch, B; Stimpel, M; White, WB, 1997
)
0.59
" Dosage could be increased for both telmisartan (40 --> 80 --> 160 mg) and lisinopril (10 --> 20 --> 40 mg) at each of the first 2 monthly visits if DBP control (<90 mm Hg) had not been established."( Comparison of telmisartan with lisinopril in patients with mild-to-moderate hypertension.
Frishman, WH; Guthrie, G; Neutel, JM; Oparil, S; Papademitriou, V, 1999
)
0.3
"The purpose of this study was to assess the safety and antihypertensive dose-response effects of irbesartan and hydrochlorothiazide (HCTZ) in patients with mild-to-moderate hypertension."( Matrix study of irbesartan with hydrochlorothiazide in mild-to-moderate hypertension.
Guthrie, R; Kassler-Taub, K; Kochar, M; Reeves, RA; Triscari, J, 1999
)
0.8
" Non-compartmental pharmacokinetic parameters of fosinoprilat and HCTZ were determined from blood and urine samples obtained over 48 h starting on Day 1 (single dose) and Day 5 (steady state): maximum serum concentration (Cmax ), time to maximum serum concentration (tmax ), area under the serum concentration-time curve during the dosing interval (AUC), cumulative urinary excretion (CUE) and the accumulation index (AI; ratio of AUC-day 5/AUC-day 1)."( Fosinopril/hydrochlorothiazide: single dose and steady-state pharmacokinetics and pharmacodynamics.
Lins, R; Mangold, B; O'Grady, P; Yee, KF, 1999
)
0.69
"A micro-bore liquid chromatographic method was developed for the simultaneous determination of benazepril hydrochloride and hydrochlorothiazide in pharmaceutical dosage forms."( Simultaneous determination of benazepril hydrochloride and hydrochlorothiazide by micro-bore liquid chromatography.
Panderi, IE; Parissi-Poulou, M, 1999
)
0.75
"A second-order derivative spectrophotometric method for the simultaneous determination of benazepril hydrochloride and hydrochlorothiazide in pharmaceutical dosage forms is described."( Simultaneous determination of benazepril hydrochloride and hydrochlorothiazide in tablets by second-order derivative spectrophotometry.
Panderi, IE, 1999
)
0.76
"Three sensitive and accurate methods are presented for the determination of benazepril in its dosage forms."( Spectrophotometric methods for the determination of benazepril hydrochloride in its single and multi-component dosage forms.
Abdine, HH; El-Yazbi, FA; Shaalan, RA, 1999
)
0.3
"Rapid, precise, accurate and specific ratio spectra derivative spectrophotometry and high-performance liquid chromatographic procedures were described for the simultaneous determination of hydrochlorothiazide and amiloride hydrochloride in combined pharmaceutical dosage forms."( Simultaneous determination of hydrochlorothiazide and amiloride hydrochloride by ratio spectra derivative spectrophotometry and high-performance liquid chromatography.
Erk, N; Kartal, M, 1999
)
0.78
" It is considered one of the most important quality control tests performed on pharmaceutical dosage forms, and validation of dissolution methods is an important part of good manufacturing practices (GMP)."( Validation of tablet dissolution method by high-performance liquid chromatography.
Dluzneski, PR; Guo, JH; Harcum, WW; Skinner, GW; Trumbull, DE, 2000
)
0.31
" Blood was collected at intervals over 48 and 84 hours, respectively, at the end of the 7-day dosing period for the determination of plasma telmisartan and hydrochlorothiazide concentrations by high-performance liquid chromatography."( Multiple-dose pharmacokinetics of telmisartan and of hydrochlorothiazide following concurrent administration in healthy subjects.
Dias, VC; Stangier, J; Young, CL, 2000
)
0.75
"The study was undertaken to assess the tolerability and antihypertensive dose-response efficacy of telmisartan and HCTZ and their combination in black patients with mild to moderate hypertension (mean supine blood pressure 140/95-200/114 mmHg)."( Combination treatment with telmisartan and hydrochlorothiazide in black patients with mild to moderate hypertension.
McGill, JB; Reilly, PA, 2001
)
0.57
"A simple, rapid and sensitive HPLC method has been developed for the simultaneous determination of ramipril and hydrochlorothiazide in their dosage forms."( A stability-indicating LC method for the simultaneous determination of ramipril and hydrochlorothiazide in dosage forms.
Abounassif, MA; Al-Zaagi, IA; Belal, F; Gadkariem, EA, 2001
)
0.75
" In both treatment groups the dosage could be doubled after > or =2 weeks [according to blood pressure (BP) response] and, if necessary, subsequently decreased if the higher dosage was poorly tolerated."( Antihypertensive treatment in elderly patients aged 75 years or over: a 24-week study of the tolerability of candesartan cilexetil in relation to hydrochlorothiazide.
Forsén, B; Neldam, S, 2001
)
0.51
"First-derivative ultraviolet spectrophotometry and high-performance liquid chromatography (HPLC) were used to determine valsartan and hydrochlorothiazide simultaneously in combined pharmaceutical dosage forms."( Simultaneous determination of valsartan and hydrochlorothiazide in tablets by first-derivative ultraviolet spectrophotometry and LC.
Altinay, S; Göğer, NG; Ozkan, SA; Satana, E; Sentürk, Z, 2001
)
0.78
" The pharmacokinetic parameters of the drug post intravenous dosing were reported for the first time."( In vivo evaluation of hydrochlorothiazide liquisolid tablets in beagle dogs.
Asiri, YA; El-Sayed, YM; Khaled, KA, 2001
)
0.63
" It also examined the dose-response surface for the 2 drugs alone and in combination."( Telmisartan plus hydrochlorothiazide versus telmisartan or hydrochlorothiazide monotherapy in patients with mild to moderate hypertension: a multicenter, randomized, double-blind, placebo-controlled, parallel-group trial.
McGill, JB; Reilly, PA, 2001
)
0.65
" Chlorthiazide's toxic dose for 50% of animals tested (TD50) could not be achieved even with dosing as high as 1,500 mg/kg for furosemide; TD50 was 549 mg/kg."( Are certain diuretics also anticonvulsants?
Annegers, JF; Cascino, G; Hauser, WA; Hesdorffer, DC; Stables, JP, 2001
)
0.31
" In conclusion, switching to V/HCTZ combination therapy provides an additional lowering of BP compared to dosage increase of the thiazide in patients with BP insufficiently controlled by HCTZ 12."( Antihypertensive effects of valsartan/hydrochlorothiazide combination in essential hypertension.
Adam, SA; Handrock, R; Kolloch, R; Schmidt, A; Weidinger, G, 2001
)
0.58
"Sodium starch glycolate is a commonly used super-disintegrant employed to promote rapid disintegration and dissolution of IR solid dosage forms."( Multiple sources of sodium starch glycolate, NF: evaluation of functional equivalence and development of standard performance tests.
Augsburger, L; Shah, U, 2002
)
0.31
" Nevertheless, physicians are often reluctant to prescribe multiple anti-hypertensive drugs due to concerns over side-effects, inconvenient dosing regimens and costs."( A new fixed-dose combination for added blood pressure control: telmisartan plus hydrochlorothiazide.
Lacourcière, Y,
)
0.36
" Of those who received a dosage adjustment, a significantly greater percentage of amlodipine-treated patients (59%) than losartan/HCTZ-treated patients (42%) reached BP goal at the last visit (p=0."( The effects of amlodipine compared to losartan in patients with mild to moderately severe hypertension.
Grimm, RH; Kloner, RA; Phillips, RA; Weinberger, M,
)
0.13
" Irbesartan therapy at a dosage of 150300 mg was instituted as monotherapy or associated with hydrochlorothiazide, 12."( [Effect of anti-hypertensive therapy with irbesartan on the absolute cardiovascular risk].
Aranda, P; Calvo, C; Coca, A; de la Sierra, A; Luque, M; Marín-Iranzo, R; Ruilope, LM, 2003
)
0.54
" During the last six hours of the dosing interval, telmisartan 40 mg/HCTZ 12."( Efficacy and tolerability of fixed-dose combinations of telmisartan plus HCTZ compared with losartan plus HCTZ in patients with essential hypertension.
Byrne, M; Gil-Extremera, B; Lacourcière, Y; Mueller, O; Williams, L, 2003
)
0.32
" Both drugs provided effective control over the 24-h dosing interval."( Telmisartan vs losartan plus hydrochlorothiazide in the treatment of mild-to-moderate essential hypertension--a randomised ABPM study.
Kolloch, RE; Meinicke, TW; Neutel, JM; Plouin, PF; Schumacher, H, 2003
)
0.61
"5 mg) were evaluated for bioequivalence after single dosing in healthy volunteers."( Comparative bioavailability of two immediate-release tablets of lisinopril/hydrochlorothiazide in healthy volunteers.
Cuadrado, A; Dalmau, R; Gascón, AR; Hernández, RM; Pedraz, JL; Ramírez, E; Solinís, MA, 2003
)
0.55
" The daily dosage of triamterene ranged from 50 to 250 mg."( TREATMENT OF CONGESTIVE HEART FAILURE WITH TRIAMTERENE.
FRIEDMAN, R; SCHUCHER, R; WENER, J, 1965
)
0.24
" The drug's effect as well as adverse effects should be actively sought, and dosage alterations made in order to enhance the drug's effect."( Introduction to monitoring. What is what you prescribed actually doing?
George, A; Shakib, S, 2003
)
0.32
" Telmisartan is a highly selective blocker of angiotensin II AT1 receptors ("sartans"); it is at least as effective as the classical antihypertensive agents; thanks to its half-life, the longest of all sartans', it provides adequate antihypertensive coverage throughout the whole 24-hour postdose interval and particularly over the last 6 hours of the dosage interval."( [Kinzalkomb, a fixed telmisartan-hydrochlorothiazide combination for the treatment of hypertension].
Kulbertus, H, 2003
)
0.6
"001) and the other periods of the 24-h interval compared with the levels achieved by the previous treatment, indicating a clear dose-response relationship."( Antihypertensive effects of two fixed-dose combinations of losartan and hydrochlorothiazide versus hydrochlorothiazide monotherapy in subjects with ambulatory systolic hypertension.
Lacourcière, Y; Poirier, L, 2003
)
0.55
"5 and L 100/HCTZ 25 provided greater reductions in clinic and ABP than HCTZ monotherapies, with a clear dose-response relationship with regard to ABP."( Antihypertensive effects of two fixed-dose combinations of losartan and hydrochlorothiazide versus hydrochlorothiazide monotherapy in subjects with ambulatory systolic hypertension.
Lacourcière, Y; Poirier, L, 2003
)
0.55
" Good linearity, precision and selectivity were found, and the two methods were successfully applied to the pharmaceutical dosage form containing the above-mentioned drug combination without any interference by the excipients."( Application of first derivative UV-spectrophotometry and ratio derivative spectrophotometry for the simultaneous determination of candesartan cilexetil and hydrochlorothiazide.
Erk, N, 2003
)
0.52
" The obtained three dissolution profiles from one dosage form are the whole formulation profile or "global profile" recommended by pharmacopoeias, and, at same time, are recorded two "individual" profiles from two drugs present in the formulation."( Automated simultaneous triple dissolution profiles of two drugs, sulphamethoxazole-trimethoprim and hydrochlorothiazide-captopril in solid oral dosage forms by a multicommutation flow-assembly and derivative spectrophotometry.
Catalá Icardo, M; Martínez Calatayud, J; Tomsů, D, 2004
)
0.54
" Evaluation of the 24-h profiles showed evidence for sustained pharmacodynamic effects of telmisartan over the entire dosing period."( Ambulatory blood pressure monitoring in the primary care setting: assessment of therapy on the circadian variation of blood pressure from the MICCAT-2 Trial.
Bakris, GL; Davidai, G; Giles, T; Neutel, JM; Weber, MA; White, WB, 2005
)
0.33
" The relative bioavailability of two FDA approved (Orange Book AB rating) solid oral dosage forms of metoprolol and propranolol/hydrochlorothiazide (combination tablets) was evaluated in human volunteers under fed conditions using a two-way crossover design."( The effect of food on the relative bioavailability of rapidly dissolving immediate-release solid oral products containing highly soluble drugs.
Asafu-Adjaye, E; Ciavarella, AB; Conner, DP; Faustino, PJ; Hussain, AS; Lesko, LJ; Mehta, MU; Parekh, A; Straughn, AB; Yang, Y; Yu, LX,
)
0.34
"Four sensitive methods are described for the direct determination of telmisartan (TELM) and hydrochlorothiazide (HCT) in combined dosage forms without prior separation."( Application of first-derivative, ratio derivative spectrophotometry, TLC-densitometry and spectrofluorimetry for the simultaneous determination of telmisartan and hydrochlorothiazide in pharmaceutical dosage forms and plasma.
Abbas, SS; Bebawy, LI; Fattah, LA; Refaat, HH, 2005
)
0.74
" This suggests that, in patients with hypertension, it may be important to maintain the efficacy of antihypertensive medication over the 24-h dosing interval, especially in the risky early morning hours."( Telmisartan/Hydrochlorothiazide in comparison with losartan/hydrochlorothiazide in managing patients with mild-to-moderate hypertension.
Chrysant, SG; Littlejohn, TW; Neutel, JM; Singh, A, 2005
)
0.71
" The primary end point was the reduction from baseline in mean ambulatory DBP over the last 6 hours of the dosing interval."( Comparison of fixed-dose combinations of telmisartan/hydrochlorothiazide 40/12.5 mg and 80/12.5 mg and a fixed-dose combination of losartan/hydrochlorothiazide 50/12.5 mg in mild to moderate essential hypertension: pooled analysis of two multicenter, pros
Lacourcière, Y; Neutel, JM; Schumacher, H, 2005
)
0.58
"5, including during the last 6 hours of the dosing interval."( Comparison of fixed-dose combinations of telmisartan/hydrochlorothiazide 40/12.5 mg and 80/12.5 mg and a fixed-dose combination of losartan/hydrochlorothiazide 50/12.5 mg in mild to moderate essential hypertension: pooled analysis of two multicenter, pros
Lacourcière, Y; Neutel, JM; Schumacher, H, 2005
)
0.58
" Reduction in diastolic load was significantly greater with irbesartan/HCTZ than with losartan/HCTZ as was mean ambulatory systolic BP during the last 4 h of the dosing interval."( Ambulatory blood pressure comparison of the anti-hypertensive efficacy of fixed combinations of irbesartan/hydrochlorothiazide and losartan/hydrochlorothiazide in patients with mild-to-moderate hypertension.
Neutel, JM; Smith, D,
)
0.34
" The long elimination half-life of telmisartan ensures the drug provides effective reductions in blood pressure (BP) across the entire 24-hour dosage interval."( Telmisartan: a review of its use in the management of hypertension.
Battershill, AJ; Scott, LJ, 2006
)
0.33
" Twenty-four-hour ambulatory blood pressure monitoring showed that telmisartan plus HCTZ (n=448) and amlodipine plus HCTZ (n=424) changed systolic blood pressure for the last 6 hours of the dosing interval by -18."( Telmisartan plus HCTZ vs. amlodipine plus HCTZ in older patients with systolic hypertension: results from a large ambulatory blood pressure monitoring study.
Edwards, C; Neldam, S,
)
0.13
"Olmesartan medoxomil monotherapy at the recommended dosage of 20 mg once daily is effective and well tolerated in patients with mild-to-moderate hypertension."( Blood pressure reduction with olmesartan in mild-to-moderate essential hypertension: a planned interim analysis of an open label sub-study in German patients.
Böhm, M; Ewald, S, 2006
)
0.33
" Patients' dosing histories were compiled electronically (MEMS, AARDEX)."( Management of patients with uncontrolled arterial hypertension--the role of electronic compliance monitoring, 24-h ambulatory blood pressure monitoring and Candesartan/HCTZ.
Mengden, T; Tousset, E; Uen, S; Vetter, H, 2006
)
0.33
" In each study, subjects received multiple once-daily doses of aliskiren and the test antihypertensive drug alone or in combination in two dosing periods separated by a drug-free washout period."( Lack of pharmacokinetic interactions of aliskiren, a novel direct renin inhibitor for the treatment of hypertension, with the antihypertensives amlodipine, valsartan, hydrochlorothiazide (HCTZ) and ramipril in healthy volunteers.
Bizot, MN; Denouel, J; Dieterich, HA; Dole, WP; Kemp, C; Vaidyanathan, S; Valencia, J; Yeh, CM; Zhao, C, 2006
)
0.53
"These results show that there is little or no potential for a clinically relevant pharmacokinetic interaction between olmesartan medoxomil 20 mg and hydrochlorothiazide 25 mg, and therefore dosage adjustment should not be necessary when they are co-administered."( Pharmacokinetics of olmesartan medoxomil plus hydrochlorothiazide combination in healthy subjects.
Bolbrinker, J; Huber, M; Kreutz, R, 2006
)
0.79
" Changes in DBP and SBP were fitted to a first-order dose-response surface (lack-of-fit test, P = ."( Aliskiren, an orally effective renin inhibitor, provides antihypertensive efficacy alone and in combination with valsartan.
Aldigier, JC; Azizi, M; Chiang, Y; Januszewicz, A; Pool, JL; Satlin, A; Schmieder, RE; Zidek, W, 2007
)
0.34
" In addition, combination therapy provided sustained and consistent BP control over the entire 24 hour dosing interval."( Fixed combination of zofenopril plus hydrochlorothiazide in the management of hypertension: a review of available data.
Borghi, C; Cicero, AF, 2006
)
0.61
" The primary endpoint was change from baseline in mean ambulatory systolic and diastolic blood pressure (SBP; DBP) during the last 6 hours of the 24-hour dosing interval."( Telmisartan/hydrochlorothiazide versus valsartan/hydrochlorothiazide in obese hypertensive patients with type 2 diabetes: the SMOOTH study.
Davidson, J; Koval, S; Lacourcière, Y; Sharma, AM, 2007
)
0.72
"In high-risk, overweight/obese patients with hypertension and type 2 diabetes, T/HCTZ provides significantly greater BP lowering versus V/HCTZ throughout the 24-hour dosing interval, particularly during the hazardous early morning hours."( Telmisartan/hydrochlorothiazide versus valsartan/hydrochlorothiazide in obese hypertensive patients with type 2 diabetes: the SMOOTH study.
Davidson, J; Koval, S; Lacourcière, Y; Sharma, AM, 2007
)
0.72
" Overall, no linear dose-response relationship was observed."( BP goal achievement in patients with uncontrolled hypertension : results of the treat-to-target post-marketing survey with irbesartan.
Bramlage, P; Lüders, S; Paar, DW; Schirmer, A; Schrader, J; Thoenes, M, 2007
)
0.34
" We can conclude that the results obtained in this study support an option of tablet splitting, which is very important for obtaining the required dosage when a dosage form of the required strength is unavailable, and for better individualization of the therapy."( Influence of tablet splitting on content uniformity of lisinopril/hydrochlorthiazide tablets.
Uzunović, A; Vranić, E, 2007
)
0.34
" Likewise, few studies have directly compared more than two agents or ARB/hydrochlorothiazide fixed-dose combinations, and most ARBs have not been compared across their full recommended dosage ranges."( Comparison of angiotensin II type 1 receptor antagonists in the treatment of essential hypertension.
Smith, DH, 2008
)
0.58
" Notably, BP control is sustained throughout the 24-hour dosage interval, including during the last 4 hours of this period."( Olmesartan medoxomil: a review of its use in the management of hypertension.
McCormack, PL; Scott, LJ, 2008
)
0.35
" In addition, a dose-response was observed with increasing dose of HCTZ with respect to MSSBP."( Combination therapy with valsartan/hydrochlorothiazide at doses up to 320/25 mg improves blood pressure levels in patients with hypertension inadequately controlled by valsartan 320 mg monotherapy.
Baumgart, P; Ferber, P; Le Breton, S; Reimund, B; Tuomilehto, J; Tykarski, A, 2008
)
0.62
"Two analytical methods have been developed for simultaneous quantification of bisoprolol fumarate and hydrochlorothiazide in combined pharmaceutical dosage form using spectrophotometer."( Simultaneous spectrophotometric estimation of Bisoprolol fumarate and hydrochlorothiazide in tablet dosage form.
A, SA; J, SS; R, TR, 2008
)
0.8
"Simple, accurate, economical, and reproducible UV spectrophotometric and column high-performance liquid chromatographic (HPLC) methods were developed for simultaneous estimation of a 2-component drug mixture of metoprolol tartrate and hydrochlorothiazide in combined tablet dosage form."( Spectrophotometric and column high-performance liquid chromatographic methods for simultaneous estimation of metoprolol tartrate and hydrochlorothiazide in tablets.
Garg, G; Saraf, S,
)
0.52
"Two simple and accurate methods for analysis of nebivolol hydrochloride (NEB) and hydrochlorothiazide (HCTZ) in their combined dosage forms were developed using first-order derivative spectrophotometry and reversed-phase liquid chromatography (LC)."( Determination of nebivolol hydrochloride and hydrochlorothiazide in tablets by first-order derivative spectrophotometry and liquid chromatography.
Baldania, SL; Bhatt, KK; Mehta, RS; Shah, DA,
)
0.62
"A simple, rapid, and precise method was developed for the quantitative simultaneous determination of telmisartan and hydrochlorothiazide in combined pharmaceutical dosage form."( Simultaneous high-performance liquid chromatographic determination of telmisartan and hydrochlorothiazide in pharmaceutical preparation.
Rane, VP; Sangshetti, JN; Shinde, DB,
)
0.56
"Tablets are one of the most popular and preferred solid dosage forms because they can be accurately dosed, easily manufactured and packaged on a large scale, have good physical and chemical stability, and can contribute to good patient compliance given their ease of administration."( Comparison of some physical parameters of whole and scored lisinopril and lisinopril/hydrochlorthiazide tablets.
Uzunović, A; Vranić, E, 2008
)
0.35
" Dosing regimens are either not executed as prescribed (noncompliance) or patients stop taking the medication (nonpersistence)."( Impact of supportive measures on drug adherence in patients with essential hypertension treated with valsartan: the randomized, open-label, parallel group study VALIDATE.
Düsing, R; Handrock, R; Klebs, S; Tousset, E; Vrijens, B, 2009
)
0.35
" In parallel, execution of the dosing regimen (compliance) was also improved in the intervention group during the early months of treatment but this effect also disappeared by the end of the observation period."( Impact of supportive measures on drug adherence in patients with essential hypertension treated with valsartan: the randomized, open-label, parallel group study VALIDATE.
Düsing, R; Handrock, R; Klebs, S; Tousset, E; Vrijens, B, 2009
)
0.35
" After a 4-week wash-out period, 209 patients were randomized to either CC 8 mg or AML 5 mg once daily for a minimum of 1 month, after which, if BP was not normalized, the dosage was doubled, followed by the addition of hydrochlorothiazide 12."( Effects of candesartan cilexetil on carotid remodeling in hypertensive diabetic patients: the MITEC study.
Asmar, R; Baguet, JP; Mallion, JM; Nisse-Durgeat, S; Valensi, P, 2009
)
0.54
"To describe the antihypertensive dose-response of combination therapy with candesartan and hydrochlorothiazide (HCT)."( A dose-response analysis of candesartan-hydrochlorothiazide combination therapy in patients with hypertension.
Elmfeldt, D; Karlson, BW; Olofsson, B; Zetterstrand, S, 2009
)
0.84
" An E(max) model was used to describe the placebo-adjusted dose-response surface for systolic and diastolic blood pressure (BP) reductions."( A dose-response analysis of candesartan-hydrochlorothiazide combination therapy in patients with hypertension.
Elmfeldt, D; Karlson, BW; Olofsson, B; Zetterstrand, S, 2009
)
0.62
" Despite optimal dosing of HCTZ + atenolol, only two-thirds of the participants achieved BP control."( Hydrochlorothiazide and atenolol combination antihypertensive therapy: effects of drug initiation order.
Bailey, KR; Beitelshees, AL; Boerwinkle, E; Campbell, K; Chapman, AB; Cooper-DeHoff, RM; Gong, Y; Gums, JG; Johnson, JA; Schmidt, S; Schwartz, GL; Turner, ST, 2009
)
1.8
"Two simple, economical, rapid, precise, and accurate methods for simultaneous determination of olmesartan medoxomil and hydrochlorothiazide in combined tablet dosage form have been developed."( Ratio spectra derivative and zero-crossing difference spectrophotometric determination of olmesartan medoxomil and hydrochlorothiazide in combined pharmaceutical dosage form.
Bari, PD; Rote, AR, 2009
)
0.77
" In large, randomized trials, eprosartan (with or without hydrochlorothiazide [HCTZ]) demonstrated superior antihypertensive efficacy to that of placebo and, when administered at comparable dosage regimens, had similar blood pressure-lowering effects to enalapril."( Eprosartan: a review of its use in hypertension.
Plosker, GL, 2009
)
0.6
"A simple, precise and stability-indicating HPLC method was developed and validated for the simultaneous determination of bisoprolol fumarate and hydrochlorothiazide in pharmaceutical dosage form."( RP-HPLC method for simultaneous estimation of bisoprolol fumarate and hydrochlorothiazide in tablet formulation.
Bhoir, SI; Bindu, KS; Das, C; Joshi, SJ; Karbhari, PA, 2010
)
0.79
"5 mg (V/HCTZ), and electively titrated after weeks 2 and 4 to the next dosage level (maximum dose valsartan/HCTZ 160/25 mg) if BP remained >140/90 mm Hg."( Effectiveness of initiating treatment with valsartan/hydrochlorothiazide in patients with stage-1 or stage-2 hypertension.
Calhoun, DA; Jamerson, KA; Palmer, BF; Purkayastha, D; Samuel, R; Zappe, DH, 2010
)
0.61
"After oral administration of low, middle, high dose of simulative Maijunan tablets to SD rats and puerarin, hydrochlorothiazide at middle dosage to SD rats separately, plasma samples were collected at different times and treated with acetonitrile to precipitate protein."( [Pharmacokinetics of puerarin and hydrochlorothiazide from maijunan tablets in rats].
Chen, Y; Du, P; Han, FM; Zhang, X, 2009
)
0.84
" Secondary endpoints included: change in ambulatory diastolic BP (DBP) from baseline to Week 12; changes in ambulatory SBP and DBP during daytime, nighttime, and the last 2, 4, and 6 hours of the dosing interval; and achievement of prespecified ambulatory BP targets."( Effects of an olmesartan medoxomil based treatment algorithm on 24-hour blood pressure control in patients with hypertension and type 2 diabetes.
Kereiakes, DJ; Neutel, JM; Shojaee, A; Stoakes, KA; Waverczak, WF; Xu, J, 2010
)
0.36
" We sought to describe their comparative dose-response relationships for changes in systolic blood pressure (SBP) and potassium."( Meta-analysis of dose-response characteristics of hydrochlorothiazide and chlorthalidone: effects on systolic blood pressure and potassium.
Carter, BL; Ernst, ME; Grimm, RH; Zheng, S, 2010
)
0.61
" Data were pooled to evaluate the effects on SBP and potassium of both drugs throughout their respective dose-response curves."( Meta-analysis of dose-response characteristics of hydrochlorothiazide and chlorthalidone: effects on systolic blood pressure and potassium.
Carter, BL; Ernst, ME; Grimm, RH; Zheng, S, 2010
)
0.61
" However, within this dosing range, reductions in potassium can be considered equivalent."( Meta-analysis of dose-response characteristics of hydrochlorothiazide and chlorthalidone: effects on systolic blood pressure and potassium.
Carter, BL; Ernst, ME; Grimm, RH; Zheng, S, 2010
)
0.61
"To evaluate the therapeutic effects of combination administration of hydrochlorothiazide and nitrendipine at low dosage in the treatment of rural hypertension patients."( [Analysis of therapeutic effects of rural patients with hypertension by combination administration of low dosage of hydrochlorothiazide and nitrendipine].
Hu, DY; Li, J; Liu, SS; Sun, YX; Sun, ZQ; Xu, CL; Zhang, DY; Zhang, XG; Zhang, XZ; Zheng, LQ, 2010
)
0.8
"A simple and precise stability-indicating liquid chromatography method is developed and validated for the quantitative simultaneous estimation of irbesartan (IRB) and hydrochlorothiazide (HCTZ) in combined pharmaceutical dosage form."( Stability indicating LC method for simultaneous determination of irbesartan and hydrochlorothiazide in pharmaceutical preparations.
Patil, KR; Rane, VP; Sangshetti, JN; Shinde, DB; Yeole, RD, 2010
)
0.78
" The validated HPLC methods were successfully applied to the analysis of their commercial tablet dosage forms, for which no interfering peaks were encountered from common pharmaceutical adjuvants."( Validated HPLC determination of the two fixed dose combinations (chlordiazepoxide hydrochloride and mebeverine hydrochloride; carvedilol and hydrochlorothiazide) in their tablets.
Belal, TS; Haggag, RS; Shaalan, RA,
)
0.33
" In conclusion, adding HCTZ to OM 40 mg significantly improves BP reductions and target BP rates in harder-to-treat patients and a clear dose-response was observed for efficacy."( Effects of high dose olmesartan medoxomil plus hydrochlorothiazide on blood pressure control in patients with grade 2 and grade 3 hypertension.
Girerd, X; Rump, LC; Sellin, L; Stegbauer, J, 2011
)
0.63
" This study included 15 subjects whose therapy was changed from a usual dosage of ARB to losartan 50mg/HCTZ 12."( Effects of losartan/hydrochlorothiazide treatment, after change from ARB at usual dosage, on blood pressure and various metabolic parameters including high-molecular weight adiponectin in Japanese male hypertensive subjects.
Hirose, H; Kawabe, H; Saito, I, 2011
)
0.69
" The effect of chronic aspirin and HCTZ dosing taken together upon the efficacy of chronic allopurinol therapy in patients with hyperuricaemia needs to be investigated."( Lack of effect of hydrochlorothiazide and low-dose aspirin on the renal clearance of urate and oxypurinol after a single dose of allopurinol in normal volunteers.
Day, RO; Graham, GG; Ng, DY; Stocker, SL; Williams, KM, 2011
)
0.7
" Once-daily treatment with amlodipine/valsartan/hydrochlorothiazide (10/320/25 mg) reduces ABP to a significantly greater extent than component-based dual therapy and maintains its effectiveness over the entire 24-h dosing period."( 24-Hour ambulatory blood pressure control with triple-therapy amlodipine, valsartan and hydrochlorothiazide in patients with moderate to severe hypertension.
Calhoun, DA; Crikelair, N; Glazer, RD; Lacourcière, Y; Yen, J, 2011
)
0.85
"Two simple, accurate and reproducible spectrophotometric methods have been developed for the simultaneous estimation of Hydrochlorothiazide (Hctz), Atenolol (Atn) and Losartan potassium (Los) in combined tablet dosage forms."( Simultaneous spectrophotometric estimation of Hydrochlorothiazide, Atenolol and Losartan potassium in tablet dosage form.
Chavan, UB; Deshpande, AD; Dighe, SB; Jagdale, SN; Kothapalli, LP; Nanda, RK; Thomas, AB, 2009
)
0.82
"The new European regulations on paediatric medicines and recent WHO recommendations have induced an increased need for research into novel child-appropriate dosage forms."( Orally disintegrating mini-tablets (ODMTs)--a novel solid oral dosage form for paediatric use.
Breitkreutz, J; Stoltenberg, I, 2011
)
0.37
" In conclusion, this amlodipine/OM-based titration regimen was well tolerated and effectively lowered BP throughout the 24-hour dosing interval in patients with hypertension and type 2 diabetes."( Management of hypertension in patients with diabetes using an amlodipine-, olmesartan medoxomil-, and hydrochlorothiazide-based titration regimen.
Littlejohn, T; Neutel, JM; Qian, C; Ram, CV; Sachson, R; Shojaee, A; Stoakes, KA, 2011
)
0.58
" Secondary efficacy endpoints included the change from baseline in mean 24-hour ambulatory SBP; change from baseline in ambulatory BP during the daytime (8:00 am-4:00 pm), nighttime (10:00 pm-6:00 am) and the last 6, 4 and 2 hours of the dosing interval; change from baseline in SeBP at each titration step and at study end; and the proportion of patients achieving mean 24-hour ambulatory BP targets and SeBP goals at week 12."( Blood pressure-lowering efficacy of an olmesartan medoxomil/hydrochlorothiazide-based treatment algorithm in elderly patients (age ≥65 years) stratified by age, sex and race: subgroup analysis of a 12-week, open-label, single-arm, dose-titration study.
Kereiakes, DJ; Maa, JF; Neutel, J; Shojaee, A; Stoakes, KA; Waverczak, WF, 2011
)
0.61
" Clinically significant ambulatory BP reductions were observed during the daytime, nighttime and the last 6, 4 and 2 hours of the dosing interval in all subgroups."( Blood pressure-lowering efficacy of an olmesartan medoxomil/hydrochlorothiazide-based treatment algorithm in elderly patients (age ≥65 years) stratified by age, sex and race: subgroup analysis of a 12-week, open-label, single-arm, dose-titration study.
Kereiakes, DJ; Maa, JF; Neutel, J; Shojaee, A; Stoakes, KA; Waverczak, WF, 2011
)
0.61
" The proposed MEKC method was successfully applied for the quantitative analysis of ALI and HCTZ both individually and in a combined dosage tablet formulation to support the quality control."( Simultaneous determination of aliskiren and hydrochlorothiazide from their pharmaceutical preparations using a validated stability-indicating MEKC method.
Oliveira, PR; Rolim, CM; Sangoi, MS; Steppe, M; Wrasse-Sangoi, M, 2011
)
0.63
"In this ABPM substudy (n=108), initiation of treatment with valsartan/hydrochlorothiazide lowered ABP more effectively than either monotherapy throughout the daytime, night-time, and 24-h monitoring periods, as well as during the last 4 and 6-h dosing periods."( Effect of valsartan, hydrochlorothiazide, and their combination on 24-h ambulatory blood pressure response in elderly patients with systolic hypertension: a ValVET substudy.
Cushman, WC; Duprez, DA; Izzo, JL; Purkayastha, D; Samuel, R; Weintraub, HS; Zappe, D, 2011
)
0.92
"Administration of angiotensin receptor blockers at bedtime results in greater reduction of nighttime blood pressure than dosing upon awakening, independent of the terminal half-life of each individual medication."( Chronotherapy with valsartan/hydrochlorothiazide combination in essential hypertension: improved sleep-time blood pressure control with bedtime dosing.
Ayala, DE; Fernández, JR; Fontao, MJ; Hermida, RC; Mojón, A, 2011
)
0.66
" Greater efficacy was also found during daytime and nighttime hours and during the last 6, 4, or 2 hours of the dosing interval."( 24-hour efficacy and safety of Triple-Combination Therapy With Olmesartan, Amlodipine, and Hydrochlorothiazide: the TRINITY ambulatory blood pressure substudy.
Chrysant, SG; Fernandez, V; Heyrman, R; Izzo, JL; Kereiakes, DJ; Lee, J; Littlejohn Iii, T; Melino, M; Oparil, S, 2011
)
0.59
"6 mmHg), ABP in the last 4 hours of the dosing period (-21."( Ambulatory blood pressure response to triple therapy with an angiotensin-receptor blocker (ARB), calcium-channel blocker (CCB), and HCTZ versus dual therapy with an ARB and HCTZ.
Duprez, D; Ferdinand, K; Purkayastha, D; Samuel, R; Wright, R, 2011
)
0.37
" Cumulative urine samples were collected predosing and over 24 h after dosing in each period to compare urine electrolyte excretion profiles of potassium (UKV), sodium (UNaV), magnesium, calcium, phosphate, chloride, and pH among groups."( A comparison of the natriuretic and kaliuretic effects of cicletanine and hydrochlorothiazide in prehypertensive and hypertensive humans.
Beals, C; Carey, RM; De Lepeleire, I; Fernandez, R; Gildea, J; Greenwalt, DM; Johnson-Levonas, AO; Malice, MP; McGrath, HE; Mitta, S; Nunes, I; Sisk, CM; Van Dyck, K; Wagner, F; Wiegert, E, 2012
)
0.61
"Experimental design method was used for HPLC determination of irbesartan and hydrochlorothiazide in combined dosage forms."( Simultaneous analysis of irbesartan and hydrochlorothiazide: an improved HPLC method with the aid of a chemometric protocol.
Brborić, J; Mulavdić, N; Smajić, M; Stankovic, P; Vujić, Z, 2012
)
0.88
" In this report, no significant correlations between dosage of hydrochlorothiazide and calciuria and no significant correlations between proteinuria and dosage of enalapril were detected."( The long-term use of enalapril and hydrochlorothiazide in two novel mutations patients with Dent's disease type 1.
Henriques, Ldos S; Igarashi, T; Koch, VH; Seki, G; Sekine, T; Vaisbich, MH, 2012
)
0.9
"The aim of this study was to develop a multilayer (core/coat) dosage form via co-extrusion, the core providing sustained drug release and the coat immediate drug release."( Co-extrusion as manufacturing technique for fixed-dose combination mini-matrices.
Almeida, A; De Beer, T; Dierickx, L; Remon, JP; Saerens, L; Vervaet, C, 2012
)
0.38
" Home BP monitoring, if done with proper technique, provides a reliable indicator of BP control in elderly patients and may help guide drug dosing and titration."( Home and clinic blood pressure responses in elderly individuals with systolic hypertension.
Cushman, WC; Duprez, DA; Izzo, JL; Purkayastha, D; Samuel, R; Weintraub, HS; Zappe, D,
)
0.13
" We performed a meta-analysis to characterize the dose-response relationships for 3 commonly prescribed thiazide diuretics, hydrochlorothiazide, chlorthalidone, and bendroflumethiazide, on BP, serum potassium, and urate."( Meta-analysis of dose-response relationships for hydrochlorothiazide, chlorthalidone, and bendroflumethiazide on blood pressure, serum potassium, and urate.
Chaturvedi, N; Hardy, R; Hughes, AD; Peterzan, MA, 2012
)
0.84
"A simple, specific, accurate and precise stability-indicating reversed-phase high-performance liquid chromatographic method was developed for simultaneous estimation of olmesartan medoxomile (OLME), amlodipine besylate (AMLO) and hydrochlorothiazide (HCTZ) in tablet dosage form."( Stability-indicating method for simultaneous estimation of olmesartan medoxomile, amlodipine besylate and hydrochlorothiazide by RP-HPLC in tablet dosage form.
Chaudhari, AJ; Gorle, AP; Jain, PS; Patel, MK; Surana, SJ, 2012
)
0.78
"The current manuscript reports the first capillary electrophoresis method for the separation and quantification of metoprolol (MET) and hydrochlorothiazide (HCT) in their combined dosage form."( Capillary electrophoresis assay method for metoprolol and hydrochlorothiazide in their combined dosage form with multivariate optimization.
Aldughaish, AM; Alnajjar, AO; Attimarad, MV; Elgorashe, RE; Idris, AM, 2013
)
0.84
"An OM/HCTZ-based titration regimen enabled elderly patients with hypertension to safely reduce BP throughout the 24-hour dosing interval and allowed the majority of these patients to achieve a BP target of <140/90 mmHg or <140 mmHg."( Efficacy of olmesartan medoxomil and hydrochlorothiazide fixed-dose combination therapy in patients aged 65 years and older with stage 1 and 2 hypertension or isolated systolic hypertension.
Chavanu, KJ; Dubiel, R; Germino, FW; Maa, JF; Neutel, JM, 2012
)
0.65
" The single pill triple combination of aliskiren, amlodipine, and hydrochlorothiazide offers five different formulations of escalating dosages of the three agents, allowing dosing flexibility."( The single pill triple combination of aliskiren, amlodipine, and hydrochlorothiazide in the treatment of hypertension.
Huan, Y; Townsend, R, 2012
)
0.85
"Two reversed phase liquid chromatographic (RP-LC) techniques are presented for the rapid, accurate, precise, simultaneous determination of olmesartan-hydrochlorothiazide and zofenopril-hydrochlorothiazide binary mixtures in their dosage forms."( Simultaneous estimation and validation of some binary mixtures of antihypertensive drugs by RP-LC methods using two new generation silica columns.
Gumustas, M; Kurbanoglu, S; Ozkan, SA, 2013
)
0.59
" This study examined the practical efficacy of a combination therapy of ARB with thiazide diuretics for lowering morning home blood pressure (MHBP) in comparison to high-dose ARB therapy in patients with morning hypertension administered an ordinal dosage of ARB."( Losartan/hydrochlorothiazide combination therapy surpasses high-dose angiotensin receptor blocker in the reduction of morning home blood pressure in patients with morning hypertension.
Hanayama, Y; Makino, H; Nakamura, Y; Uchida, HA, 2012
)
0.8
"Accurate, sensitive and reproducible reversed-phase high-performance liquid chromatography (RP-HPLC), high-performance thin-layer chromatography (HPTLC) and ultraviolet (UV) spectrophopometric methods were developed for the concurrent estimation of amlodipine besylate (AMLO), hydrochlorothiazide (HCTZ) and valsartan (VALS) in bulk and combined tablet dosage forms."( Concurrent estimation of amlodipine besylate, hydrochlorothiazide and valsartan by RP-HPLC, HPTLC and UV-spectrophotometry.
Kothari, C; Mehta, P; Sharma, M; Sherikar, O, 2014
)
0.84
" An additional aim is to assess the effect of the polypill on LDL-c and BP compared to the administration of separate pills of identically dosed components of the polypill."( The evening versus morning polypill utilization study: the TEMPUS rationale and design.
Bots, ML; Grobbee, DE; Lafeber, M; Rodgers, A; Spiering, W; Thom, S; Visseren, FL; Webster, R, 2014
)
0.4
"5 mg) in the evening; (2) the polypill in the morning; and (3) the use of the identically dosed agents in separate pills taken at different time points during the day."( The evening versus morning polypill utilization study: the TEMPUS rationale and design.
Bots, ML; Grobbee, DE; Lafeber, M; Rodgers, A; Spiering, W; Thom, S; Visseren, FL; Webster, R, 2014
)
0.4
" Control of blood pressure with fixed dose combination of the above drugs acting through different mechanism have a benefit of convenient dosing in terms of compliance, lower the dose and subsequently reduce the side effects."( A comparative pharmacokinetic study of a fixed dose combination for essential hypertensive patients: a randomized crossover study in healthy human volunteers.
Biswas, E; Choudhury, H; Ghosh, B; Gorain, B; Halder, D; Pal, TK; Sarkar, AK; Sarkar, P, 2013
)
0.39
"5 mg) (ARB+D; n = 72) or a combination of amlodipine (5 mg) and the typical dosage of ARBs (ARB+C; n = 68) to evaluate the change in the BP, laboratory values and cognitive function."( Combination of antihypertensive therapy in the elderly, multicenter investigation (CAMUI) trial: results after 1 year.
Hasebe, N; Kikuchi, K; Koyama, S; Maruyama, J; Morimoto, H; Morita, K; Saijo, Y; Sano, H; Sasagawa, Y; Sato, N; Sumitomo, K; Takehara, N; Takeuchi, T, 2013
)
0.39
" All the proposed methods were effectively applied for the simultaneous determination of BIS and HCZ in tablet dosage forms without any time-consuming extraction, sample preparation, or derivatization procedures."( Fully validated simultaneous determination of bisoprolol fumarate and hydrochlorothiazide in their dosage forms using different voltammetric, chromatographic, and spectrophotometric analytical methods.
Bozal, B; Dogan-Topal, B; Gumustas, M; Ozkan, SA; Uslu, B,
)
0.37
" Our data show that CTL is associated with greater reduction in 24 h UCa compared to similarly dosed HCTZ."( Hydrochlorothiazide compared to chlorthalidone in reduction of urinary calcium in patients with kidney stones.
Astor, BC; Gundu, V; Jhagroo, RA; Wolfgram, DF, 2013
)
1.83
"In 88 patients (age 70 ± 12 years), ARB treatment was switched to the combination therapy (same dosage ARB+12."( Low salt intake and changes in serum sodium levels in the combination therapy of low-dose hydrochlorothiazide and angiotensin II receptor blocker.
Aizawa, Y; Fujii, Y; Hokama, Y; Kuwajima, I; Nakayama, M; Nakayama, T; Saito, T; Shimizu, T; Tomiyama, H; Yamashina, A, 2013
)
0.61
" Model diagnostics helped to demonstrate that the population PK model reasonably predicts the rate of urinary HCTZ excretion over time using dosing history and estimated CLCR , allowing for the convenient assessment of PK-PD relationships for HCTZ when given alone or in combination with other agents used to treat fluid overload conditions."( Population-based meta-analysis of hydrochlorothiazide pharmacokinetics.
Mager, DE; Mallikaarjun, S; Shoaf, SE; Van Wart, SA, 2013
)
0.67
"01), hydrochlorothiazide dosing did not significantly change over the study period."( Initial experience using aminophylline to improve renal dysfunction in the pediatric cardiovascular ICU.
Anglemyer, AT; Axelrod, DM; Grimm, PC; Roth, SJ; Sherman-Levine, SF; Sutherland, SM; Zhu, A, 2014
)
0.92
" The validated CE method was successfully applied to the analysis of two commercial tablet dosage forms."( Validated stability-indicating capillary electrophoresis method for the separation and determination of a fixed-dose combination of carvedilol and hydrochlorothiazide in tablets.
Al-Shehri, MM; Alzoman, NZ; Maher, HM; Olah, IV; Sultan, MA,
)
0.33
"A simple and rapid stability-indicating liquid chromatographic method was developed and validated for the simultaneous determination of lisinopril and hydrochlorotiazide (HCTZ) in drug substances and dosage forms in the presence of degradation products."( Stability-indicating LC method for the simultaneous determination of lisinopril and hydrochlorothiazide.
de Diego, M; Mennickent, S; Soto, J,
)
0.36
" The methods were used for the quantitative analysis of the drugs in raw materials and pharmaceutical dosage form via handling the UV spectral data."( Different approaches in Partial Least Squares and Artificial Neural Network models applied for the analysis of a ternary mixture of Amlodipine, Valsartan and Hydrochlorothiazide.
Darwish, HW; El-Zeany, BA; Hassan, SA; Salem, MY, 2014
)
0.6
"The combination of traditional Chinese medicines and chemical drugs may provide a promising strategy and unique advantages to reduce the dosage and side effects of chemical drugs while maintaining an effect on hypertension."( Enhanced absorption and bioavailability of hydrochlorothiazide by Chinese medicines in the Zhenju antihypertensive compound.
Bai, Y; Han, L; Jing, Y; Li, Y; Qin, J; Wang, J; Wang, L, 2014
)
0.67
"An alternative method for analysis of aliskiren (ALI) and hydrochlorothiazde (HCT) in combined dosage forms by ion-pair reversed phase high performance liquid chromatography was developed and validated."( Simultaneous determination of aliskiren and hydrochlorothiazide in tablets and spiked human urine by ion-pair liquid chromatography.
Belal, F; El-Enany, N; Walash, M; Zayed, S, 2013
)
0.65
" In stage 2, half of 28 subjects were daily dosed with regimen C for 7 days."( Pharmacokinetics and tolerability of olmesartan medoxomil plus hydrochlorothiazide combination in healthy Chinese subjects: drug-drug interaction, bioequivalence, and accumulation.
Hu, P; Jiang, J; Liu, DY; Wang, CG; Zhang, JY, 2014
)
0.64
" The developed method is suitable for the quality control and routine analysis of the cited drugs in their pharmaceutical dosage forms."( Synchronized separation of seven medications representing most commonly prescribed antihypertensive classes by using reversed-phase liquid chromatography: Application for analysis in their combined formulations.
Ebeid, WM; El-Bagary, RI; El-Zaher, AA; Elkady, EF; Patonay, G, 2014
)
0.4
" The specificity of the developed methods is investigated by analyzing laboratory prepared mixtures containing different ratios of the three drugs and their combined dosage form."( Spectrophotometric methods for simultaneous determination of ternary mixture of amlodipine besylate, olmesartan medoxomil and hydrochlorothiazide.
Diab, SS; Merey, HA; Moustafa, AA; Ramadan, NK, 2014
)
0.61
"A novel, specific, reliable, and accurate capillary zone electrophoretic method was developed and validated for the simultaneous determination of aliskiren hemifumarate, amlodipine besylate, and hydrochlorothiazide in their triple mixture dosage form."( Simultaneous determination of aliskiren hemifumarate, amlodipine besylate, and hydrochlorothiazide in their triple mixture dosage form by capillary zone electrophoresis.
Belal, F; Ebeid, WM; El-Enany, N; Patonay, G; Salim, MM; Walash, M, 2014
)
0.82
"Characterisation of the effect of food on the bio-performance of modified and extended release dosage forms can be very challenging due to the need to replicate the dynamic biochemical conditions of the human gut as well as the complex physical processing modalities under fed state."( Application of the Dynamic Gastric Model to evaluate the effect of food on the drug release characteristics of a hydrophilic matrix formulation.
Chessa, S; Ferrizzi, D; Huatan, H; Levina, M; Mehta, RY; Rajabi-Siahboomi, AR, 2014
)
0.4
" Moreover, the methods were successfully applied for the determination of HCZ and BZ and AM in pure form and pharmaceutical dosage forms."( Simultaneous determination of hydrochlorothiazide and benazepril hydrochloride or amiloride hydrochloride in presence of hydrochlorothiazide impurities: chlorothiazide and salamide by HPTLC method.
Abdelaleem, EA; Draz, ME; Naguib, IA; Zaazaa, HE, 2015
)
0.71
" The analysis results prove to be valid for analysis of the two active ingredients in raw materials and pharmaceutical dosage form through handling UV spectral data in range (220-350 nm)."( Linear support vector regression and partial least squares chemometric models for determination of Hydrochlorothiazide and Benazepril hydrochloride in presence of related impurities: a comparative study.
Abdelaleem, EA; Draz, ME; Naguib, IA; Zaazaa, HE, 2014
)
0.62
" Data was pooled separately for the two T40 non-responder studies (T40 NR group, two T80 non-responder studies (T80 NR group), and the two factorial design dose-response studies (FD-DR group)."( Telmisartan in combination with hydrochlorothiazide 12.5 mg for the management of patients with hypertension.
Kjeldsen, SE; Neldam, S; Neutel, JM; Schumacher, H, 2014
)
0.69
"Hydrophilic matrix tablets are commonly used for extended release dosage forms."( Application of ethylcellulose coating to hydrophilic matrices: a strategy to modulate drug release profile and reduce drug release variability.
Mehta, RY; Missaghi, S; Rajabi-Siahboomi, AR; Tiwari, SB, 2014
)
0.4
"A simple, sensitive and accurate HPLC method with high throughput has been developed and validated for the simultaneous determination of irbesartan (IRB) and hydrochlorothiazide (HCT) in combined pharmaceutical dosage forms."( HPLC method with monolithic column for simultaneous determination of irbesartan and hydrochlorothiazide in tablets.
Abdelhameed, AS; Alanazi, AM; Darwish, IA; Khalil, NY; Khan, AA, 2014
)
0.82
"Three simple, accurate, reproducible, and selective methods have been developed and subsequently validated for the simultaneous determination of Moexipril (MOX) and Hydrochlorothiazide (HCTZ) in pharmaceutical dosage form."( Comparative study between univariate spectrophotometry and multivariate calibration as analytical tools for simultaneous quantitation of Moexipril and Hydrochlorothiazide.
Elaziz, OA; Farouk, M; Hemdan, A; Shehata, MA; Tawakkol, SM, 2014
)
0.8
"This study focused on the evaluation of prilling as a technique for the manufacturing of multiparticulate dosage forms."( Prilling as manufacturing technique for multiparticulate lipid/PEG fixed-dose combinations.
De Beer, T; Monteyne, T; Remon, JP; Saerens, L; Vervaeck, A; Vervaet, C, 2014
)
0.4
"Studies suggest that bedtime dosing of an angiotensin-converting enzyme (ACE)-inhibitor or angiotensin receptor blocker shows a more sustained and consistent 24-h antihypertensive profile, including greater night-time blood pressure (BP) reduction."( Time of administration important? Morning versus evening dosing of valsartan.
Crikelair, N; Kandra, A; Palatini, P; Zappe, DH, 2015
)
0.42
" Evening dosing also did not improve BP lowering in patients requiring add-on HCTZ or in nondippers at baseline."( Time of administration important? Morning versus evening dosing of valsartan.
Crikelair, N; Kandra, A; Palatini, P; Zappe, DH, 2015
)
0.42
"Once-daily dosing of valsartan 320 mg results in equally effective 24-h BP efficacy, regardless of dosing time."( Time of administration important? Morning versus evening dosing of valsartan.
Crikelair, N; Kandra, A; Palatini, P; Zappe, DH, 2015
)
0.42
" Initial dosage (Neb/Val 5/160 mg/d) was titrated up to 20/320 mg/d to achieve blood pressure (BP) goal (JNC7 criteria), with the addition of hydrochlorothiazide (up to 25 mg/d) if needed."( Long-term safety of nebivolol and valsartan combination therapy in patients with hypertension: an open-label, single-arm, multicenter study.
Finck, A; Giles, TD; Li, H; Neutel, JM; Punzi, H; Weiss, RJ, 2014
)
0.6
"A limited potential for clinically significant interactions between irbesartan and hydrochlorothiazide at the given doses were observed; therefore, no dosage adjustments were recommended for either drug when used together."( Modeling of the pharmacokinetic/pharmacodynamic interaction between irbesartan and hydrochlorothiazide in normotensive subjects.
Hedaya, MA; Helmy, SA, 2015
)
0.87
" The methods were successfully determined the three components in bulk powder, laboratory-prepared mixtures, and combined dosage forms."( Mean centering of ratio spectra and concentration augmented classical least squares in a comparative approach for quantitation of spectrally overlapped bands of antihypertensives in formulations.
Abdel Monem Hegazy, M; Fayez, YM, 2015
)
0.42
" Geometric mean ratios (90% CIs) for empagliflozin AUC over a uniform dosing interval and Cmax at steady state were 107."( Assessing pharmacokinetic interactions between the sodium glucose cotransporter 2 inhibitor empagliflozin and hydrochlorothiazide or torasemide in patients with type 2 diabetes mellitus: a randomized, open-label, crossover study.
Broedl, UC; Heise, T; Macha, S; Mattheus, M; Woerle, HJ, 2015
)
0.63
"A new rapid stability-indicating UPLC method for separation and determination of impurities in amlodipine besylate, valsartan and hydrochlorothiazide in their combined tablet dosage form was developed."( A new, rapid, stability-indicating UPLC method for separation and determination of impurities in amlodipine besylate, valsartan and hydrochlorothiazide in their combined tablet dosage form.
Coufal, P; Janečková, L; Jedlička, A; Vojta, J, 2015
)
0.83
" The ANCOVA showed that changes in patients' HRQoL was likely to have been influenced by patients' achievement of blood pressure control, the amount of concomitant medication and patients' last used dosage strength of antihypertensive."( Health-related quality of life impact of a triple combination of olmesartan medoxomil, amlodipine besylate and hydrochlorotiazide in subjects with hypertension.
Brazier, JE; Guest, JF; Haag, U; Marques da Silva, P; Soro, M, 2015
)
0.42
" Achieving blood pressure control, amount of concomitant medication and dosage strength of antihypertensive impacted on patients' HRQoL."( Health-related quality of life impact of a triple combination of olmesartan medoxomil, amlodipine besylate and hydrochlorotiazide in subjects with hypertension.
Brazier, JE; Guest, JF; Haag, U; Marques da Silva, P; Soro, M, 2015
)
0.42
"The primary purpose of this study was to process partially hydrolyzed PVOH grades (degree of hydroxylation (DH): 33-88%) via HME and to evaluate them as carrier for oral immediate release dosage forms in order to improve the release rate of poorly water soluble drugs (i."( Hot-melt extrusion of polyvinyl alcohol for oral immediate release applications.
De Beer, T; De Jaeghere, W; Remon, JP; Van Bocxlaer, J; Vervaet, C, 2015
)
0.42
" In vitro metoprolol tartrate release from the ethylcellulose core of the calendered tablets was prolonged in comparison with the sustained release of a multiparticulate dosage form, prepared manually by cutting co-extrudates into mini-matrices."( Calendering as a direct shaping tool for the continuous production of fixed-dose combination products via co-extrusion.
Bongaers, E; Lin, H; Remon, JP; Vervaet, C; Voorspoels, J; Vynckier, AK; Willart, JF; Zeitler, JA, 2015
)
0.42
"The significant increase in urine volume 24 h after treatment followed a dose-response pattern."( Evaluation of the diuretic effects of crude stem bark extraction of Zanthoxylum heitzii (Rutaceae) in Wistar rats.
Abakar, D; Dimo, T; Fokam, MA; Kakesse, M; Ntchapda, F; Pancha, OM, 2015
)
0.42
"We have used three dimensional (3D) extrusion printing to manufacture a multi-active solid dosage form or so called polypill."( 3D printing of five-in-one dose combination polypill with defined immediate and sustained release profiles.
Alexander, MR; Burley, JC; Khaled, SA; Roberts, CJ; Yang, J, 2015
)
0.42
" Specificity was investigated by analyzing the synthetic mixtures containing different ratios of the three studied drugs and their tablets dosage form."( Application and validation of superior spectrophotometric methods for simultaneous determination of ternary mixture used for hypertension management.
Lamie, NT; Mohamed, HM, 2016
)
0.43
" Two different three-way analysis methods, PARAFAC and 3W-PLS1, were successfully applied to the quantitative estimation of the solid dosage form containing HCT and OLM."( Three-way analysis of the UPLC-PDA dataset for the multicomponent quantitation of hydrochlorothiazide and olmesartan medoxomil in tablets by parallel factor analysis and three-way partial least squares.
Dinç, E; Ertekin, ZC, 2016
)
0.66
" Both drugs equally reduced SBP in the last 6 h of the dosing interval and homogeneously reduced SBP throughout the 24 h."( Zofenopril or irbesartan plus hydrochlorothiazide in elderly patients with isolated systolic hypertension untreated or uncontrolled by previous treatment: a double-blind, randomized study.
Arca, M; Berra, S; Bucci, M; Calabrò, P; Fulgheri, PL; Ghione, S; Modesti, PA; Omboni, S; Pirvu, O; Popescu, E; Portaluppi, F; Pozzilli, P; Taddei, S; Velican, VG; Villani, GQ; Vladoianu, M; Volpe, M, 2016
)
0.72
"Hypertensive patients who had not achieved their target blood pressure with at least 4 weeks of ARB therapy were randomly assigned to receive either a fixed-dose combination of losartan and HCTZ (losartan/HCTZ; n=110) or a combination of amlodipine and a typical ARB dosage (CCB/ARB; n=121) and followed for 24 weeks."( Effect of Diuretic or Calcium-Channel Blocker Plus Angiotensin-Receptor Blocker on Diastolic Function in Hypertensive Patients.
Ishii, K; Ito, H; Iwakura, K; Kihara, H; Toh, N; Watanabe, H; Yoshikawa, J, 2016
)
0.43
" Night-time dosing of thiazides may be particularly beneficial in patients with modest glucocorticoid excess."( Glucocorticoids Induce Nondipping Blood Pressure by Activating the Thiazide-Sensitive Cotransporter.
Al-Dujaili, EA; Bailey, MA; Dear, JW; Dhaun, N; Flatman, PW; Howarth, AR; Hunter, RW; Ivy, JR; Oosthuyzen, W; Peltz, TS; Webb, DJ, 2016
)
0.43
"Simultaneous spectrophotometric analysis of a multi-component dosage form of olmesartan, amlodipine and hydrochlorothiazide used for the treatment of hypertension has been carried out using various chemometric methods."( Simultaneous quantitative analysis of olmesartan, amlodipine and hydrochlorothiazide in their combined dosage form utilizing classical and alternating least squares based chemometric methods.
Abdelhameed, AS; Bakheit, AH; Darwish, HW, 2016
)
0.89
"A novel, simple and robust high-performance liquid chromatography (HPLC) method was developed and validated for simultaneous determination of xipamide (XIP), triamterene (TRI) and hydrochlorothiazide (HCT) in their bulk powders and dosage forms."( High performance liquid chromatography for simultaneous determination of xipamide, triamterene and hydrochlorothiazide in bulk drug samples and dosage forms.
Abd El-Hay, SS; Gouda, AA; Hashem, H, 2016
)
0.84
"Mini-tablets are increasingly gaining attention in solid dosage form design as multiple-unit systems combining different active compounds and providing a single or combined pattern of modified release for polypharmacy or combined treatments."( Mini-tablet combination for sustained release of clonidine hydrochloride and hydrochlorothiazide: Preparation and pharmacokinetics in beagle dogs.
Wang, Y; Xu, B; Zhu, H, 2016
)
0.66
"Four new spectrophotometric methods were developed, applied to resolve the overlapped spectra of a ternary mixture of [aliskiren hemifumarate (ALS)-amlodipine besylate (AM)-hydrochlorothiazide (HCT)] and to determine the three drugs in pure form and in combined dosage form."( Resolution of overlapped spectra for the determination of ternary mixture using different and modified spectrophotometric methods.
Ahmed, MS; El-Zaher, AA; Mahrouse, MA; Moussa, BA, 2016
)
0.63
" Although the pharmacology of ROMK channels is still being developed, channel inhibitors have been identified and shown to cause natriuresis and diuresis, in the absence of any significant kaliuresis, on acute oral dosing to rats or dogs."( The Renal Outer Medullary Potassium Channel Inhibitor, MK-7145, Lowers Blood Pressure, and Manifests Features of Bartter's Syndrome Type II Phenotype.
Alonso-Galicia, M; Corona, A; Felix, JP; Garcia, ML; Gill, C; Hampton, C; Kaczorowski, GJ; Kohler, M; Liu, J; Metzger, JM; Ormes, J; Owens, K; Pai, LY; Pasternak, A; Price, O; Priest, BT; Rasa, C; Roy, S; Shah, K; Sullivan, KA; Tang, H; Thomas-Fowlkes, B; Tong, V; Xiao, J; Zhou, X, 2016
)
0.43
"Three multivariate calibration spectrophotometric methods were developed for simultaneous estimation of Paracetamol (PARA), Enalapril maleate (ENM) and Hydrochlorothiazide (HCTZ) in tablet dosage form; namely multi-linear regression calibration (MLRC), trilinear regression calibration method (TLRC) and classical least square (CLS) method."( Development and validation of multivariate calibration methods for simultaneous estimation of Paracetamol, Enalapril maleate and hydrochlorothiazide in pharmaceutical dosage form.
Daharwal, SJ; Singh, VD, 2017
)
0.86
"A fast and selective capillary electrophoresis method has been developed for the simultaneous determination of the antihypertensive drugs captopril and hydrochlorothiazide and their related impurities in a combined dosage form."( Cyclodextrin- and solvent-modified micellar electrokinetic chromatography for the determination of captopril, hydrochlorothiazide and their impurities: A Quality by Design approach.
Brusotti, G; Caprini, C; Del Bubba, M; Furlanetto, S; Innocenti, M; Orlandini, S; Pasquini, B, 2016
)
0.84
" The initial dosage of valsartan 80 mg/day was titrated up to 320 mg/day to achieve the BP goal, with the addition of hydrochlorothiazide (HCTZ) in a fixed-dose combination (FDC), if needed."( The efficacy and safety of valsartan and combination of valsartan and hydrochlorothiazide in the treatment of patients with mild to moderate arterial hypertension - the VICTORY trial.
Accetto, R; Barbič-Žagar, B; Chazova, IY; Sirenko, Y; Vincelj, J; Widimsky, J, 2017
)
0.9
" However, their fluid nature limited the stability of the loaded drug and hindered the development of stable oral dosage form."( Self dispersing mixed micelles forming systems for enhanced dissolution and intestinal permeability of hydrochlorothiazide.
El Maghraby, GM; El-Gizawy, SA; Osman, MA; Sultan, AA, 2017
)
0.67
"To evaluate the effects of canrenone as add-on therapy in patients already treated with angiotensin-converting enzyme inhibitors (ACE-I) or angiotensin II receptor blockers (ARBs) and hydrochlorothiazide at the maximum dosage (25 mg/d)."( Efficacy and safety of two dosages of canrenone as add-on therapy in hypertensive patients taking ace-inhibitors or angiotensin II receptor blockers and hydrochlorothiazide at maximum dosage in a randomized clinical trial: The ESCAPE-IT trial.
Bestetti, A; D'Avino, M; Derosa, G; Felis, S; Gaudio, G; Guasti, L; Maffioli, P; Mugellini, A; Sala, C; Sarzani, R; Vanasia, M; Vulpis, V, 2017
)
0.84
" There was a clear dose-response effect (P < 0."( Hydrochlorothiazide use is strongly associated with risk of lip cancer.
Friedman, GD; Friis, S; Habel, LA; Hallas, J; Olesen, M; Pottegård, A; Svendsen, MT, 2017
)
1.9
" Furthermore, the developed procedure was adapted for studying the content uniformity test of some dosage forms containing the cited drug."( An innovative validated spectrofluorimetric method for determination of Lisinopril in presence of hydrochlorothiazide; application to content uniformity testing.
Badr El-Din, KM; Derayea, SM; Mohammed, FF, 2018
)
0.7
"Conventional immediate release dosage forms involve compressing the powder with a disintegrating agent that enables rapid disintegration and dissolution upon oral ingestion."( Channelled tablets: An innovative approach to accelerating drug release from 3D printed tablets.
Ahmed, W; Alhnan, MA; Arafat, B; Forbes, RT; Sadia, M, 2018
)
0.48
"Orodispersible films have been described as new beneficial dosage forms for special patient populations."( Orodispersible films: Product transfer from lab-scale to continuous manufacturing.
Breitkreutz, J; Thabet, Y, 2018
)
0.48
" However, to be considered as a viable processing option for solid oral dosage forms there is a need to understand all critical sources of variability which could affect this granulation technique."( Downstream processing from melt granulation towards tablets: In-depth analysis of a continuous twin-screw melt granulation process using polymeric binders.
De Beer, T; Grymonpré, W; Remon, JP; Vanhoorne, V; Verstraete, G; Vervaet, C, 2018
)
0.48
" Until now, there are only a few products available for the paediatric population due to the lack of age appropriate dosage forms or studies proving the efficacy and safety of these products."( Continuous manufacturing and analytical characterization of fixed-dose, multilayer orodispersible films.
Breitkreutz, J; Lunter, D; Thabet, Y, 2018
)
0.48
" AZL-M/CLD showed greater systolic BP reductions after initial dosing (P = ."( Long-term efficacy and tolerability of azilsartan medoxomil/chlorthalidone vs olmesartan medoxomil/hydrochlorothiazide in chronic kidney disease.
Bakris, GL; Hisada, M; Juhasz, A; Kupfer, S; Lloyd, E; Oparil, S; Zhao, L, 2018
)
0.7
" Consistency of cases and a dose-response relationship was also observed in this case series."( Hydrochlorothiazide and risk of hearing disorder: a case series.
Belai, N; Fitsum, Y; Gebrehiwet, S; Russom, M, 2018
)
1.92
" Since a single exposure to hydrochlorothiazide is not detectable in hair and based on the results of the patients on daily treatment, the concentration found in the athlete has been interpreted as corresponding to repeated exposures, where it was not possible to establish the dosage and the frequency."( First identification of a diuretic, hydrochlorothiazide, in hair: Application to a doping case and interpretation of the results.
Gheddar, L; Kintz, P; Raul, JS, 2019
)
1.08
" This dynamic dosing system maintained the advantages of FDCs while providing a superior flexibility of dosing range, hence offering an optimal clinical solution to hypertension therapy in a patient-centric healthcare service."( From 'fixed dose combinations' to 'a dynamic dose combiner': 3D printed bi-layer antihypertensive tablets.
Abbadi, I; Alhnan, MA; Aziz, D; Isreb, A; Isreb, M; Sadia, M; Selo, A; Timmins, P, 2018
)
0.48
" It was confirmed that the degradation product was formed by the reaction of amlodipine with formaldehyde originating from the excipients present in the dosage form."( Identification and structure elucidation of a new degradation impurity in the multi-component tablets of amlodipine besylate.
Břicháč, J; Douša, M; Gibala, P; Kalášek, S; Kalužíková, A; Štefko, M; Tkadlecová, M, 2019
)
0.51
" A higher bioavailability can reduce both the applied dosage and the side effects for the patient."( Preparation of submicron drug particles via spray drying from organic solvents.
Dobrowolski, A; Dräger-Gillessen, JF; Pieloth, D; Schaldach, G; Strob, R; Thommes, M; Wiggers, H, 2019
)
0.51
" Fused-filament fabrication (FFF) offers a platform for the personalization of drug dosage forms, but one of its chief shortcomings compared to other tablet production methods such as dry compression and wet granulation is relatively low throughput."( Mass-customization of oral tablets via the combination of 3D printing and injection molding.
Devine, DM; Doran, P; Fuenmayor, E; Gately, N; Lyons, JG; Major, I; McConville, C; O'Donnell, C, 2019
)
0.51
"The development of orodispersible mini-tablets (ODMTs) for paediatric use has gained importance within recent years as European authorities set up regulations for developing suitable and palatable dosage forms for paediatric patients."( New orodispersible mini-tablets for paediatric use - A comparison of isomalt with a mannitol based co-processed excipient.
Breitkreutz, J; Luhn, O; Lura, A; Suarez Gonzales, J, 2019
)
0.51
"High cumulative use of HCTZ may have a chemopreventive effect against the development of melanoma and NMSC with clear cumulative dose-response and duration-response relationships in South Korea."( Hydrochlorothiazide use and the risk of skin cancer in patients with hypertensive disorder: a nationwide retrospective cohort study from Korea.
Jue, MS; Lee, Y; Park, E, 2020
)
2
" Hydrochlorothiazide (HCTZ) is a recommended drug for the prevention of heart disease, but its long action (>4 h) dosage form is lacking in the commercial market and development of modified-release formulation may have industrial significance."( Employment of Quality by Design Approach via Response Surface Methodology to Optimize and Develop Modified-release Formulation of Hydrochlorothiazide.
Maheshwari, R; Paliwal, S; Sharma, S; Singhai, VD, 2021
)
1.74
" Once weekly oral dosing of nano-FDC of amlodipine, CNDT and hydrochlorothiazide provided adequate antihypertensive effect which was not statistically different from daily dosing of free drugs in dexamethasone-induced animal model."( Pharmacokinetic and pharmacodynamic evaluation of nano-fixed dose combination for hypertension.
Bhandari, RK; Bhatia, A; Kaur, N; Malhotra, S; Pandey, AK; Rather, IIG; Shafiq, N; Sharma, S, 2020
)
0.8
"Once weekly oral dosing of nano-FDC of amlodipine, CNDT and hydrochlorothiazide provided adequate antihypertensive effect and was not statistically different from daily dosing of free drugs in dexamethasone-induced animal model."( Pharmacokinetic and pharmacodynamic evaluation of nano-fixed dose combination for hypertension.
Bhandari, RK; Bhatia, A; Kaur, N; Malhotra, S; Pandey, AK; Rather, IIG; Shafiq, N; Sharma, S, 2020
)
0.8
"Orally disintegrating tablets (ODTs) manufactured by freeze-drying, also called oral lyophilizates, are a patient-centred dosage form."( Application of polyvinyl acetate in an innovative formulation strategy for lyophilized orally disintegrating tablets.
De Beer, T; Vanbillemont, B, 2020
)
0.56
" Dosing simulations were performed with a standardized 1mg/kg."( Pharmacokinetics of Hydrochlorothiazide in Children: A Potential Surrogate for Renal Secretion Maturation.
Al-Uzri, A; Boakye-Agyeman, F; Cohen-Wolkowiez, M; Commander, SJ; Harper, B; Hornik, CD; Hornik, CP; Melloni, C; Mendley, SR; Wu, H; Zimmerman, K, 2021
)
0.94
"08), with no evidence of duration- or dose-response relationships."( Use of Hydrochlorothiazide and Risk of Melanoma and Nonmelanoma Skin Cancer.
Azoulay, L; Nirantharakumar, K; Pottegård, A; Rouette, J; Yin, H, 2021
)
1.08
"Use of hydrochlorothiazide was associated with an increased risk of cSCC and with evidence of a duration- and dose-response relationship."( Use of Hydrochlorothiazide and Risk of Melanoma and Nonmelanoma Skin Cancer.
Azoulay, L; Nirantharakumar, K; Pottegård, A; Rouette, J; Yin, H, 2021
)
1.53
" The method was successfully used for quality control laboratories and the determination of these drugs combinations in pharmaceutical dosage forms."( Development and Validation of a UPLC-DAD Method for the Simultaneous Quantification of Eight Antihypertensive Drugs in the Pharmaceutical Matrix.
Abousalih, FZ; Azougagh, M; Benchekroun, YH; Bennani, I; Bouatia, M; El Karbane, M; Saffaj, T, 2021
)
0.62
"In 2018, the Pharmacological Risk Assessment Committee alerted to a potential relationship between accumulated hydrochlorothiazide dosage and the risk of non-melanoma skin cancer."( Hydrochlorothiazide use and risk of non-melanoma skin cancer in Spain: A case/non-case study.
Lecaros-Astorga, DA; Martin-Arias, LH; Molina-Guarneros, JA; Rodríguez-Jiménez, P; Sainz-Gil, M, 2021
)
2.28
" This work presents novel and green spectrophotometric methods for the concurrent analysis of Amlodipine (AML), Telmisartan (TEL), Hydrochlorothiazide (HCTZ), and Chlorthalidone (CLO) in their pharmaceutical dosage form."( Advanced eco-friendly UV spectrophotometric approach for resolving overlapped spectral signals of antihypertensive agents in their binary and tertiary pharmaceutical dosage form.
Attala, K; Elsonbaty, A, 2021
)
0.83
" A dose-response relationship was observed between cumulative doses of HCTZ and KC risk."( Use of hydrochlorothiazide and risk of skin cancer in a large nested case-control study in Spain.
Díaz, Y; Duarte-Salles, T; Huerta, C; León-Muñoz, LM; Llorente, A; Montero-Corominas, D; Pottegård, A; Puente, D, 2021
)
1.08
"In this European Mediterranean population, a high cumulative use of HCTZ was related to an increased risk of KC with a clear dose-response pattern."( Use of hydrochlorothiazide and risk of skin cancer in a large nested case-control study in Spain.
Díaz, Y; Duarte-Salles, T; Huerta, C; León-Muñoz, LM; Llorente, A; Montero-Corominas, D; Pottegård, A; Puente, D, 2021
)
1.08
" We did not find a dose-response relationship between HCTZ use and NMSC."( Is there a Link between Non Melanoma Skin Cancer and Hydrochlorothiazide?
Cione, E; De Sarro, G; Gallelli, L; Gerace, A; Guerra, A; Leuzzi, G; Longo, L; Luciani, F; Muraca, L; Natale, V; Scaramuzzino, A; Scuteri, A; Siniscalchi, A; Vasapollo, P; Vasta, G; Zampogna, S, 2022
)
0.97
" This demonstrates the suitability of the HME-paired FDM 3D-printing technique for improving solubility and developing on-demand patient-focused dosage forms for poorly soluble high-melting-point drug substances by utilizing a cocrystal approach."( Feasibility of high melting point hydrochlorothiazide processing via cocrystal formation by hot melt extrusion paired fused filament fabrication as a 3D-printed cocrystal tablet.
Alzahrani, A; Bandari, S; Kolimi, P; Mandati, P; Narala, S; Nyavanandi, D; Pradhan, A; Repka, MA, 2022
)
1
" Low-dose irbesartan and hydrochlorothiazide combined with levamlodipine at different times can effectively treat NDH, but bedtime dosing is more beneficial in reducing nocturnal blood pressure, reversing NDH, improving the circadian rhythm of blood pressure, left ventricular structure, regulating vascular endothelial function, increasing MMPs levels, and reducing TIMP levels."( Effect of administration of low-dose irbesartan and hydrochlorothiazide combined with levamlodipine at different times on the circadian rhythm of blood pressure and the levels of MMPs and TIMPs in non-dipper patients with grade 1 and 2 hypertension.
Chen, J; Dong, G; Ge, M; Liu, H; Luo, Y; Wang, J; Yan, P; Zhang, J, 2023
)
1.46
" Furthermore, dose-response data are also limited."( Hydrochlorothiazide and Prevention of Kidney-Stone Recurrence.
Bedino, G; Bonny, O; Bucher, C; Buchkremer, F; Cereghetti, GM; Christe, A; Del Giorno, R; Dhayat, NA; Ernandez, T; Faller, N; Fuster, DG; Gabutti, L; Grosse, P; Hüsler, C; Koneth, I; Mayr, M; Mohebbi, N; Odermatt, U; Pellegrini, L; Ritter, A; Roth, B; Roumet, M; Stoermann-Chopard, C; Tamò, L; Teta, D; Trelle, S; Venzin, RM; Vogt, B, 2023
)
2.35
" The main objective was to investigate the dose-response effect for the primary end point, a composite of symptomatic or radiologic recurrence of kidney stones."( Hydrochlorothiazide and Prevention of Kidney-Stone Recurrence.
Bedino, G; Bonny, O; Bucher, C; Buchkremer, F; Cereghetti, GM; Christe, A; Del Giorno, R; Dhayat, NA; Ernandez, T; Faller, N; Fuster, DG; Gabutti, L; Grosse, P; Hüsler, C; Koneth, I; Mayr, M; Mohebbi, N; Odermatt, U; Pellegrini, L; Ritter, A; Roth, B; Roumet, M; Stoermann-Chopard, C; Tamò, L; Teta, D; Trelle, S; Venzin, RM; Vogt, B, 2023
)
2.35
" The aim of this study was to investigate the association between hydrochlorothiazide use and incidence of skin cancer in a cohort of unselected Caucasian adults, taking dosing into account."( Chronic Use of Hydrochlorothiazide and Risk of Skin Cancer in Caucasian Adults: A PharmLines Initiative Inception Cohort Study.
Bos, J; De Bock, GH; De Vos, S; Greven, N; Haisma, MS; Hak, E; Horváth, B; Logendran, M; Rácz, E; van der Vegt, B, 2023
)
1.5
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
xenobioticA xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
diureticAn agent that promotes the excretion of urine through its effects on kidney function.
antihypertensive agentAny drug used in the treatment of acute or chronic vascular hypertension regardless of pharmacological mechanism.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (4)

ClassDescription
yohimban alkaloid
benzothiadiazineHeterocyclic compound of a ring with sulfur and two nitrogen atoms fused to a benzene ring. Members inhibit sodium-potassium-chloride symporters and are used as diuretics.
sulfonamideAn amide of a sulfonic acid RS(=O)2NR'2.
organochlorine compoundAn organochlorine compound is a compound containing at least one carbon-chlorine bond.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (2)

PathwayProteinsCompounds
Hydrochlorothiazide Action Pathway319
Nsp9 interactions (COVID-19 Disease Map)8330

Protein Targets (87)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency44.66840.003245.467312,589.2998AID2517
Chain A, TYROSYL-DNA PHOSPHODIESTERASEHomo sapiens (human)Potency49.48920.004023.8416100.0000AID485290
Chain A, Putative fructose-1,6-bisphosphate aldolaseGiardia intestinalisPotency12.89390.140911.194039.8107AID2451
Chain A, 2-oxoglutarate OxygenaseHomo sapiens (human)Potency19.95260.177814.390939.8107AID2147
TDP1 proteinHomo sapiens (human)Potency31.67680.000811.382244.6684AID686978; AID686979
Microtubule-associated protein tauHomo sapiens (human)Potency28.18380.180013.557439.8107AID1460
EWS/FLI fusion proteinHomo sapiens (human)Potency2.64380.001310.157742.8575AID1259252; AID1259253; AID1259255; AID1259256
cytochrome P450 3A4 isoform 1Homo sapiens (human)Potency3.16230.031610.279239.8107AID884; AID885
DNA dC->dU-editing enzyme APOBEC-3G isoform 1Homo sapiens (human)Potency5.95690.058010.694926.6086AID588379
Gamma-aminobutyric acid receptor subunit piRattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Polyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)Potency7.94330.316212.765731.6228AID881
Gamma-aminobutyric acid receptor subunit beta-1Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit deltaRattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-2Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-5Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-3Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-1Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-2Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-4Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-3Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-6Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Histamine H2 receptorCavia porcellus (domestic guinea pig)Potency7.94330.00638.235039.8107AID881
Gamma-aminobutyric acid receptor subunit alpha-1Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit beta-3Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit beta-2Rattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
GABA theta subunitRattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit epsilonRattus norvegicus (Norway rat)Potency3.16231.000012.224831.6228AID885
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency21.67940.003245.467312,589.2998AID1705; AID2517
acetylcholinesteraseHomo sapiens (human)Potency70.45940.002541.796015,848.9004AID1347395
RAR-related orphan receptor gammaMus musculus (house mouse)Potency30.17110.006038.004119,952.5996AID1159521
ATAD5 protein, partialHomo sapiens (human)Potency32.62940.004110.890331.5287AID493107
GLI family zinc finger 3Homo sapiens (human)Potency21.17790.000714.592883.7951AID1259369
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency13.33320.001022.650876.6163AID1224839
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency50.11870.000214.376460.0339AID588532
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency42.61780.003041.611522,387.1992AID1159552
retinoid X nuclear receptor alphaHomo sapiens (human)Potency32.61960.000817.505159.3239AID1159527; AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency1.51210.001530.607315,848.9004AID1224841
estrogen nuclear receptor alphaHomo sapiens (human)Potency35.12900.000229.305416,493.5996AID1259244; AID743075
GVesicular stomatitis virusPotency17.37680.01238.964839.8107AID1645842
arylsulfatase AHomo sapiens (human)Potency0.15101.069113.955137.9330AID720538
euchromatic histone-lysine N-methyltransferase 2Homo sapiens (human)Potency0.31620.035520.977089.1251AID504332
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency60.74090.057821.109761.2679AID1159526
peripheral myelin protein 22 isoform 1Homo sapiens (human)Potency95.283423.934123.934123.9341AID1967
cytochrome P450 2C9 precursorHomo sapiens (human)Potency19.78310.00636.904339.8107AID883
chromobox protein homolog 1Homo sapiens (human)Potency64.46790.006026.168889.1251AID488953; AID540317
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.28180.010039.53711,122.0200AID1479
gemininHomo sapiens (human)Potency0.05170.004611.374133.4983AID624296
survival motor neuron protein isoform dHomo sapiens (human)Potency1.25890.125912.234435.4813AID1458
lamin isoform A-delta10Homo sapiens (human)Potency0.00260.891312.067628.1838AID1487
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency67.54470.001557.789015,848.9004AID1259244
Interferon betaHomo sapiens (human)Potency17.37680.00339.158239.8107AID1645842
HLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)Potency17.37680.01238.964839.8107AID1645842
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency67.54470.001551.739315,848.9004AID1259244
Histamine H2 receptorCavia porcellus (domestic guinea pig)Potency19.78310.00638.235039.8107AID883
Spike glycoproteinSevere acute respiratory syndrome-related coronavirusPotency6.30960.009610.525035.4813AID1479145
Guanine nucleotide-binding protein GHomo sapiens (human)Potency10.00001.995325.532750.1187AID624288
Inositol hexakisphosphate kinase 1Homo sapiens (human)Potency17.37680.01238.964839.8107AID1645842
cytochrome P450 2C9, partialHomo sapiens (human)Potency17.37680.01238.964839.8107AID1645842
ATP-dependent phosphofructokinaseTrypanosoma brucei brucei TREU927Potency8.49210.060110.745337.9330AID485368
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Carbonic anhydrase Astrosclera willeyanaKi0.39400.03201.51729.6000AID644379
Carbonic anhydrase Sulfurihydrogenibium sp. YO3AOP1Ki0.00720.00450.16240.8760AID1268964
ATP-binding cassette sub-family C member 3Homo sapiens (human)IC50 (µMol)133.00000.63154.45319.3000AID1473740
Multidrug resistance-associated protein 4Homo sapiens (human)IC50 (µMol)133.00000.20005.677410.0000AID1473741
Solute carrier family 22 member 6Rattus norvegicus (Norway rat)Ki150.00001.60005.744010.0000AID681388
Carbonic anhydrase 12Homo sapiens (human)Ki18.60420.00021.10439.9000AID1798598
Bile salt export pumpHomo sapiens (human)IC50 (µMol)133.00000.11007.190310.0000AID1473738
Carbonic anhydrase 1Homo sapiens (human)Ki7.63850.00001.372610.0000AID1142833; AID1188134; AID1190063; AID1194024; AID1195369; AID1262263; AID1268962; AID1275913; AID1287517; AID1434427; AID1453412; AID1628036; AID1798598; AID587130; AID612725; AID644380; AID711214; AID725955; AID743515
Carbonic anhydrase 2Homo sapiens (human)IC50 (µMol)121,313,329,153.83180.00021.10608.3000AID1796991; AID48105
Carbonic anhydrase 2Homo sapiens (human)Ki6.94970.00000.72369.9200AID1061069; AID1142834; AID1188135; AID1190064; AID1194025; AID1195370; AID1240217; AID1262264; AID1268963; AID1275912; AID1278409; AID1287518; AID1434428; AID1453413; AID1628037; AID1798598; AID587131; AID612726; AID644381; AID711213; AID725956; AID743514
Carbonic anhydrase 3Homo sapiens (human)Ki18.60420.00022.010210.0000AID1798598
Cytochrome P450 2C9 Homo sapiens (human)IC50 (µMol)50.00000.00002.800510.0000AID1210069
Carbonic anhydrase 4Homo sapiens (human)Ki18.60420.00021.97209.9200AID1798598
Carbonic anhydrase 6Homo sapiens (human)Ki18.60420.00011.47109.9200AID1798598
Delta-type opioid receptorMus musculus (house mouse)Ki0.30900.00000.53939.4000AID1188134; AID1188135
Delta-type opioid receptorRattus norvegicus (Norway rat)Ki0.29000.00000.60689.2330AID1188135
Mu-type opioid receptorRattus norvegicus (Norway rat)Ki0.32800.00000.38458.6000AID1188134
Carbonic anhydrase 5A, mitochondrialHomo sapiens (human)Ki18.60420.00001.27259.9000AID1798598
Carbonic anhydrase 7Homo sapiens (human)Ki18.60420.00021.37379.9000AID1798598
Cytochrome P450 2J2Homo sapiens (human)IC50 (µMol)50.00000.01202.53129.4700AID1210069
Mu-type opioid receptorCavia porcellus (domestic guinea pig)Ki0.29000.00000.27869.0000AID1188135
Carbonic anhydrase 9Homo sapiens (human)Ki18.60420.00010.78749.9000AID1798598
Carbonic anhydrase, alpha family Hydrogenovibrio crunogenus XCL-2Ki0.29600.00250.32341.1000AID1268965
Carbonic anhydrase Anopheles gambiae (African malaria mosquito)Ki0.03150.00980.51174.3600AID1195371
Delta carbonic anhydraseConticribra weissflogiiKi4.27000.04960.99789.2000AID1061066
Canalicular multispecific organic anion transporter 1Homo sapiens (human)IC50 (µMol)133.00002.41006.343310.0000AID1473739
Carbonic anhydrase 13Mus musculus (house mouse)Ki18.60420.00021.39749.9000AID1798598
Carbonic anhydrase 14Homo sapiens (human)Ki18.60420.00021.50999.9000AID1798598
Carbonic anhydrase 5B, mitochondrialHomo sapiens (human)Ki18.60420.00001.34129.9700AID1798598
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Hsf1 proteinMus musculus (house mouse)EC50 (µMol)195.00000.160024.4900236.5000AID2382
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (152)

Processvia Protein(s)Taxonomy
lipid metabolic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
phospholipid metabolic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
apoptotic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
negative regulation of cell population proliferationPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
positive regulation of macrophage derived foam cell differentiationPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
arachidonic acid metabolic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
negative regulation of cell migrationPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
prostate gland developmentPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
regulation of epithelial cell differentiationPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
positive regulation of chemokine productionPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
positive regulation of peroxisome proliferator activated receptor signaling pathwayPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
positive regulation of keratinocyte differentiationPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
negative regulation of cell cyclePolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
negative regulation of growthPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
hepoxilin biosynthetic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
endocannabinoid signaling pathwayPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
cannabinoid biosynthetic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
lipoxin A4 biosynthetic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
linoleic acid metabolic processPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
lipid oxidationPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
lipoxygenase pathwayPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
xenobiotic metabolic processATP-binding cassette sub-family C member 3Homo sapiens (human)
xenobiotic transmembrane transportATP-binding cassette sub-family C member 3Homo sapiens (human)
bile acid and bile salt transportATP-binding cassette sub-family C member 3Homo sapiens (human)
glucuronoside transportATP-binding cassette sub-family C member 3Homo sapiens (human)
xenobiotic transportATP-binding cassette sub-family C member 3Homo sapiens (human)
transmembrane transportATP-binding cassette sub-family C member 3Homo sapiens (human)
leukotriene transportATP-binding cassette sub-family C member 3Homo sapiens (human)
monoatomic anion transmembrane transportATP-binding cassette sub-family C member 3Homo sapiens (human)
transport across blood-brain barrierATP-binding cassette sub-family C member 3Homo sapiens (human)
prostaglandin secretionMultidrug resistance-associated protein 4Homo sapiens (human)
cilium assemblyMultidrug resistance-associated protein 4Homo sapiens (human)
platelet degranulationMultidrug resistance-associated protein 4Homo sapiens (human)
xenobiotic metabolic processMultidrug resistance-associated protein 4Homo sapiens (human)
xenobiotic transmembrane transportMultidrug resistance-associated protein 4Homo sapiens (human)
bile acid and bile salt transportMultidrug resistance-associated protein 4Homo sapiens (human)
prostaglandin transportMultidrug resistance-associated protein 4Homo sapiens (human)
urate transportMultidrug resistance-associated protein 4Homo sapiens (human)
glutathione transmembrane transportMultidrug resistance-associated protein 4Homo sapiens (human)
transmembrane transportMultidrug resistance-associated protein 4Homo sapiens (human)
cAMP transportMultidrug resistance-associated protein 4Homo sapiens (human)
leukotriene transportMultidrug resistance-associated protein 4Homo sapiens (human)
monoatomic anion transmembrane transportMultidrug resistance-associated protein 4Homo sapiens (human)
export across plasma membraneMultidrug resistance-associated protein 4Homo sapiens (human)
transport across blood-brain barrierMultidrug resistance-associated protein 4Homo sapiens (human)
guanine nucleotide transmembrane transportMultidrug resistance-associated protein 4Homo sapiens (human)
estrous cycleCarbonic anhydrase 12Homo sapiens (human)
chloride ion homeostasisCarbonic anhydrase 12Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 12Homo sapiens (human)
fatty acid metabolic processBile salt export pumpHomo sapiens (human)
bile acid biosynthetic processBile salt export pumpHomo sapiens (human)
xenobiotic metabolic processBile salt export pumpHomo sapiens (human)
xenobiotic transmembrane transportBile salt export pumpHomo sapiens (human)
response to oxidative stressBile salt export pumpHomo sapiens (human)
bile acid metabolic processBile salt export pumpHomo sapiens (human)
response to organic cyclic compoundBile salt export pumpHomo sapiens (human)
bile acid and bile salt transportBile salt export pumpHomo sapiens (human)
canalicular bile acid transportBile salt export pumpHomo sapiens (human)
protein ubiquitinationBile salt export pumpHomo sapiens (human)
regulation of fatty acid beta-oxidationBile salt export pumpHomo sapiens (human)
carbohydrate transmembrane transportBile salt export pumpHomo sapiens (human)
bile acid signaling pathwayBile salt export pumpHomo sapiens (human)
cholesterol homeostasisBile salt export pumpHomo sapiens (human)
response to estrogenBile salt export pumpHomo sapiens (human)
response to ethanolBile salt export pumpHomo sapiens (human)
xenobiotic export from cellBile salt export pumpHomo sapiens (human)
lipid homeostasisBile salt export pumpHomo sapiens (human)
phospholipid homeostasisBile salt export pumpHomo sapiens (human)
positive regulation of bile acid secretionBile salt export pumpHomo sapiens (human)
regulation of bile acid metabolic processBile salt export pumpHomo sapiens (human)
transmembrane transportBile salt export pumpHomo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 1Homo sapiens (human)
morphogenesis of an epitheliumCarbonic anhydrase 2Homo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 2Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 2Homo sapiens (human)
angiotensin-activated signaling pathwayCarbonic anhydrase 2Homo sapiens (human)
regulation of monoatomic anion transportCarbonic anhydrase 2Homo sapiens (human)
secretionCarbonic anhydrase 2Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 2Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 2Homo sapiens (human)
positive regulation of dipeptide transmembrane transportCarbonic anhydrase 2Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 2Homo sapiens (human)
carbon dioxide transportCarbonic anhydrase 2Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 2Homo sapiens (human)
cell surface receptor signaling pathway via JAK-STATInterferon betaHomo sapiens (human)
response to exogenous dsRNAInterferon betaHomo sapiens (human)
B cell activation involved in immune responseInterferon betaHomo sapiens (human)
cell surface receptor signaling pathwayInterferon betaHomo sapiens (human)
cell surface receptor signaling pathway via JAK-STATInterferon betaHomo sapiens (human)
response to virusInterferon betaHomo sapiens (human)
positive regulation of autophagyInterferon betaHomo sapiens (human)
cytokine-mediated signaling pathwayInterferon betaHomo sapiens (human)
natural killer cell activationInterferon betaHomo sapiens (human)
positive regulation of peptidyl-serine phosphorylation of STAT proteinInterferon betaHomo sapiens (human)
cellular response to interferon-betaInterferon betaHomo sapiens (human)
B cell proliferationInterferon betaHomo sapiens (human)
negative regulation of viral genome replicationInterferon betaHomo sapiens (human)
innate immune responseInterferon betaHomo sapiens (human)
positive regulation of innate immune responseInterferon betaHomo sapiens (human)
regulation of MHC class I biosynthetic processInterferon betaHomo sapiens (human)
negative regulation of T cell differentiationInterferon betaHomo sapiens (human)
positive regulation of transcription by RNA polymerase IIInterferon betaHomo sapiens (human)
defense response to virusInterferon betaHomo sapiens (human)
type I interferon-mediated signaling pathwayInterferon betaHomo sapiens (human)
neuron cellular homeostasisInterferon betaHomo sapiens (human)
cellular response to exogenous dsRNAInterferon betaHomo sapiens (human)
cellular response to virusInterferon betaHomo sapiens (human)
negative regulation of Lewy body formationInterferon betaHomo sapiens (human)
negative regulation of T-helper 2 cell cytokine productionInterferon betaHomo sapiens (human)
positive regulation of apoptotic signaling pathwayInterferon betaHomo sapiens (human)
response to exogenous dsRNAInterferon betaHomo sapiens (human)
B cell differentiationInterferon betaHomo sapiens (human)
natural killer cell activation involved in immune responseInterferon betaHomo sapiens (human)
adaptive immune responseInterferon betaHomo sapiens (human)
T cell activation involved in immune responseInterferon betaHomo sapiens (human)
humoral immune responseInterferon betaHomo sapiens (human)
positive regulation of T cell mediated cytotoxicityHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
adaptive immune responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independentHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of T cell anergyHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
defense responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
immune responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
detection of bacteriumHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of interleukin-12 productionHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of interleukin-6 productionHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
protection from natural killer cell mediated cytotoxicityHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
innate immune responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of dendritic cell differentiationHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
antigen processing and presentation of endogenous peptide antigen via MHC class IbHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
cellular response to starvationAlbuminHomo sapiens (human)
negative regulation of mitochondrial depolarizationAlbuminHomo sapiens (human)
cellular response to calcium ion starvationAlbuminHomo sapiens (human)
cellular oxidant detoxificationAlbuminHomo sapiens (human)
transportAlbuminHomo sapiens (human)
response to bacteriumCarbonic anhydrase 3Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 3Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 2C9 Homo sapiens (human)
steroid metabolic processCytochrome P450 2C9 Homo sapiens (human)
cholesterol metabolic processCytochrome P450 2C9 Homo sapiens (human)
estrogen metabolic processCytochrome P450 2C9 Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 2C9 Homo sapiens (human)
epoxygenase P450 pathwayCytochrome P450 2C9 Homo sapiens (human)
urea metabolic processCytochrome P450 2C9 Homo sapiens (human)
monocarboxylic acid metabolic processCytochrome P450 2C9 Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 2C9 Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 2C9 Homo sapiens (human)
amide metabolic processCytochrome P450 2C9 Homo sapiens (human)
icosanoid biosynthetic processCytochrome P450 2C9 Homo sapiens (human)
oxidative demethylationCytochrome P450 2C9 Homo sapiens (human)
omega-hydroxylase P450 pathwayCytochrome P450 2C9 Homo sapiens (human)
bicarbonate transportCarbonic anhydrase 4Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 4Homo sapiens (human)
detection of chemical stimulus involved in sensory perception of bitter tasteCarbonic anhydrase 6Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 6Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
positive regulation of synaptic transmission, GABAergicCarbonic anhydrase 7Homo sapiens (human)
positive regulation of cellular pH reductionCarbonic anhydrase 7Homo sapiens (human)
neuron cellular homeostasisCarbonic anhydrase 7Homo sapiens (human)
regulation of chloride transportCarbonic anhydrase 7Homo sapiens (human)
regulation of intracellular pHCarbonic anhydrase 7Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 7Homo sapiens (human)
fatty acid metabolic processCytochrome P450 2J2Homo sapiens (human)
icosanoid metabolic processCytochrome P450 2J2Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 2J2Homo sapiens (human)
regulation of heart contractionCytochrome P450 2J2Homo sapiens (human)
epoxygenase P450 pathwayCytochrome P450 2J2Homo sapiens (human)
linoleic acid metabolic processCytochrome P450 2J2Homo sapiens (human)
organic acid metabolic processCytochrome P450 2J2Homo sapiens (human)
negative regulation of inflammatory response to antigenic stimulusGuanine nucleotide-binding protein GHomo sapiens (human)
renal water homeostasisGuanine nucleotide-binding protein GHomo sapiens (human)
G protein-coupled receptor signaling pathwayGuanine nucleotide-binding protein GHomo sapiens (human)
regulation of insulin secretionGuanine nucleotide-binding protein GHomo sapiens (human)
cellular response to glucagon stimulusGuanine nucleotide-binding protein GHomo sapiens (human)
response to hypoxiaCarbonic anhydrase 9Homo sapiens (human)
morphogenesis of an epitheliumCarbonic anhydrase 9Homo sapiens (human)
response to xenobiotic stimulusCarbonic anhydrase 9Homo sapiens (human)
response to testosteroneCarbonic anhydrase 9Homo sapiens (human)
secretionCarbonic anhydrase 9Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 9Homo sapiens (human)
inositol phosphate metabolic processInositol hexakisphosphate kinase 1Homo sapiens (human)
phosphatidylinositol phosphate biosynthetic processInositol hexakisphosphate kinase 1Homo sapiens (human)
negative regulation of cold-induced thermogenesisInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol phosphate biosynthetic processInositol hexakisphosphate kinase 1Homo sapiens (human)
xenobiotic metabolic processCanalicular multispecific organic anion transporter 1Homo sapiens (human)
xenobiotic transmembrane transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
negative regulation of gene expressionCanalicular multispecific organic anion transporter 1Homo sapiens (human)
bile acid and bile salt transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
bilirubin transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
heme catabolic processCanalicular multispecific organic anion transporter 1Homo sapiens (human)
xenobiotic export from cellCanalicular multispecific organic anion transporter 1Homo sapiens (human)
transmembrane transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
transepithelial transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
leukotriene transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
monoatomic anion transmembrane transportCanalicular multispecific organic anion transporter 1Homo sapiens (human)
transport across blood-brain barrierCanalicular multispecific organic anion transporter 1Homo sapiens (human)
xenobiotic transport across blood-brain barrierCanalicular multispecific organic anion transporter 1Homo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 14Homo sapiens (human)
response to bacteriumCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
one-carbon metabolic processCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (83)

Processvia Protein(s)Taxonomy
iron ion bindingPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
calcium ion bindingPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
protein bindingPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
lipid bindingPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
linoleate 13S-lipoxygenase activityPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
arachidonate 8(S)-lipoxygenase activityPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
arachidonate 15-lipoxygenase activityPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
linoleate 9S-lipoxygenase activityPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
ATP bindingATP-binding cassette sub-family C member 3Homo sapiens (human)
ABC-type xenobiotic transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
glucuronoside transmembrane transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
ABC-type glutathione S-conjugate transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
ABC-type bile acid transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
ATP hydrolysis activityATP-binding cassette sub-family C member 3Homo sapiens (human)
ATPase-coupled transmembrane transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
xenobiotic transmembrane transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
ATPase-coupled inorganic anion transmembrane transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
icosanoid transmembrane transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
ABC-type transporter activityATP-binding cassette sub-family C member 3Homo sapiens (human)
guanine nucleotide transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
protein bindingMultidrug resistance-associated protein 4Homo sapiens (human)
ATP bindingMultidrug resistance-associated protein 4Homo sapiens (human)
ABC-type xenobiotic transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
prostaglandin transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
urate transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
purine nucleotide transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
ABC-type glutathione S-conjugate transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
ABC-type bile acid transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
efflux transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
15-hydroxyprostaglandin dehydrogenase (NAD+) activityMultidrug resistance-associated protein 4Homo sapiens (human)
ATP hydrolysis activityMultidrug resistance-associated protein 4Homo sapiens (human)
glutathione transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
ATPase-coupled transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
xenobiotic transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
ATPase-coupled inorganic anion transmembrane transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
ABC-type transporter activityMultidrug resistance-associated protein 4Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 12Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 12Homo sapiens (human)
protein bindingBile salt export pumpHomo sapiens (human)
ATP bindingBile salt export pumpHomo sapiens (human)
ABC-type xenobiotic transporter activityBile salt export pumpHomo sapiens (human)
bile acid transmembrane transporter activityBile salt export pumpHomo sapiens (human)
canalicular bile acid transmembrane transporter activityBile salt export pumpHomo sapiens (human)
carbohydrate transmembrane transporter activityBile salt export pumpHomo sapiens (human)
ABC-type bile acid transporter activityBile salt export pumpHomo sapiens (human)
ATP hydrolysis activityBile salt export pumpHomo sapiens (human)
arylesterase activityCarbonic anhydrase 1Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 1Homo sapiens (human)
protein bindingCarbonic anhydrase 1Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 1Homo sapiens (human)
hydro-lyase activityCarbonic anhydrase 1Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 1Homo sapiens (human)
arylesterase activityCarbonic anhydrase 2Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 2Homo sapiens (human)
protein bindingCarbonic anhydrase 2Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 2Homo sapiens (human)
cyanamide hydratase activityCarbonic anhydrase 2Homo sapiens (human)
cytokine activityInterferon betaHomo sapiens (human)
cytokine receptor bindingInterferon betaHomo sapiens (human)
type I interferon receptor bindingInterferon betaHomo sapiens (human)
protein bindingInterferon betaHomo sapiens (human)
chloramphenicol O-acetyltransferase activityInterferon betaHomo sapiens (human)
TAP bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
signaling receptor bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
protein bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
peptide antigen bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
TAP bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
protein-folding chaperone bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
oxygen bindingAlbuminHomo sapiens (human)
DNA bindingAlbuminHomo sapiens (human)
fatty acid bindingAlbuminHomo sapiens (human)
copper ion bindingAlbuminHomo sapiens (human)
protein bindingAlbuminHomo sapiens (human)
toxic substance bindingAlbuminHomo sapiens (human)
antioxidant activityAlbuminHomo sapiens (human)
pyridoxal phosphate bindingAlbuminHomo sapiens (human)
identical protein bindingAlbuminHomo sapiens (human)
protein-folding chaperone bindingAlbuminHomo sapiens (human)
exogenous protein bindingAlbuminHomo sapiens (human)
enterobactin bindingAlbuminHomo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 3Homo sapiens (human)
protein bindingCarbonic anhydrase 3Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 3Homo sapiens (human)
nickel cation bindingCarbonic anhydrase 3Homo sapiens (human)
monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
iron ion bindingCytochrome P450 2C9 Homo sapiens (human)
arachidonic acid epoxygenase activityCytochrome P450 2C9 Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 2C9 Homo sapiens (human)
arachidonic acid 14,15-epoxygenase activityCytochrome P450 2C9 Homo sapiens (human)
arachidonic acid 11,12-epoxygenase activityCytochrome P450 2C9 Homo sapiens (human)
oxidoreductase activityCytochrome P450 2C9 Homo sapiens (human)
(S)-limonene 6-monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
(S)-limonene 7-monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
caffeine oxidase activityCytochrome P450 2C9 Homo sapiens (human)
(R)-limonene 6-monooxygenase activityCytochrome P450 2C9 Homo sapiens (human)
aromatase activityCytochrome P450 2C9 Homo sapiens (human)
heme bindingCytochrome P450 2C9 Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 2C9 Homo sapiens (human)
protein bindingCarbonic anhydrase 4Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 4Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 4Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 6Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 6Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 7Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 7Homo sapiens (human)
monooxygenase activityCytochrome P450 2J2Homo sapiens (human)
iron ion bindingCytochrome P450 2J2Homo sapiens (human)
arachidonic acid epoxygenase activityCytochrome P450 2J2Homo sapiens (human)
arachidonic acid 14,15-epoxygenase activityCytochrome P450 2J2Homo sapiens (human)
arachidonic acid 11,12-epoxygenase activityCytochrome P450 2J2Homo sapiens (human)
isomerase activityCytochrome P450 2J2Homo sapiens (human)
linoleic acid epoxygenase activityCytochrome P450 2J2Homo sapiens (human)
hydroperoxy icosatetraenoate isomerase activityCytochrome P450 2J2Homo sapiens (human)
arachidonic acid 5,6-epoxygenase activityCytochrome P450 2J2Homo sapiens (human)
heme bindingCytochrome P450 2J2Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 2J2Homo sapiens (human)
G protein activityGuanine nucleotide-binding protein GHomo sapiens (human)
adenylate cyclase activator activityGuanine nucleotide-binding protein GHomo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 9Homo sapiens (human)
protein bindingCarbonic anhydrase 9Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 9Homo sapiens (human)
molecular function activator activityCarbonic anhydrase 9Homo sapiens (human)
inositol-1,3,4,5,6-pentakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol heptakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate 5-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
protein bindingInositol hexakisphosphate kinase 1Homo sapiens (human)
ATP bindingInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate 1-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate 3-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol 5-diphosphate pentakisphosphate 5-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol diphosphate tetrakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
protein bindingCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ATP bindingCanalicular multispecific organic anion transporter 1Homo sapiens (human)
organic anion transmembrane transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ABC-type xenobiotic transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
bilirubin transmembrane transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ABC-type glutathione S-conjugate transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ATP hydrolysis activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ATPase-coupled transmembrane transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
xenobiotic transmembrane transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ATPase-coupled inorganic anion transmembrane transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
ABC-type transporter activityCanalicular multispecific organic anion transporter 1Homo sapiens (human)
zinc ion bindingCarbonic anhydrase 14Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 14Homo sapiens (human)
carbonate dehydratase activityCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
zinc ion bindingCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (53)

Processvia Protein(s)Taxonomy
nucleusPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
cytosolPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
cytoskeletonPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
plasma membranePolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
adherens junctionPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
focal adhesionPolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
membranePolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
extracellular exosomePolyunsaturated fatty acid lipoxygenase ALOX15BHomo sapiens (human)
plasma membraneGamma-aminobutyric acid receptor subunit gamma-2Rattus norvegicus (Norway rat)
plasma membraneGamma-aminobutyric acid receptor subunit alpha-1Rattus norvegicus (Norway rat)
plasma membraneGamma-aminobutyric acid receptor subunit beta-2Rattus norvegicus (Norway rat)
plasma membraneATP-binding cassette sub-family C member 3Homo sapiens (human)
basal plasma membraneATP-binding cassette sub-family C member 3Homo sapiens (human)
basolateral plasma membraneATP-binding cassette sub-family C member 3Homo sapiens (human)
membraneATP-binding cassette sub-family C member 3Homo sapiens (human)
nucleolusMultidrug resistance-associated protein 4Homo sapiens (human)
Golgi apparatusMultidrug resistance-associated protein 4Homo sapiens (human)
plasma membraneMultidrug resistance-associated protein 4Homo sapiens (human)
membraneMultidrug resistance-associated protein 4Homo sapiens (human)
basolateral plasma membraneMultidrug resistance-associated protein 4Homo sapiens (human)
apical plasma membraneMultidrug resistance-associated protein 4Homo sapiens (human)
platelet dense granule membraneMultidrug resistance-associated protein 4Homo sapiens (human)
external side of apical plasma membraneMultidrug resistance-associated protein 4Homo sapiens (human)
plasma membraneMultidrug resistance-associated protein 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 12Homo sapiens (human)
membraneCarbonic anhydrase 12Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 12Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 12Homo sapiens (human)
plasma membraneCarbonic anhydrase 12Homo sapiens (human)
basolateral plasma membraneBile salt export pumpHomo sapiens (human)
Golgi membraneBile salt export pumpHomo sapiens (human)
endosomeBile salt export pumpHomo sapiens (human)
plasma membraneBile salt export pumpHomo sapiens (human)
cell surfaceBile salt export pumpHomo sapiens (human)
apical plasma membraneBile salt export pumpHomo sapiens (human)
intercellular canaliculusBile salt export pumpHomo sapiens (human)
intracellular canaliculusBile salt export pumpHomo sapiens (human)
recycling endosomeBile salt export pumpHomo sapiens (human)
recycling endosome membraneBile salt export pumpHomo sapiens (human)
extracellular exosomeBile salt export pumpHomo sapiens (human)
membraneBile salt export pumpHomo sapiens (human)
cytosolCarbonic anhydrase 1Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 1Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
cytosolCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
myelin sheathCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 2Homo sapiens (human)
cytoplasmCarbonic anhydrase 2Homo sapiens (human)
plasma membraneCarbonic anhydrase 2Homo sapiens (human)
apical part of cellCarbonic anhydrase 2Homo sapiens (human)
extracellular spaceInterferon betaHomo sapiens (human)
extracellular regionInterferon betaHomo sapiens (human)
Golgi membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
endoplasmic reticulumHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
Golgi apparatusHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
plasma membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
cell surfaceHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
ER to Golgi transport vesicle membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
secretory granule membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
phagocytic vesicle membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
early endosome membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
recycling endosome membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
extracellular exosomeHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
lumenal side of endoplasmic reticulum membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
MHC class I protein complexHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
extracellular spaceHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
external side of plasma membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
extracellular regionAlbuminHomo sapiens (human)
extracellular spaceAlbuminHomo sapiens (human)
nucleusAlbuminHomo sapiens (human)
endoplasmic reticulumAlbuminHomo sapiens (human)
endoplasmic reticulum lumenAlbuminHomo sapiens (human)
Golgi apparatusAlbuminHomo sapiens (human)
platelet alpha granule lumenAlbuminHomo sapiens (human)
extracellular exosomeAlbuminHomo sapiens (human)
blood microparticleAlbuminHomo sapiens (human)
protein-containing complexAlbuminHomo sapiens (human)
cytoplasmAlbuminHomo sapiens (human)
cytosolCarbonic anhydrase 3Homo sapiens (human)
cytosolCarbonic anhydrase 3Homo sapiens (human)
cytoplasmCarbonic anhydrase 3Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 2C9 Homo sapiens (human)
plasma membraneCytochrome P450 2C9 Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C9 Homo sapiens (human)
cytoplasmCytochrome P450 2C9 Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C9 Homo sapiens (human)
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
basolateral plasma membraneCarbonic anhydrase 4Homo sapiens (human)
rough endoplasmic reticulumCarbonic anhydrase 4Homo sapiens (human)
endoplasmic reticulum-Golgi intermediate compartmentCarbonic anhydrase 4Homo sapiens (human)
Golgi apparatusCarbonic anhydrase 4Homo sapiens (human)
trans-Golgi networkCarbonic anhydrase 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 4Homo sapiens (human)
external side of plasma membraneCarbonic anhydrase 4Homo sapiens (human)
cell surfaceCarbonic anhydrase 4Homo sapiens (human)
membraneCarbonic anhydrase 4Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 4Homo sapiens (human)
transport vesicle membraneCarbonic anhydrase 4Homo sapiens (human)
secretory granule membraneCarbonic anhydrase 4Homo sapiens (human)
brush border membraneCarbonic anhydrase 4Homo sapiens (human)
perinuclear region of cytoplasmCarbonic anhydrase 4Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 4Homo sapiens (human)
plasma membraneCarbonic anhydrase 4Homo sapiens (human)
extracellular regionCarbonic anhydrase 6Homo sapiens (human)
extracellular spaceCarbonic anhydrase 6Homo sapiens (human)
cytosolCarbonic anhydrase 6Homo sapiens (human)
extracellular exosomeCarbonic anhydrase 6Homo sapiens (human)
extracellular spaceCarbonic anhydrase 6Homo sapiens (human)
mitochondrial matrixCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
cytoplasmCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5A, mitochondrialHomo sapiens (human)
cytosolCarbonic anhydrase 7Homo sapiens (human)
cytoplasmCarbonic anhydrase 7Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 2J2Homo sapiens (human)
extracellular exosomeCytochrome P450 2J2Homo sapiens (human)
cytoplasmCytochrome P450 2J2Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2J2Homo sapiens (human)
virion membraneSpike glycoproteinSevere acute respiratory syndrome-related coronavirus
plasma membraneGuanine nucleotide-binding protein GHomo sapiens (human)
nucleolusCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 9Homo sapiens (human)
membraneCarbonic anhydrase 9Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 9Homo sapiens (human)
microvillus membraneCarbonic anhydrase 9Homo sapiens (human)
plasma membraneCarbonic anhydrase 9Homo sapiens (human)
fibrillar centerInositol hexakisphosphate kinase 1Homo sapiens (human)
nucleoplasmInositol hexakisphosphate kinase 1Homo sapiens (human)
cytosolInositol hexakisphosphate kinase 1Homo sapiens (human)
nucleusInositol hexakisphosphate kinase 1Homo sapiens (human)
cytoplasmInositol hexakisphosphate kinase 1Homo sapiens (human)
plasma membraneCanalicular multispecific organic anion transporter 1Homo sapiens (human)
cell surfaceCanalicular multispecific organic anion transporter 1Homo sapiens (human)
apical plasma membraneCanalicular multispecific organic anion transporter 1Homo sapiens (human)
intercellular canaliculusCanalicular multispecific organic anion transporter 1Homo sapiens (human)
apical plasma membraneCanalicular multispecific organic anion transporter 1Homo sapiens (human)
plasma membraneCarbonic anhydrase 14Homo sapiens (human)
membraneCarbonic anhydrase 14Homo sapiens (human)
basolateral plasma membraneCarbonic anhydrase 14Homo sapiens (human)
apical plasma membraneCarbonic anhydrase 14Homo sapiens (human)
plasma membraneCarbonic anhydrase 14Homo sapiens (human)
mitochondrionCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
mitochondrial matrixCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
mitochondrionCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
cytoplasmCarbonic anhydrase 5B, mitochondrialHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (709)

Assay IDTitleYearJournalArticle
AID1347126qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh30 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1347106qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for control Hh wild type fibroblast cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347103qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347118qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347091qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347128qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for OHS-50 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347100qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347090qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347116qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SJ-GBM2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347111qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347098qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347115qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB-EBc1 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1508630Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay2021Cell reports, 04-27, Volume: 35, Issue:4
A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID1347104qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347095qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347154Primary screen GU AMC qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347096qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for U-2 OS cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347117qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-37 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347114qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for DAOY cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347110qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for A673 cells)2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347124qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for RD cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347094qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347102qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347125qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh18 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347112qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-12 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347119qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for MG 63 (6-TG R) cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347089qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347121qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for control Hh wild type fibroblast cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347101qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347097qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347122qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for U-2 OS cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347092qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347113qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for LAN-5 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347107qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh30 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347108qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347129qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-SH cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347105qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347123qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347127qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347109qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB1643 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347099qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347093qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347411qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Mechanism Interrogation Plate v5.0 (MIPE) Libary2020ACS chemical biology, 07-17, Volume: 15, Issue:7
High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
AID588460High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, Validation Compound Set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588460High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, Validation Compound Set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588460High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, Validation Compound Set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588459High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, Validation compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588459High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, Validation compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588459High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, Validation compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID588461High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, Validation compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588461High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, Validation compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588461High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, Validation compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID681388TP_TRANSPORTER: inhibition of PAH uptake in Xenopus laevis oocytes2000The Journal of pharmacology and experimental therapeutics, Oct, Volume: 295, Issue:1
Interaction and transport of thiazide diuretics, loop diuretics, and acetazolamide via rat renal organic anion transporter rOAT1.
AID168613Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed as urinary output. at a dose of 14 mg/kg; 7.17/9.081986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID496817Antimicrobial activity against Trypanosoma cruzi2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID180082Antihypertensive activity determined as heart rate in SH rats, was reported at a dose of 100 mg/Kg1984Journal of medicinal chemistry, Dec, Volume: 27, Issue:12
N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as antihypertensive and diuretic agents.
AID21804Mean urinary output in rats when compound administered at 10 mg/kg po and vehicle dosed at 33.59 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID496826Antimicrobial activity against Entamoeba histolytica2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID1195371Inhibition of Anopheles gambiae carbonic anhydrase pre-incubated for 15 mins by stopped-flow CO2 hydration assay2015Bioorganic & medicinal chemistry, May-15, Volume: 23, Issue:10
The β-carbonic anhydrase from the malaria mosquito Anopheles gambiae is highly inhibited by sulfonamides.
AID40705The compound was tested for beta-2 adrenergic receptor blocking activity in dogs; NT is Not Tested1986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID58594The saluretic(Cl-) effect of compound was measured in dogs after iv administration at 3 mg/kg dose; Cl-mequiv/min=3031981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID17319Mean sodium excretion in rats when compound administered at 80 mg/kg po and vehicle dosed at 268.71 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID21605Compound was evaluated for diuretic activity, in female mongrel dogs by measuring volume of urine, after iv administration of 5 mg/kg (control/compound treatment results) Control = 21984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID743514Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides.
AID455986Permeability across human Caco-2 cells2009Bioorganic & medicinal chemistry, Oct-01, Volume: 17, Issue:19
Computational modeling of novel inhibitors targeting the Akt pleckstrin homology domain.
AID15976Antidiuretic activity was determined expressed as volume of urine excreted in mL was reported at a dose of 100 mg/Kg1984Journal of medicinal chemistry, Dec, Volume: 27, Issue:12
N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as antihypertensive and diuretic agents.
AID180388Diuretic activity by measuring the urinary output after 2 hr at the dose of 12 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1132617Natriuretic activity in rat assessed as per cage at 9 mg/kg, po1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID168822Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed in Na+, mequiv/6 hr at a dose of 55 mg/kg; 0.261/0.7351986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID196138Natriuretic activity in rats at 27 mg/kg of dosage; mequiv of Na1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID1061066Inhibition of Thalassiosira weissflogii delta carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sulfonamide inhibition studies of the δ-carbonic anhydrase from the diatom Thalassiosira weissflogii.
AID1194028Inhibition of recombinant Nostoc commune gamma-carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry, Apr-15, Volume: 23, Issue:8
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune.
AID188265Sodium salt excretion in conscious rat at the dose of 10 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1262266Inhibition of weddell seal alphaCA incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID19864Mean excretion of chloride in conscious rats at a dose of 30 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1091956Apparent hydrophobicity, log D of the compound in Octanol-buffer2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID21790Mean urinary output in rats (Control/Drug treatment value); value 24.1/39.51992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID16845Mean potassium excretion in rats when compound administered at 20 mg/kg po and vehicle dosed at 67.18 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID16935Mean urine volume excretion in conscious rats at a dose of 10 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1474167Liver toxicity in human assessed as induction of drug-induced liver injury by measuring verified drug-induced liver injury concern status2016Drug discovery today, Apr, Volume: 21, Issue:4
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
AID496818Antimicrobial activity against Trypanosoma brucei brucei2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID1142833Inhibition of human carbonic anhydrase-1 by stopped-flow CO2 hydration assay2014Bioorganic & medicinal chemistry, Jun-01, Volume: 22, Issue:11
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila.
AID180566Total Cl- milliequivalents excretion in diuretic test at the dose of 27 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID180395Diuretic activity by measuring the urinary output after 5 hr at the dose of 12 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1628038Inhibition of recombinant Plasmodium falciparum eta-carbonic anhydrase (181 to 538 residues) expressed in Escherichia coli artic express (DE3) preincubated for 15 mins by stop flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, 09-01, Volume: 26, Issue:17
Cloning, expression, purification and sulfonamide inhibition profile of the complete domain of the η-carbonic anhydrase from Plasmodium falciparum.
AID28924Effective permeability (Pe) across a hexadecane membrane (pH 6.8)2001Journal of medicinal chemistry, Mar-15, Volume: 44, Issue:6
High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes.
AID57191Compound was evaluated for diuretic activity, in female mongrel dogs by measuring amount of K+ in urine after iv administration of 5 mg/kg (control/compound treatment results) Control = 131984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1287517Inhibition of human carbonic anhydrase 1 incubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Apr-01, Volume: 26, Issue:7
Sulfonamide inhibition studies of the β-carbonic anhydrase from the newly discovered bacterium Enterobacter sp. B13.
AID190853Diuretic activity given as urinary output of 15 mg/kg perorally administered compound in rats1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID24184Distribution coefficient in octanol/water at pH 6.51998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID1079946Presence of at least one case with successful reintroduction. [column 'REINT' in source]
AID588214FDA HLAED, liver enzyme composite activity2004Current drug discovery technologies, Dec, Volume: 1, Issue:4
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
AID644379Inhibition of GST-tagged astrosclera willeyana Astrosclerin-3 expressed in Escherichia coli after 15 mins preincubation by stopped flow CO2 hydration assay2012Bioorganic & medicinal chemistry, Feb-15, Volume: 20, Issue:4
Cloning, characterization and sulfonamide inhibition studies of an α-carbonic anhydrase from the living fossil sponge Astrosclera willeyana.
AID16798Total electrolytic excretion of chlorine in urine of dogs after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID29359Ionization constant (pKa)2000Journal of medicinal chemistry, Jun-29, Volume: 43, Issue:13
QSAR model for drug human oral bioavailability.
AID180398Diuretic activity by measuring the urinary output after 5 hr at the dose of 3 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID743515Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides.
AID180598Compound was tested for the oral natriuretic activity in female rats at the dose 27 mg/kg; mequiv of Na+ x 100 / cage1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID1079934Highest frequency of acute liver toxicity observed during clinical trials, expressed as a percentage. [column '% AIGUE' in source]
AID1628036Inhibition of full length human cytosolic carbonic anhydrase 1 preincubated for 15 mins by stop flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, 09-01, Volume: 26, Issue:17
Cloning, expression, purification and sulfonamide inhibition profile of the complete domain of the η-carbonic anhydrase from Plasmodium falciparum.
AID17166Total electrolytic excretion of potassium in urine of dogs after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1079943Malignant tumor, proven histopathologically. Value is number of references indexed. [column 'T.MAL' in source]
AID19861Mean excretion of chloride in conscious rats at a dose of 1.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1132624Diuretic activity in dog assessed as chloride level in urine per min at 5 mg/kg, iv relative to control1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID588216FDA HLAED, serum glutamic oxaloacetic transaminase (SGOT) increase2004Current drug discovery technologies, Dec, Volume: 1, Issue:4
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
AID230526Ratio of saluretic activity for Na+ over saluretic activity of K+ in rats after peroral administration of 30 mg/kg of compound1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID188264Sodium salt excretion in conscious rat at the dose of 1.0 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID51758Compound was evaluated for diuretic activity in chimpanzee measured as clearance of insulin and urate after peroral administration of 5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID19869Mean excretion of potassium in conscious rats at a dose of 10 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID17544Total electrolytic excretion of sodium in urine of dogs after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID180578Total K+ milliequivalents excretion in diuretic test at the dose of 3 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID21775volume of urine at 9 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID176006The saluretic(Cl-) effect of compound was measured in rats after oral administration at 3 mg/kg dose; Cl-mequiv*100/cage=141981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID19875Mean excretion of sodium in conscious rats at a dose of 10 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1268962Inhibition of recombinant human carbonic anhydrase-1 by stopped flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, Jan-15, Volume: 26, Issue:2
Sulfonamide inhibition studies of the α-carbonic anhydrase from the gammaproteobacterium Thiomicrospira crunogena XCL-2, TcruCA.
AID169988Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of K+x 100 / cage at 9 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID15928Mean Chlorine excretion in rats when compound administered at 0 mg/kg po and vehicle dosed at 0 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID726232Inhibition of Trypanosoma cruzi CL Brener recombinant alpha-carbonic anhydrase expressed in insect Sf9 cell Baculovirus system by stopped flow CO2 hydration assay2013Journal of medicinal chemistry, Feb-28, Volume: 56, Issue:4
Cloning, characterization, and sulfonamide and thiol inhibition studies of an α-carbonic anhydrase from Trypanosoma cruzi, the causative agent of Chagas disease.
AID1660451Diuretic activity in normotensive Wistar rat assessed as increase in urine volume at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID180572Total Cl-mequiv excretion in diuretic test at the dose of 3 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID14155Oral diuretic activity was evaluated by measuring Na+ excretion in dog at 5 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID174415Change in blood pressure (Initial blood pressure- Post drug blood pressure)1987Journal of medicinal chemistry, Dec, Volume: 30, Issue:12
[(6,7-Dichlorobenzo[b]thien-5-yl)oxy]acetic acids and 1,1-dioxides. 1. A structurally novel class of diuretics with hypotensive activity.
AID168200Saluretic activity was evaluated for Na+ by flame photometry at 30 mg/kg perorally1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID230528Ratio of saluretic activity for Na+ over saluretic activity of K+ in rats after peroral administration of 8 mg/kg of compound1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID168618Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed as urinary output. at a dose of 27 mg/kg; 7.17/9.751986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID156204Binding to POPC/GMI liposomes using biosensor system2000Journal of medicinal chemistry, Jun-01, Volume: 43, Issue:11
SPR biosensor studies of the direct interaction between 27 drugs and a liposome surface: correlation with fraction absorbed in humans.
AID1660387Diuretic activity in normotensive Wistar rat assessed as urinary chloride excretion at 10 mg/kg, po administered via gavage after 8 hrs (Rvb = 135.10 to 143.70 mmol/L)2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID588219FDA HLAED, gamma-glutamyl transferase (GGT) increase2004Current drug discovery technologies, Dec, Volume: 1, Issue:4
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
AID1195370Inhibition of human carbonic anhydrase 2 pre-incubated for 15 mins by stopped-flow CO2 hydration assay2015Bioorganic & medicinal chemistry, May-15, Volume: 23, Issue:10
The β-carbonic anhydrase from the malaria mosquito Anopheles gambiae is highly inhibited by sulfonamides.
AID186961Potassium salt excretion in conscious rat at the dose of 30 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID497005Antimicrobial activity against Pneumocystis carinii2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID16596Oral diuretic activity was evaluated by measuring Cl- excretion in dog at 1 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID21809Mean urinary output in rats when compound administered at 160 mg/kg po and vehicle dosed at 594.07 umol/kg; Not determined1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID21824Mean urinary output in rats when compound administered at 5 mg/kg po and vehicle dosed at 16.79 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID16696Mean potassium excretion in rats when compound administered at 160 mg/kg po and vehicle dosed at 594.07 umol/kg; Not determined1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID13770Oral diuretic activity was evaluated by measuring K+ excretion in Rat at 27 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID174281Compound was tested for antihypertensive activity in rat after 1 hr postdose1986Journal of medicinal chemistry, Jun, Volume: 29, Issue:6
Synthesis, saludiuretic, and antihypertensive activity of 6,7-disubstituted 1(2H)- and 3,4-dihydro-1(2H)-phthalazinones.
AID180562Total Cl- milliequivalents excretion in diuretic test at the dose of 12 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID16005Compound administered orally at a dose of 5 mg/kg was evaluated for salidiuretic activity measured as sodium ion excretion in Rat1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID230248Ratio of Na+ to K+ excretion at dose1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1079940Granulomatous liver disease, proven histopathologically. Value is number of references indexed. [column 'GRAN' in source]
AID1660491In vivo antioxidant activity in Wistar rat model of hypertension-induced oxidative stress assessed as reduction in reactive oxygen species generation in renal tissue at 10 mg/kg, po administered via gavage for 7 days by DCFH-DA probe based fluorimetric as2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID1190065Inhibition of Plasmodium falciparum Eta-carbonic anhydrase pre-incubated for 15 mins before CO2 substrate addition by stopped-flow CO2 hydration assay2015Bioorganic & medicinal chemistry, Feb-01, Volume: 23, Issue:3
Sulfonamide inhibition studies of the η-class carbonic anhydrase from the malaria pathogen Plasmodium falciparum.
AID21584Urinary sodium 6 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID16565Oral diuretic activity was evaluated by measuring Cl- excretion in Rat at 27 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID679525TP_TRANSPORTER: inhibition of PAH uptake (PAH: 1 uM, Hydrochlorothiazide: 100 uM) in Xenopus laevis oocytes1999Biochemical and biophysical research communications, Feb-16, Volume: 255, Issue:2
Molecular cloning and characterization of two novel human renal organic anion transporters (hOAT1 and hOAT3).
AID174953Time taken for the decrease in arterial pressure was measured1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID16081Mean Chlorine excretion in rats when compound administered at 80 mg/kg po and vehicle dosed at 268.71 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID48105Binding activity against human Carbonic anhydrase II (hCAII)2002Journal of medicinal chemistry, Aug-15, Volume: 45, Issue:17
Successful virtual screening for novel inhibitors of human carbonic anhydrase: strategy and experimental confirmation.
AID1268963Inhibition of recombinant human carbonic anhydrase-2 by stopped flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, Jan-15, Volume: 26, Issue:2
Sulfonamide inhibition studies of the α-carbonic anhydrase from the gammaproteobacterium Thiomicrospira crunogena XCL-2, TcruCA.
AID16936Mean urine volume excretion in conscious rats at a dose of 100 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID176013The saluretic(K+) effect of compound was measured in rats after oral administration at 3 mg/kg dose; K+mequiv*100/cage=141981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID481446Effective permeability across human jejunum2010Journal of medicinal chemistry, May-13, Volume: 53, Issue:9
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
AID13797Oral diuretic activity was evaluated by measuring K+ excretion in dog at 10 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1079949Proposed mechanism(s) of liver damage. [column 'MEC' in source]
AID588218FDA HLAED, lactate dehydrogenase (LDH) increase2004Current drug discovery technologies, Dec, Volume: 1, Issue:4
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
AID1473740Inhibition of human MRP3 overexpressed in Sf9 insect cell membrane vesicles assessed as uptake of [3H]-estradiol-17beta-D-glucuronide in presence of ATP and GSH measured after 10 mins by membrane vesicle transport assay2013Toxicological sciences : an official journal of the Society of Toxicology, Nov, Volume: 136, Issue:1
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
AID22028Tested for the diuretic activity by measuring the urinary volume after peroral administering 10.1 uM/Kg of drug in dogs1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1453410Inhibition of Francisella tularensis beta-carbonic anhydrase assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 secs by stopped-flow assay
AID567091Drug absorption in human assessed as human intestinal absorption rate2011European journal of medicinal chemistry, Jan, Volume: 46, Issue:1
Prediction of drug intestinal absorption by new linear and non-linear QSPR.
AID169991Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Na+x 100 / cage at 81 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1079945Animal toxicity known. [column 'TOXIC' in source]
AID21578Urinary sodium 3h after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID218755Compound was tested for diuretic activity in dogs at 5 mg/kg dose after intravenous administration measured as microequivalent of K+/minute; 15/33 (Control/Drug treated)1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID17580Total electrolytic excretion of sodium in urine of rats after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID588215FDA HLAED, alkaline phosphatase increase2004Current drug discovery technologies, Dec, Volume: 1, Issue:4
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
AID1132627Diuretic activity in dog assessed as chloride level in urine volume at 5 mg/kg, iv relative to control1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID1142836Inhibition of Legionella pneumophilia subsp. Pneumophila strain Philadelphia-1 carbonic anhydrase-1 assessed as CO2 hydrase activity by stopped-flow assay2014Bioorganic & medicinal chemistry, Jun-01, Volume: 22, Issue:11
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila.
AID21602Volume of urine 6 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID58598The saluretic(Na+) effect of compound was measured in dogs after iv administration at 3 mg/kg dose; Na+ mequiv/min=2791981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID496831Antimicrobial activity against Cryptosporidium parvum2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID15987Salidiuretic activity in dog following i.v. dosing at 5 mg/kg1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID237416Distribution coeeficient for the compound at pH7.4 (Log D7.4) 2004Journal of medicinal chemistry, Jul-29, Volume: 47, Issue:16
Contribution of ionization and lipophilicity to drug binding to albumin: a preliminary step toward biodistribution prediction.
AID187998Hypotensive activity after 50 mg/kg oral dose in rats (Change in blood pressure after treatment (day/hours))1987Journal of medicinal chemistry, Dec, Volume: 30, Issue:12
[(6,7-Dichlorobenzo[b]thien-5-yl)oxy]acetic acids and 1,1-dioxides. 1. A structurally novel class of diuretics with hypotensive activity.
AID16699Mean potassium excretion in rats when compound administered at 2.5 mg/kg po and vehicle dosed at 8.4 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID230476Ratio of Total electrolytic excretion of sodium and potassium in urine of rats after peroral administration of 34.0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID169985Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of K+x 100 / cage at 27 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID186829Potassium salt excretion in conscious rat at the dose of 0.3 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID625283Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for elevated liver function tests2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID588217FDA HLAED, serum glutamic pyruvic transaminase (SGPT) increase2004Current drug discovery technologies, Dec, Volume: 1, Issue:4
Assessment of the health effects of chemicals in humans: II. Construction of an adverse effects database for QSAR modeling.
AID188268Sodium salt excretion in conscious rat at the dose of 30 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID26400pKa value of the compound. (extrapolated value)1998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID1244132Induction of diuresis in Sprague-Dawley rat at 25 mg/kg, po after 4 hrs relative to control2015ACS medicinal chemistry letters, Jul-09, Volume: 6, Issue:7
Discovery of a Potent and Selective ROMK Inhibitor with Pharmacokinetic Properties Suitable for Preclinical Evaluation.
AID20826Na+ excretion mequiv/kg in saline-loaded mice administered at a dose 30 ml/kg perorally1984Journal of medicinal chemistry, Aug, Volume: 27, Issue:8
Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: high-ceiling diuretics with uricosuric activity.
AID28234% absorbed in human GI-tract2001Journal of medicinal chemistry, Mar-15, Volume: 44, Issue:6
High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes.
AID1194027Inhibition of recombinant Porphyromonas gingivalis gamma-carbonic anhydrase by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry, Apr-15, Volume: 23, Issue:8
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune.
AID467612Fraction unbound in human plasma2009European journal of medicinal chemistry, Nov, Volume: 44, Issue:11
Prediction of volume of distribution values in human using immobilized artificial membrane partitioning coefficients, the fraction of compound ionized and plasma protein binding data.
AID1647951prevention of heart failure in verapamil treated zebrafish AB assessed as efficacy on venous congestion at 0.5 ug/ml preincubated for 4.5 hrs followed by verapamil treatment and measured after 30 mins relative to verapamil alone
AID232096Compound was tested for natriuretic activity in chimpanzee at 5 mg/kg dose activity is measured as ratio of clearance of urate / insulin; Curate/Cinulin1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID16975Total electrolytic excretion of chlorine in urine of rats after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID743513Inhibition of Helicobacter pylori recombinant alpha carbonic anhydrase preincubated for 15 mins by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides.
AID13983Oral diuretic activity was evaluated by measuring Na+ excretion in dog at 10 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID288184Permeability coefficient through artificial membrane in presence of unstirred water layer by PAMPA2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID196142Natriuretic activity in rats at 9 mg/kg of dosage; mequiv of Na1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID13764Oral diuretic activity was evaluated by measuring Cl- excretion in dog at 5 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID180391Diuretic activity by measuring the urinary output after 2 hr at the dose of 27 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID180564Total Cl- milliequivalents excretion in diuretic test at the dose of 1 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID13788Oral diuretic activity was evaluated by measuring K+ excretion in Rat at 9 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID173380The saluretic(K+) effect of compound was measured in rats after oral administration at 81 mg/kg dose; K+mequiv*100/cage=141981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID1204106Inhibition of recombinant Streptococcus mutans UA159 beta-carbonic anhydrase expressed in Escherichia coli Arctic cells preincubated for 15 mins by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Jun-01, Volume: 25, Issue:11
Sulfonamide inhibition study of the β-class carbonic anhydrase from the caries producing pathogen Streptococcus mutans.
AID21773volume of urine at 3 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1132623Diuretic activity in dog assessed as sodium level in urine per min at 5 mg/kg, iv relative to control1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID21772volume of urine at 27 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID28925Highest effective permeability across hexadecane membrane (pH 4-8)2001Journal of medicinal chemistry, Mar-15, Volume: 44, Issue:6
High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes.
AID180604Compound was tested for the oral natriuretic activity in female rats at the dose 9 mg/kg; mequiv of Na+ x 100 / cage1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID17300Mean sodium excretion in rats when compound administered at 160 mg/kg po and vehicle dosed at 594.07 umol/kg; Not determined1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID496823Antimicrobial activity against Trichomonas vaginalis2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID180583Total Na+ milliequivalents excretion in diuretic test at the dose of 12 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID230277Ratio of Total electrolytic excretion of sodium and potassium in urine of dogs after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID51764Compound was tested for natriuretic activity in chimpanzee at 5 mg/kg dose activity is measured as microequivalent of Na+/minute; muequiv of Na+/min1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID173384The saluretic(Na+) effect of compound was measured in rats after oral administration at 81 mg/kg dose; Na+ mequiv*100/cage1981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID1392219Effective permeability of the compound by PAMPA assay2018Journal of medicinal chemistry, 05-24, Volume: 61, Issue:10
N
AID18861GOF value represents multisets of log P data1998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID21264Effective permeability measured in human.1998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID644380Inhibition of human recombinant carbonic anhydrase 1 after 15 mins by stopped flow CO2 hydration assay2012Bioorganic & medicinal chemistry, Feb-15, Volume: 20, Issue:4
Cloning, characterization and sulfonamide inhibition studies of an α-carbonic anhydrase from the living fossil sponge Astrosclera willeyana.
AID481440Dissociation constant, pKa of the compound2010Journal of medicinal chemistry, May-13, Volume: 53, Issue:9
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
AID1188138Inhibition of Porphyromonas gingivalis Gamma-carbonic anhydrase compound preincubated for 15 mins by stopped flow CO2 hydrase assay method2014Bioorganic & medicinal chemistry, Sep-01, Volume: 22, Issue:17
Sulfonamide inhibition study of the carbonic anhydrases from the bacterial pathogen Porphyromonas gingivalis: the β-class (PgiCAb) versus the γ-class (PgiCA) enzymes.
AID19874Mean excretion of sodium in conscious rats at a dose of 1.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID19870Mean excretion of potassium in conscious rats at a dose of 100 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID169983Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Cl-x 100 / cage at 81 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID16983Total electrolytic excretion of chlorine in urine of rats after peroral administration of 34.0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID51738Compound was evaluated for diuretic activity in chimpanzee measured as increase in the number of microequivalents of Na+ /min at 5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1434428Inhibition of human carbonic anhydrase 2 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 sec by Line-Weaver Burk plot analysis
AID1474166Liver toxicity in human assessed as induction of drug-induced liver injury by measuring severity class index2016Drug discovery today, Apr, Volume: 21, Issue:4
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
AID186832Potassium salt excretion in conscious rat at the dose of 100 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID459002Binding affinity to subsite C/C' in S1S2 domain of GluA2 receptor expressed in Escherichia coli by crystallography2010Journal of medicinal chemistry, Mar-11, Volume: 53, Issue:5
Piracetam defines a new binding site for allosteric modulators of alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptors.
AID180573Total K+ milliequivalents excretion in diuretic test at the dose of 12 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID51604Compound was evaluated for diuretic activity in chimpanzee measured as increase in the number of microequivalents of K+ /min at 1.5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1660499Renal protective activity in spontaneous hypertensive Wistar rat assessed as reduction in hypertension-induced mesangial space disarrangement at 10 mg/kg, po administered via gavage for 7 days by hematoxylin and eosin staining based microscopic analysis2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID21590Volume of urine 1 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1188134Inhibition of human recombinant Carbonic anhydrase 1 compound preincubated for 15 mins by stopped flow CO2 hydrase assay method2014Bioorganic & medicinal chemistry, Sep-01, Volume: 22, Issue:17
Sulfonamide inhibition study of the carbonic anhydrases from the bacterial pathogen Porphyromonas gingivalis: the β-class (PgiCAb) versus the γ-class (PgiCA) enzymes.
AID16592Oral diuretic activity was evaluated by measuring Cl- excretion in dog at 10 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID19868Mean excretion of potassium in conscious rats at a dose of 1.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1149927Natriuretic activity in chimpanzee assessed as change sodium level in urine measured per min at 5 mg/kg, po1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID186857Maximum fall in mean arterial blood pressure was measured in SH rats when compound was administered at 20 mg/kg perorally1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1660452Diuretic activity in spontaneous hypertensive Wistar rat assessed as increase in urine volume at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID13782Oral diuretic activity was evaluated by measuring K+ excretion in Rat at 81 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID193070Duration of effect was measured in hypertensive rat1981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID1453413Inhibition of human carbonic anhydrase-2 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 secs by stopped-flow assay
AID169990Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Na+x 100 / cage at 3 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID588213Literature-mined compound from Fourches et al multi-species drug-induced liver injury (DILI) dataset, effect in non-rodents2010Chemical research in toxicology, Jan, Volume: 23, Issue:1
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
AID19863Mean excretion of chloride in conscious rats at a dose of 100 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID168630Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed as urinary output. at a dose of 55 mg/kg; 7.17/9.581986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID28681Partition coefficient (logD6.5)2000Journal of medicinal chemistry, Jun-29, Volume: 43, Issue:13
QSAR model for drug human oral bioavailability.
AID21599Volume of urine 4 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID612726Inhibition of human recombinant carbonic anhydrase 2 at pH 7.5 by stopped flow CO2 hydration assay2011Bioorganic & medicinal chemistry, Aug-15, Volume: 19, Issue:16
Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates.
AID190428Evaluated for the saluretic property in rats after oral administration; score represents micro equivalents of Na+ excreted at a given mg/kg dose1981Journal of medicinal chemistry, Sep, Volume: 24, Issue:9
2-(Aminomethyl)phenols, a new class of saluretic agents. 3. Effects of functional group reorientation and modification.
AID1647949Prevention of heart failure in verapamil treated zebrafish AB assessed as efficacy on heart dilation at 0.5 ug/ml preincubated for 4.5 hrs followed by verapamil treatment and measured after 30 mins relative to verapamil alone
AID29813Oral bioavailability in human2000Journal of medicinal chemistry, Jun-29, Volume: 43, Issue:13
QSAR model for drug human oral bioavailability.
AID39749In vitro inhibitory activity against angiotensin I converting enzyme (ACE) in dog1990Journal of medicinal chemistry, Jun, Volume: 33, Issue:6
Angiotensin-converting enzyme inhibitors. 9. Novel [[N-(1-carboxy-3-phenylpropyl)amino]acyl]glycine derivatives with diuretic activity.
AID19866Mean urine volume excretion in conscious rats at a dose of 0.3 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID612725Inhibition of human recombinant carbonic anhydrase 1 at pH 7.5 by stopped flow CO2 hydration assay2011Bioorganic & medicinal chemistry, Aug-15, Volume: 19, Issue:16
Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates.
AID1079944Benign tumor, proven histopathologically. Value is number of references indexed. [column 'T.BEN' in source]
AID496832Antimicrobial activity against Trypanosoma brucei rhodesiense2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID13987Oral diuretic activity was evaluated by measuring Na+ excretion in dog at 1 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID711212Inhibition of recombinant Vibrio cholerae carbonic anhydrase expressed in Escherichia coli (DE3) preincubated for 15 mins by stopped-flow CO2 hydrase assay2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
DNA cloning, characterization, and inhibition studies of an α-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID188263Sodium salt excretion in conscious rat at the dose of 0.3 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1061067Inhibition of Porphyromonas gingivalis recombinant gamma-carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sulfonamide inhibition studies of the δ-carbonic anhydrase from the diatom Thalassiosira weissflogii.
AID13776Oral diuretic activity was evaluated by measuring K+ excretion in Rat at 3 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1294128Increase in diuresis in Sprague-Dawley rat at 10 mg/kg, po measured after 4 hrs relative to control2016Bioorganic & medicinal chemistry letters, May-01, Volume: 26, Issue:9
Differentiation of ROMK potency from hERG potency in the phenacetyl piperazine series through heterocycle incorporation.
AID17307Mean sodium excretion in rats when compound administered at 20 mg/kg po and vehicle dosed at 67.18 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID230469Ratio of Total electrolytic excretion of sodium and potassium in urine of rats after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID13965Oral diuretic activity was evaluated by measuring Na+ excretion in Rat at 3 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID190622Post dosing time interval of maximum activity1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID190867Compound was tested for urinary volume excretion in conscious rat at the dose of 3.0 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1079931Moderate liver toxicity, defined via clinical-chemistry results: ALT or AST serum activity 6 times the normal upper limit (N) or alkaline phosphatase serum activity of 1.7 N. Value is number of references indexed. [column 'BIOL' in source]
AID239780Percentage plasma protein binding towards human serum albumin2005Journal of medicinal chemistry, Apr-07, Volume: 48, Issue:7
Predicting human serum albumin affinity of interleukin-8 (CXCL8) inhibitors by 3D-QSPR approach.
AID409956Inhibition of mouse brain MAOB2008Journal of medicinal chemistry, Nov-13, Volume: 51, Issue:21
Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.
AID588209Literature-mined public compounds from Greene et al multi-species hepatotoxicity modelling dataset2010Chemical research in toxicology, Jul-19, Volume: 23, Issue:7
Developing structure-activity relationships for the prediction of hepatotoxicity.
AID13801Oral diuretic activity was evaluated by measuring K+ excretion in dog at 1 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID612731Inhibition of Salmonella Typhimurium recombinant carbonic anhydrase 1 at pH 8.3 by stopped flow CO2 hydration assay2011Bioorganic & medicinal chemistry, Aug-15, Volume: 19, Issue:16
Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates.
AID21575Urinary sodium 2 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID63431Volume of urine in dog1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID588211Literature-mined compound from Fourches et al multi-species drug-induced liver injury (DILI) dataset, effect in humans2010Chemical research in toxicology, Jan, Volume: 23, Issue:1
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
AID51759Compound was evaluated for diuretic activity in chimpanzee measured as increase in the number of microequivalents of Cl- electrolyte/min at 5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID17303Mean sodium excretion in rats when compound administered at 2.5 mg/kg po and vehicle dosed at 8.4 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID21596Volume of urine 3h after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1244133Induction of natriuresis in Sprague-Dawley rat at 25 mg/kg, po after 4 hrs relative to control2015ACS medicinal chemistry letters, Jul-09, Volume: 6, Issue:7
Discovery of a Potent and Selective ROMK Inhibitor with Pharmacokinetic Properties Suitable for Preclinical Evaluation.
AID169989Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Na+x 100 / cage at 27 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID17337Na+ excretion mequiv/kg in saline-loaded mice administered at a dose 3 ml/kg perorally1984Journal of medicinal chemistry, Aug, Volume: 27, Issue:8
Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: high-ceiling diuretics with uricosuric activity.
AID346025Binding affinity to beta cyclodextrin2009Bioorganic & medicinal chemistry, Jan-15, Volume: 17, Issue:2
Convenient QSAR model for predicting the complexation of structurally diverse compounds with beta-cyclodextrins.
AID16577Oral diuretic activity was evaluated by measuring Cl- excretion in Rat at 81 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID230525Ratio of saluretic activity for Na+ over saluretic activity of K+ in rats after peroral administration of 15 mg/kg of compound1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID21802Mean urinary output in rats when compound administered at 0 mg/kg po and vehicle dosed at 0 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID180400Diuretic activity by measuring the urinary output after 5 hr at the dose of 9 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID243230Binding affinity towards human serum albumin2005Journal of medicinal chemistry, Apr-07, Volume: 48, Issue:7
Predicting human serum albumin affinity of interleukin-8 (CXCL8) inhibitors by 3D-QSPR approach.
AID186357Antihypertensive activity in SH rats, and mean arterial blood pressure was reported at a dose of 100 mg/Kg1984Journal of medicinal chemistry, Dec, Volume: 27, Issue:12
N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as antihypertensive and diuretic agents.
AID1474838Antihypertensive activity in rat spontaneous hypertensive model assessed as change in systolic blood pressure at 25 mg/kg, po qd measured after 3 days2017Bioorganic & medicinal chemistry letters, 06-01, Volume: 27, Issue:11
Improvement of hERG-ROMK index of spirocyclic ROMK inhibitors through scaffold optimization and incorporation of novel pharmacophores.
AID1660502Anti-urolithic activity in normotensive Wistar rats assessed as reduction in CaOx crystal formation in cumulative urine at 10 mg/kg, po administered via gavage in presence of sodium oxalate by Neubauer counting chamber method relative to control2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID1660498Renal protective activity in spontaneous hypertensive Wistar rat assessed as reduction in hypertension-induced Bowman's capsule thickening at 10 mg/kg, po administered via gavage for 7 days by hematoxylin and eosin staining based microscopic analysis2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID625291Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for liver function tests abnormal2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID21812Mean urinary output in rats when compound administered at 2.5 mg/kg po and vehicle dosed at 8.4 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID588212Literature-mined compound from Fourches et al multi-species drug-induced liver injury (DILI) dataset, effect in rodents2010Chemical research in toxicology, Jan, Volume: 23, Issue:1
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
AID186855Maximum fall in mean arterial blood pressure was measured in SH rats when compound was administered at 10 mg/kg perorally1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID230295Ratio of Total electrolytic excretion of sodium and potassium in urine of rats after peroral administration of 0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID168812Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed in Na+, mequiv/6 hr at a dose of 27 mg/kg; 0.261/0.7421986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID176008The saluretic(Cl-) effect of compound was measured in rats after oral administration at 81 mg/kg dose; Cl-mequiv*100/cage=141981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID16583Oral diuretic activity was evaluated by measuring Cl- excretion in Rat at 9 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID230250Ratio of Na+ to k+ excretion at above dose; Not determined1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID42033Compound was tested for beta-1 adrenergic receptor blocking activity in dogs; NT is Not Tested1986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID1149928Ratio of change in urate excretion to change in inulin excretion in chimpanzee in urine at 5 mg/kg, po1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID592681Apparent permeability across human Caco2 cell membrane after 2 hrs by LC-MS/MS analysis2011Bioorganic & medicinal chemistry, Apr-15, Volume: 19, Issue:8
QSAR-based permeability model for drug-like compounds.
AID28679Partition coefficient (logD6.8)2001Journal of medicinal chemistry, Mar-15, Volume: 44, Issue:6
High-throughput permeability pH profile and high-throughput alkane/water log P with artificial membranes.
AID17293Mean sodium excretion in rats when compound administered at 0 mg/kg po and vehicle dosed at 0 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1262263Inhibition of human CA1 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID1660366Diuretic activity in normotensive Wistar rat assessed as urine conductivity at 10 mg/kg, po administered via gavage after 8 hrs (Rvb = 19.54 +/- 0.98 mS/cm)2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID22029Tested for the diuretic activity by measuring the urinary volume after peroral administering 10.1 uM/Kg of drug in rats1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID51587Compound was tested for the oral diuretic activity in chimpanzee at the dose 5 mg/kg expressed as excretion rate in microequiv of Cl-/min1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID1268965Inhibition of recombinant Thiomicrospira crunogena XCL-2 carbonic anhydrase by stopped flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, Jan-15, Volume: 26, Issue:2
Sulfonamide inhibition studies of the α-carbonic anhydrase from the gammaproteobacterium Thiomicrospira crunogena XCL-2, TcruCA.
AID1275911Inhibition of Vibrio cholerae alpha-carbonic anhydrase using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry, Mar-01, Volume: 24, Issue:5
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID1808092Drug metabolism in human gut microbes assessed as metabolite formation by LC-MS/MS analysis2021Journal of medicinal chemistry, 12-09, Volume: 64, Issue:23
Searching for New Microbiome-Targeted Therapeutics through a Drug Repurposing Approach.
AID1275912Inhibition of human Carbonic anhydrase2 using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry, Mar-01, Volume: 24, Issue:5
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID16062Mean Chlorine excretion in rats when compound administered at 160 mg/kg po and vehicle dosed at 594.07 umol/kg; Not determined1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID288185Permeability coefficient through artificial membrane in presence of stirred water layer2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1240217Inhibition of human recombinant carbonic anhydrase-2 by stopped flow CO2 hydrase assay method2015Bioorganic & medicinal chemistry letters, Sep-01, Volume: 25, Issue:17
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Pseudoalteromonas haloplanktis.
AID496825Antimicrobial activity against Leishmania mexicana2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID13969Oral diuretic activity was evaluated by measuring Na+ excretion in Rat at 81 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1061170Inhibition of Porphyromonas gingivalis gamma-carbonic anhydrase expressed in Escherichia coli preincubated for 15 mins by stopped flow CO2 hydration assay2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the oral pathogen Porphyromonas gingivalis.
AID1188136Inhibition of Helicobacter pylori Beta-carbonic anhydrase compound preincubated for 15 mins by stopped flow CO2 hydrase assay method2014Bioorganic & medicinal chemistry, Sep-01, Volume: 22, Issue:17
Sulfonamide inhibition study of the carbonic anhydrases from the bacterial pathogen Porphyromonas gingivalis: the β-class (PgiCAb) versus the γ-class (PgiCA) enzymes.
AID288192Partition coefficient, log P of the compound2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1808091Drug metabolism in mini gut model assessed as metabolite formation by LC-MS/MS analysis2021Journal of medicinal chemistry, 12-09, Volume: 64, Issue:23
Searching for New Microbiome-Targeted Therapeutics through a Drug Repurposing Approach.
AID180397Diuretic activity by measuring the urinary output after 5 hr at the dose of 27 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID481442Transcellular permeability at pH 6.5 calculated from in vitro P app values in Caco-2 and/or MDCK cells2010Journal of medicinal chemistry, May-13, Volume: 53, Issue:9
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
AID176010The saluretic(K+) effect of compound was measured in rats after oral administration at 27 mg/kg dose; K+mequiv*100/cage=141981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID13979Oral diuretic activity was evaluated by measuring Na+ excretion in dog at 0.3 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1188135Inhibition of human recombinant Carbonic anhydrase 2 compound preincubated for 15 mins by stopped flow CO2 hydrase assay method2014Bioorganic & medicinal chemistry, Sep-01, Volume: 22, Issue:17
Sulfonamide inhibition study of the carbonic anhydrases from the bacterial pathogen Porphyromonas gingivalis: the β-class (PgiCAb) versus the γ-class (PgiCA) enzymes.
AID16691Mean potassium excretion in rats when compound administered at 10 mg/kg po and vehicle dosed at 33.59 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID404304Effect on human MRP2-mediated estradiol-17-beta-glucuronide transport in Sf9 cells inverted membrane vesicles relative to control2008Journal of medicinal chemistry, Jun-12, Volume: 51, Issue:11
Prediction and identification of drug interactions with the human ATP-binding cassette transporter multidrug-resistance associated protein 2 (MRP2; ABCC2).
AID58596The saluretic(K+) effect of compound was measured in dogs after iv administration at 3 mg/kg dose; K+mequiv/min=201981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID51598Compound was evaluated for diuretic activity in chimpanzee measured as increase in the number of microequivalents of Cl- electrolyte/min at 1.5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1132615Diuretic activity in dog assessed as potassium level in urine per min at 5 mg/kg, iv relative to control1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID180588Total Na+ milliequivalents excretion in diuretic test at the dose of 3 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID625289Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for liver disease2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID168459Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed as urinary output. at a dose of 110 mg/kg; 7.17/11.201986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID625285Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatic necrosis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID1660460Diuretic activity in normotensive Wistar rat assessed as increase in urinary sodium excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID57180Compound was evaluated for diuretic activity, administered orally in female mongrel dogs (5 mg/kg) measured as milliequivalents of K1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID168807Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed in Na+, mequiv/6 hr at a dose of 14 mg/kg; 0.261/0.6951986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID1194024Inhibition of human recombinant carbonic anhydrase 1 by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry, Apr-15, Volume: 23, Issue:8
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune.
AID1132619Natriuretic activity in rat assessed as per cage at 81 mg/kg, po1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID218757Compound was tested for diuretic activity in dogs at 5 mg/kg dose after intravenous administration, activity is expressed as urine volume; 1/31981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID1210069Inhibition of human recombinant CYP2J2 assessed as reduction in astemizole O-demethylation by LC-MS/MS method2013Drug metabolism and disposition: the biological fate of chemicals, Jan, Volume: 41, Issue:1
Discovery and characterization of novel, potent, and selective cytochrome P450 2J2 inhibitors.
AID175998The saluretic (Na+) effect of compound was measured in rats after oral administration at 27 mg/kg dose; Na+ mequiv*100/cage1981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID22026Tested for the diuretic activity by measuring the urinary volume after peroral administering 1.01 uM/Kg of drug in rats1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1079939Cirrhosis, proven histopathologically. Value is number of references indexed. [column 'CIRRH' in source]
AID22055Tested for the diuretic activity by measuring the urinary volume after peroral administering 3.40 uM/Kg of drug in dogs1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID778725Inhibition of recombinant Leishmania donovani chagasi beta-carbonic anhydrase expressed in baculovirus infected insect Sf9 cells incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2013Journal of medicinal chemistry, Sep-26, Volume: 56, Issue:18
Cloning, characterization, and inhibition studies of a β-carbonic anhydrase from Leishmania donovani chagasi, the protozoan parasite responsible for leishmaniasis.
AID22211Tested for the diuretic activity by measuring the urinary volume after peroral administering 34.0 uM/Kg of drug in rats1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1091957Apparent permeability of the compound by PAMPA2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID1660462Diuretic activity in normotensive Wistar rat assessed as decrease in urinary calcium excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID625288Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for jaundice2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID1287520Inhibition of recombinant Enterobacter sp. B13 beta carbonic anhydrase incubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Apr-01, Volume: 26, Issue:7
Sulfonamide inhibition studies of the β-carbonic anhydrase from the newly discovered bacterium Enterobacter sp. B13.
AID17745Total electrolytic excretion of sodium in urine of rats after peroral administration of 34.0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1275910Inhibition of Vibrio cholerae beta-carbonic anhydrase using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry, Mar-01, Volume: 24, Issue:5
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID16004Evaluated for salidiuretic activity measured as sodium ion excretion in Rat, administered orally at a dose of 50 mg/kg1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID230274Ratio of Total electrolytic excretion of sodium and potassium in urine of dogs after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID230446Ratio of Total electrolytic excretion of sodium and potassium in urine of rats after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1079933Acute liver toxicity defined via clinical observations and clear clinical-chemistry results: serum ALT or AST activity > 6 N or serum alkaline phosphatases activity > 1.7 N. This category includes cytolytic, choleostatic and mixed liver toxicity. Value is
AID196139Natriuretic activity in rats at 3 mg/kg of dosage; mequiv of Na1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID1294129Increase in naturesis in Sprague-Dawley rat at 10 mg/kg, po measured after 4 hrs relative to control2016Bioorganic & medicinal chemistry letters, May-01, Volume: 26, Issue:9
Differentiation of ROMK potency from hERG potency in the phenacetyl piperazine series through heterocycle incorporation.
AID1660467Diuretic activity in spontaneous hypertensive Wistar rat assessed as increase in urinary potassium excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID169986Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of K+x 100 / cage at 3 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID17167Total electrolytic excretion of potassium in urine of dogs after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID587131Inhibition of human carbonic anhydrase 2 after 15 mins by CO2 hydrase assay at pH 7.52011Bioorganic & medicinal chemistry, Mar-15, Volume: 19, Issue:6
Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.
AID1660461Diuretic activity in normotensive Wistar rat assessed as increase in urinary chloride excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID180389Diuretic activity by measuring the urinary output after 2 hr at the dose of 1 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1660497Renal protective activity in spontaneous hypertensive Wistar rat assessed as reduction in hypertension-induced glomerular size at 10 mg/kg, po administered via gavage for 7 days by hematoxylin and eosin staining based microscopic analysis2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID24420Partition coefficient (logP)1998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID16949Total electrolytic excretion of chlorine in urine of rats after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1434427Inhibition of recombinant human carbonic anhydrase 1 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 sec by Line-Weaver Burk plot analysis
AID16849Mean potassium excretion in rats when compound administered at 40 mg/kg po and vehicle dosed at 134.35 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID190869Compound was tested for urinary volume excretion in conscious rat at the dose of 30 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID190854Diuretic activity given as urinary output of 30 mg/kg perorally administered compound in rats1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID57184Compound was evaluated for diuretic activity, in female mongrel dogs by measuring amount of Cl- in urine after iv administration of 5 mg/kg (control/compound treatment results) Control = 51984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID156202Binding to POPC (palmitoyl-oleolyl-phosphatidyl-choline) liposomes using biosensor system2000Journal of medicinal chemistry, Jun-01, Volume: 43, Issue:11
SPR biosensor studies of the direct interaction between 27 drugs and a liposome surface: correlation with fraction absorbed in humans.
AID1079948Times to onset, minimal and maximal, observed in the indexed observations. [column 'DELAI' in source]
AID725955Inhibition of human recombinant carbonic anhydrase 1 by stopped flow CO2 hydration assay2013Journal of medicinal chemistry, Feb-28, Volume: 56, Issue:4
Cloning, characterization, and sulfonamide and thiol inhibition studies of an α-carbonic anhydrase from Trypanosoma cruzi, the causative agent of Chagas disease.
AID13951Oral diuretic activity was evaluated by measuring K+ excretion in dog at 5 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID185744Mean arterial pressure was measured in hypertensive rat at dose of 20 mg/kg, ip1981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID1287519Inhibition of Vibrio cholerae beta carbonic anhydrase incubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Apr-01, Volume: 26, Issue:7
Sulfonamide inhibition studies of the β-carbonic anhydrase from the newly discovered bacterium Enterobacter sp. B13.
AID51747Compound was evaluated for diuretic activity in chimpanzee measured as increase in volume of urine at 5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID15711Calculated partition coefficient (clogP)1998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID17555Total electrolytic excretion of sodium in urine of rats after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID57327Compound was evaluated for diuretic activity, in female mongrel dogs by measuring amount of Na+ in urine after iv administration of 5 mg/kg (control/compound treatment results) Control = 591984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID625284Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatic failure2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID180571Total Cl- milliequivalents excretion in diuretic test at the dose of 9 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1190063Inhibition of human recombinant carbonic anhydrase 1 by stopped-flow CO2 hydration assay2015Bioorganic & medicinal chemistry, Feb-01, Volume: 23, Issue:3
Sulfonamide inhibition studies of the η-class carbonic anhydrase from the malaria pathogen Plasmodium falciparum.
AID19865Mean excretion of chloride in conscious rats at a dose of 3.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1268964Inhibition of recombinant Sulfurihydrogenibium yellowstonense YO3AOP1 carbonic anhydrase by stopped flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, Jan-15, Volume: 26, Issue:2
Sulfonamide inhibition studies of the α-carbonic anhydrase from the gammaproteobacterium Thiomicrospira crunogena XCL-2, TcruCA.
AID180587Total Na+ milliequivalents excretion in diuretic test at the dose of 27 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID496819Antimicrobial activity against Plasmodium falciparum2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID190866Compound was tested for urinary volume excretion in conscious rat at the dose of 100 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1149924Natriuretic activity in Charles River rat assessed as sodium level in urine per cage collected 0.5 hrs interval at 9 mg/kg, po1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID16073Mean Chlorine excretion in rats when compound administered at 40 mg/kg po and vehicle dosed at 134.35 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1079947Comments (NB not yet translated). [column 'COMMENTAIRES' in source]
AID1091958Hydrophobicity, log P of the compound in octanol-water by shaking-flask method2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID16938Mean urine volume excretion in conscious rats at a dose of 30 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1149926Natriuretic activity in Charles River rat assessed as sodium level in urine per cage collected 0.5 hrs interval at 81 mg/kg, po1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID1142834Inhibition of human carbonic anhydrase-2 by stopped-flow CO2 hydration assay2014Bioorganic & medicinal chemistry, Jun-01, Volume: 22, Issue:11
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila.
AID1627600Antihypertensive activity in spontaneously hypertensive rat assessed as reduction in systolic blood pressure at 25 mg/kg via oral gavage qd administered for 4 days measured on day 4 by telemetry (Rvb = 2.5 +/- 2.2 mmHg)2016ACS medicinal chemistry letters, Jul-14, Volume: 7, Issue:7
Discovery of MK-7145, an Oral Small Molecule ROMK Inhibitor for the Treatment of Hypertension and Heart Failure.
AID1278409Inhibition of human carbonic anhydrase 2 preincubated for 15 mins by CO2 hydrase stopped flow assay2016Bioorganic & medicinal chemistry letters, Feb-15, Volume: 26, Issue:4
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea.
AID180600Compound was tested for the oral natriuretic activity in female rats at the dose 3 mg/kg; mequiv of Na+ x 100 / cage1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID186831Potassium salt excretion in conscious rat at the dose of 10 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1434429Inhibition of Burkholderia pseudomallei Gamma-carbonic anhydrase assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 sec by Line-Weaver Burk plot analysis
AID17359Total electrolytic excretion of potassium in urine of rats after peroral administration of 34.0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1660373Diuretic activity in normotensive Wistar rat assessed as urinary sodium excretion at 10 mg/kg, po administered via gavage after 8 hrs (Rvb = 61.82 to 80.81 mmol/L)2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID1190064Inhibition of human recombinant carbonic anhydrase 2 by stopped-flow CO2 hydration assay2015Bioorganic & medicinal chemistry, Feb-01, Volume: 23, Issue:3
Sulfonamide inhibition studies of the η-class carbonic anhydrase from the malaria pathogen Plasmodium falciparum.
AID91481Binding constant against human serum albumin (HSA)2001Journal of medicinal chemistry, Dec-06, Volume: 44, Issue:25
Cheminformatic models to predict binding affinities to human serum albumin.
AID176003The saluretic(Cl-) effect of compound was measured in rats after oral administration at 27 mg/kg dose; Cl-mequiv*100/cage=141981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID237474Percentage of drug bound in bovine plasma albumin2004Journal of medicinal chemistry, Jul-29, Volume: 47, Issue:16
Contribution of ionization and lipophilicity to drug binding to albumin: a preliminary step toward biodistribution prediction.
AID19862Mean excretion of chloride in conscious rats at a dose of 10 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID224547Compound was tested for diuretic activity in saline loaded mice, activity is expressed as the sodium present in urine as mean milli equivalent/kg per 5 hr at 64 mg/kg oral dose; ND denotes not determined1987Journal of medicinal chemistry, Dec, Volume: 30, Issue:12
[(6,7-Dichlorobenzo[b]thien-5-yl)oxy]acetic acids and 1,1-dioxides. 1. A structurally novel class of diuretics with hypotensive activity.
AID625286Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatitis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID180585Total Na+ milliequivalents excretion in diuretic test at the dose of 1 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1287518Inhibition of human carbonic anhydrase 2 incubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Apr-01, Volume: 26, Issue:7
Sulfonamide inhibition studies of the β-carbonic anhydrase from the newly discovered bacterium Enterobacter sp. B13.
AID780070Induction of diuresis in Sprague-Dawley rat at 25 mg/kg, po relative to vehicle-treated control2013Bioorganic & medicinal chemistry letters, Nov-01, Volume: 23, Issue:21
Discovery of a novel sub-class of ROMK channel inhibitors typified by 5-(2-(4-(2-(4-(1H-Tetrazol-1-yl)phenyl)acetyl)piperazin-1-yl)ethyl)isobenzofuran-1(3H)-one.
AID169987Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of K+x 100 / cage at 81 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID625282Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for cirrhosis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID168199Saluretic activity was evaluated for Na+ by flame photometry at 15 mg/kg perorally1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID1149925Natriuretic activity in Charles River rat assessed as sodium level in urine per cage collected 0.5 hrs interval at 27 mg/kg, po1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID625281Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for cholelithiasis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID467611Dissociation constant, pKa of the compound2009European journal of medicinal chemistry, Nov, Volume: 44, Issue:11
Prediction of volume of distribution values in human using immobilized artificial membrane partitioning coefficients, the fraction of compound ionized and plasma protein binding data.
AID1453411Inhibition of Burkholderia pseudomallei beta-carbonic anhydrase assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 secs by stopped-flow assay
AID1132618Natriuretic activity in rat assessed as per cage at 27 mg/kg, po1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID1660394Diuretic activity in normotensive Wistar rat assessed as urinary calcium excretion at 10 mg/kg, po administered via gavage after 8 hrs (Rvb = 5.93 to 6.87 mg/dl)2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID481441Aqueous diffusivity at 37C2010Journal of medicinal chemistry, May-13, Volume: 53, Issue:9
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
AID587132Inhibition of Leptonychotes weddellii alpha-carbonic anhydrase after 15 mins by CO2 hydrase assay at pH 7.52011Bioorganic & medicinal chemistry, Mar-15, Volume: 19, Issue:6
Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.
AID1278413Inhibition of recombinant Colwellia psychrerythraea gamma carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Feb-15, Volume: 26, Issue:4
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea.
AID180592Total Na+ milliequivalents excretion in diuretic test at the dose of 9 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID51593Compound was tested for the oral natriuretic activity in chimpanzee at the dose 5 mg/kg expressed as excretion rate in microequiv of Na+/min1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID15817Antidiuretic activity was determined expressed as Na+(sodium) excreted in milli equivalents was reported for a duration of 5 hours after administration of a dose of 100 mg/Kg1984Journal of medicinal chemistry, Dec, Volume: 27, Issue:12
N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as antihypertensive and diuretic agents.
AID169992Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Na+x 100 / cage at 9 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1473739Inhibition of human MRP2 overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-estradiol-17beta-D-glucuronide in presence of ATP and GSH measured after 20 mins by membrane vesicle transport assay2013Toxicological sciences : an official journal of the Society of Toxicology, Nov, Volume: 136, Issue:1
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
AID174282Compound was tested for antihypertensive activity in rat after 24 hr postdose1986Journal of medicinal chemistry, Jun, Volume: 29, Issue:6
Synthesis, saludiuretic, and antihypertensive activity of 6,7-disubstituted 1(2H)- and 3,4-dihydro-1(2H)-phthalazinones.
AID175532Diuretic activity by measuring the urinary output at the dose of 25 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID16069Mean Chlorine excretion in rats when compound administered at 20 mg/kg po and vehicle dosed at 67.18 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1079942Steatosis, proven histopathologically. Value is number of references indexed. [column 'STEAT' in source]
AID1194026Inhibition of recombinant Methanosarcina thermophila gamma-carbonic anhydrase by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry, Apr-15, Volume: 23, Issue:8
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune.
AID1434430Inhibition of Vibrio cholerae Gamma-carbonic anhydrase assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 sec by Line-Weaver Burk plot analysis
AID16065Mean Chlorine excretion in rats when compound administered at 2.5 mg/kg po and vehicle dosed at 8.4 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID17351Total electrolytic excretion of potassium in urine of rats after peroral administration of 3.40 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID19871Mean excretion of potassium in conscious rats at a dose of 3.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID168202Saluretic activity was evaluated for Na+ by flame photometry at 8 mg/kg perorally1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID169982Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Cl-x 100 / cage at 3 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID188267Sodium salt excretion in conscious rat at the dose of 3.0 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID21593Volume of urine 2 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1194025Inhibition of human recombinant carbonic anhydrase 2 by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry, Apr-15, Volume: 23, Issue:8
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune.
AID1079935Cytolytic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is > 5 (see ACUTE). Value is number of references indexed. [column 'CYTOL' in source]
AID57350Diuretic activity (ip) was tested in dogs;ND- Natriuresis and diuresis1990Journal of medicinal chemistry, Jun, Volume: 33, Issue:6
Angiotensin-converting enzyme inhibitors. 9. Novel [[N-(1-carboxy-3-phenylpropyl)amino]acyl]glycine derivatives with diuretic activity.
AID625290Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for liver fatty2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID27167Delta logD (logD6.5 - logD7.4)2000Journal of medicinal chemistry, Jun-29, Volume: 43, Issue:13
QSAR model for drug human oral bioavailability.
AID180602Compound was tested for the oral natriuretic activity in female rats at the dose 81 mg/kg; mequiv of Na+ x 100 / cage1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID62351Saluretic property in average of three anesthetized dogs after 5 mg/kg intravenous administration1983Journal of medicinal chemistry, Apr, Volume: 26, Issue:4
2-(Aminomethyl)phenols, a new class of saluretic agents. 5. Fused-ring analogues.
AID168198Saluretic activity was evaluated for K+ by flame photometry at 8 mg/kg perorally1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID57179Compound was evaluated for diuretic activity, administered orally in female mongrel dogs (5 mg/kg) measured as milliequivalents of Cl-1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID60630Maximum percent decrease in blood pressure at the dose of 100 mg/kg ip1990Journal of medicinal chemistry, Jun, Volume: 33, Issue:6
Angiotensin-converting enzyme inhibitors. 9. Novel [[N-(1-carboxy-3-phenylpropyl)amino]acyl]glycine derivatives with diuretic activity.
AID1660466Diuretic activity in normotensive Wistar rat assessed as increase in urinary potassium excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID612732Inhibition of Salmonella Typhimurium recombinant carbonic anhydrase 2 at pH 8.3 by stopped flow CO2 hydration assay2011Bioorganic & medicinal chemistry, Aug-15, Volume: 19, Issue:16
Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates.
AID780069Induction of natriuresis in Sprague-Dawley rat at 25 mg/kg, po relative to vehicle-treated control2013Bioorganic & medicinal chemistry letters, Nov-01, Volume: 23, Issue:21
Discovery of a novel sub-class of ROMK channel inhibitors typified by 5-(2-(4-(2-(4-(1H-Tetrazol-1-yl)phenyl)acetyl)piperazin-1-yl)ethyl)isobenzofuran-1(3H)-one.
AID190442Saluretic property after 50 mg/kg oral administration in rats1983Journal of medicinal chemistry, Apr, Volume: 26, Issue:4
2-(Aminomethyl)phenols, a new class of saluretic agents. 5. Fused-ring analogues.
AID496829Antimicrobial activity against Leishmania infantum2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID1061069Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by stopped flow CO2 hydration assay2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sulfonamide inhibition studies of the δ-carbonic anhydrase from the diatom Thalassiosira weissflogii.
AID1195369Inhibition of human carbonic anhydrase 1 pre-incubated for 15 mins by stopped-flow CO2 hydration assay2015Bioorganic & medicinal chemistry, May-15, Volume: 23, Issue:10
The β-carbonic anhydrase from the malaria mosquito Anopheles gambiae is highly inhibited by sulfonamides.
AID496824Antimicrobial activity against Toxoplasma gondii2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID16932Mean urine volume excretion in conscious rats at a dose of 0.3 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID16947Total electrolytic excretion of chlorine in urine of rats after peroral administration of 1.01 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID386623Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells at 100 uM by confocal microscopy2008Journal of medicinal chemistry, Oct-09, Volume: 51, Issue:19
Structural requirements for drug inhibition of the liver specific human organic cation transport protein 1.
AID17171Total electrolytic excretion of potassium in urine of rats after peroral administration of 0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID228205Compound was tested for urinary volume excretion in conscious rat at the dose of 1.0 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1726079Inhibition of Vibrio cholerae beta carbonic anhydrase pre-incubated for 15 mins prior to testing by phenol red-based stopped-flow CO2 hydration assay2020ACS medicinal chemistry letters, Nov-12, Volume: 11, Issue:11
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in
AID1660380Diuretic activity in normotensive Wistar rat assessed as urinary potassium excretion at 10 mg/kg, po administered via gavage after 8 hrs (Rvb = 22.39 to 24.21 mmol/L)2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID185745Mean arterial pressure was measured in hypertensive rat at dose of 20 mg/kg, po1981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID1061068Inhibition of Leishmania donovani chagasi recombinant beta-carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sulfonamide inhibition studies of the δ-carbonic anhydrase from the diatom Thalassiosira weissflogii.
AID186830Potassium salt excretion in conscious rat at the dose of 1.0 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1437001Antihypertensive activity in rat spontaneous hypertensive model assessed as change in systolic blood pressure at 25 mg/kg, po measured after 3 days2017Bioorganic & medicinal chemistry letters, 02-15, Volume: 27, Issue:4
The design and synthesis of novel spirocyclic heterocyclic sulfone ROMK inhibitors as diuretics.
AID22025Tested for the diuretic activity by measuring the urinary volume after peroral administering 0 uM/Kg of drug in rats1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID587130Inhibition of human carbonic anhydrase 1 after 15 mins by CO2 hydrase assay at pH 7.52011Bioorganic & medicinal chemistry, Mar-15, Volume: 19, Issue:6
Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.
AID13974Oral diuretic activity was evaluated by measuring Na+ excretion in Rat at 9 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID625292Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) combined score2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID51733Compound was evaluated for diuretic activity in chimpanzee measured as increase in the number of microequivalents of Na+ /min at 1 0.5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1628037Inhibition of human cytosolic carbonic anhydrase 2 preincubated for 15 mins by stop flow CO2 hydrase assay2016Bioorganic & medicinal chemistry letters, 09-01, Volume: 26, Issue:17
Cloning, expression, purification and sulfonamide inhibition profile of the complete domain of the η-carbonic anhydrase from Plasmodium falciparum.
AID1453412Inhibition of human carbonic anhydrase-1 assessed as reduction in CO2 hydration preincubated for 15 mins followed by CO2 addition measured for 10 to 100 secs by stopped-flow assay
AID476929Human intestinal absorption in po dosed human2010European journal of medicinal chemistry, Mar, Volume: 45, Issue:3
Neural computational prediction of oral drug absorption based on CODES 2D descriptors.
AID188266Sodium salt excretion in conscious rat at the dose of 100 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1660463Diuretic activity in spontaneous hypertensive Wistar rat assessed as increase in urinary sodium excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID453203Lipophilicity, log D of the compound2010Bioorganic & medicinal chemistry letters, Jan-01, Volume: 20, Issue:1
Development of an in silico model for human skin permeation based on a Franz cell skin permeability assay.
AID186698Compound was tested for blood pressure change in rats after oral administration of 50 mg/kg dose after 4 hours1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1660465Diuretic activity in spontaneous hypertensive Wistar rat assessed as decrease in urinary calcium excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID1660503Anti-urolithic activity in spontaneous hypertensive Wistar rats assessed as reduction in CaOx crystal formation in cumulative urine at 10 mg/kg, po administered via gavage in presence of sodium oxalate by Neubauer counting chamber method relative to contr2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID15980Antidiuretic activity was determined in SH rats expressed as K(+) (potassium) excreted in milli equivalents was reported for a duration of 5 hours after administration of a dose of 100 mg/Kg.1984Journal of medicinal chemistry, Dec, Volume: 27, Issue:12
N2-(4-Substituted-2,6-dichlorophenyl)-N1,N1-dimethylformamidines as antihypertensive and diuretic agents.
AID1262267Inhibition of Chionodraco hamatus alphaCA incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID1149933Diuretic activity in dog assessed as chloride level in urine collected for 2 hrs at 5 mg/kg, iv over a period of 5 mins (Rvb = 1 to 10 microEq)1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID16057Mean Chlorine excretion in rats when compound administered at 10 mg/kg po and vehicle dosed at 33.59 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID193276Hypotensive activity was determined in Spontaneously hypertensive rats (SHR) and initial blood pressure was determined at 50 mg/kg oral dose1987Journal of medicinal chemistry, Dec, Volume: 30, Issue:12
[(6,7-Dichlorobenzo[b]thien-5-yl)oxy]acetic acids and 1,1-dioxides. 1. A structurally novel class of diuretics with hypotensive activity.
AID169984Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Cl-x 100 / cage at 9 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID190863Compound was tested for urinary volume excretion in conscious rat at the dose of 0.3 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID186697Compound was tested for blood pressure change in rats after oral administration of 50 mg/kg dose after 24 hours1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID625279Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for bilirubinemia2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID17542Total electrolytic excretion of sodium in urine of dogs after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID180577Total K+ milliequivalents excretion in diuretic test at the dose of 27 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID16002Evaluated for salidiuretic activity measured as sodium ion excretion in Rat, administered orally at a dose of 16.5 mg/kg1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1079941Liver damage due to vascular disease: peliosis hepatitis, hepatic veno-occlusive disease, Budd-Chiari syndrome. Value is number of references indexed. [column 'VASC' in source]
AID1240216Inhibition of Methanosarcina thermophila recombinant gamma carbonic anhydrase by stopped flow CO2 hydrase assay method2015Bioorganic & medicinal chemistry letters, Sep-01, Volume: 25, Issue:17
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Pseudoalteromonas haloplanktis.
AID173776Dose required to produce an excretion of 2 mequiv of Na+/kg bw/6h vs control groups1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID453204Permeability in human skin after 48 hrs by Franz cell permeability assay2010Bioorganic & medicinal chemistry letters, Jan-01, Volume: 20, Issue:1
Development of an in silico model for human skin permeation based on a Franz cell skin permeability assay.
AID186861Maximum fall in mean arterial blood pressure was measured in SH rats when compound was administered at 40 mg/kg perorally1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID588210Human drug-induced liver injury (DILI) modelling dataset from Ekins et al2010Drug metabolism and disposition: the biological fate of chemicals, Dec, Volume: 38, Issue:12
A predictive ligand-based Bayesian model for human drug-induced liver injury.
AID16077Mean Chlorine excretion in rats when compound administered at 5 mg/kg po and vehicle dosed at 16.79 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1132616Natriuretic activity in rat assessed as per cage at 3 mg/kg, po1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID21820Mean urinary output in rats when compound administered at 40 mg/kg po and vehicle dosed at 134.35 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID644381Inhibition of human recombinant carbonic anhydrase 2 after 15 mins by stopped flow CO2 hydration assay2012Bioorganic & medicinal chemistry, Feb-15, Volume: 20, Issue:4
Cloning, characterization and sulfonamide inhibition studies of an α-carbonic anhydrase from the living fossil sponge Astrosclera willeyana.
AID57181Compound was evaluated for diuretic activity, administered orally in female mongrel dogs (5 mg/kg) measured as milliequivalents of Na1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID496827Antimicrobial activity against Leishmania amazonensis2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID1142838Inhibition of Helicobacter pylori carbonic anhydrase by stopped-flow CO2 hydration assay2014Bioorganic & medicinal chemistry, Jun-01, Volume: 22, Issue:11
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila.
AID174283Compound was tested for antihypertensive activity in rat after 4 hr postdose1986Journal of medicinal chemistry, Jun, Volume: 29, Issue:6
Synthesis, saludiuretic, and antihypertensive activity of 6,7-disubstituted 1(2H)- and 3,4-dihydro-1(2H)-phthalazinones.
AID169981Compound was evaluated for diuretic activity administered orally in female rats measured as milliequivalents of Cl-+x 100 / cage at 27 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1275913Inhibition of human Carbonic anhydrase1 using CO2 as substrate preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry, Mar-01, Volume: 24, Issue:5
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID218756Compound was tested for diuretic activity in dogs at 5 mg/kg dose after intravenous administration measured as microequivalent of Na+/minute; 12/166 (Control/Drug treated)1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID743512Inhibition of Sulfurihydrogenibium yellowstonense YO3AOP1 recombinant carbonic anhydrase preincubated for 15 mins by CO2 hydration stopped-flow assay2013Bioorganic & medicinal chemistry, Mar-15, Volume: 21, Issue:6
The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides.
AID29845Estimation of fraction absorbed (Fa) in the human intestine using biosensor technology.2000Journal of medicinal chemistry, Jun-01, Volume: 43, Issue:11
SPR biosensor studies of the direct interaction between 27 drugs and a liposome surface: correlation with fraction absorbed in humans.
AID51746Compound was evaluated for diuretic activity in chimpanzee measured as increase in volume of urine at 1 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID51589Compound was tested for the oral diuretic activity in chimpanzee at the dose 5 mg/kg expressed as excretion rate in microequiv of K+/min1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID168195Saluretic activity was evaluated for K+ by flame photometry at 15 mg/kg perorally1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID467613Volume of distribution at steady state in human2009European journal of medicinal chemistry, Nov, Volume: 44, Issue:11
Prediction of volume of distribution values in human using immobilized artificial membrane partitioning coefficients, the fraction of compound ionized and plasma protein binding data.
AID496828Antimicrobial activity against Leishmania donovani2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID1240214Inhibition of Nostoc commune gamma carbonic anhydrase by CO2 hydration assay2015Bioorganic & medicinal chemistry letters, Sep-01, Volume: 25, Issue:17
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Pseudoalteromonas haloplanktis.
AID1149934Diuretic activity in dog assessed as urine volume collected for 2 hrs at 5 mg/kg, iv over a period of 5 mins (Rvb = 1 to 2 mL)1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID17332Na+ excretion mequiv/kg in saline-loaded mice administered at a dose 0.3 ml/kg perorally1984Journal of medicinal chemistry, Aug, Volume: 27, Issue:8
Substituted 5,6-dihydrofuro[3,2-f]-1,2-benzisoxazole-6-carboxylic acids: high-ceiling diuretics with uricosuric activity.
AID711214Inhibition of human recombinant carbonic anhydrase 1 preincubated for 15 mins by stopped-flow CO2 hydrase assay2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
DNA cloning, characterization, and inhibition studies of an α-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID190865Compound was tested for urinary volume excretion in conscious rat at the dose of 10 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID1240215Inhibition of Pseudoalteromonas haloplanktis gamma carbonic anhydrase by CO2 hydration assay2015Bioorganic & medicinal chemistry letters, Sep-01, Volume: 25, Issue:17
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Pseudoalteromonas haloplanktis.
AID168196Saluretic activity was evaluated for K+ by flame photometry at 30 mg/kg perorally1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID190857Diuretic activity given as urinary output of 8 mg/kg perorally administered compound in rats1993Journal of medicinal chemistry, Jan-08, Volume: 36, Issue:1
o-Chlorobenzenesulfonamidic derivatives of (aryloxy)propanolamines as beta-blocking/diuretic agents.
AID1149932Diuretic activity in dog assessed as potassium level in urine collected for 2 hrs at 5 mg/kg, iv over a period of 5 mins (Rvb = 5 to 30 microEq)1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID13793Oral diuretic activity was evaluated by measuring K+ excretion in dog at 0.3 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1647955prevention of heart failure in verapamil treated zebrafish AB assessed as efficacy on blood flow velocity at 0.5 ug/ml preincubated for 4.5 hrs followed by verapamil treatment and measured after 30 mins relative to verapamil alone
AID16946Total electrolytic excretion of chlorine in urine of rats after peroral administration of 0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID496821Antimicrobial activity against Leishmania2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID1132622Natriuretic activity in chimpanzee assessed as change in Curate to Cinsulin ratio at 5 mg/kg, po1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID17552Total electrolytic excretion of sodium in urine of rats after peroral administration of 0 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1079937Severe hepatitis, defined as possibly life-threatening liver failure or through clinical observations. Value is number of references indexed. [column 'MASS' in source]
AID1473741Inhibition of human MRP4 overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-estradiol-17beta-D-glucuronide in presence of ATP and GSH measured after 20 mins by membrane vesicle transport assay2013Toxicological sciences : an official journal of the Society of Toxicology, Nov, Volume: 136, Issue:1
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
AID1262264Inhibition of human CA2 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay2015Bioorganic & medicinal chemistry letters, Dec-01, Volume: 25, Issue:23
Anion and sulfonamide inhibition studies of an α-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.
AID1627544Kaliuretic activity in Sprague-Dawley rat administered via oral gavage 30 mins prior to void induction by loading saline measured upto 4 hrs relative to vehicle treated control2016ACS medicinal chemistry letters, Jul-14, Volume: 7, Issue:7
Discovery of MK-7145, an Oral Small Molecule ROMK Inhibitor for the Treatment of Hypertension and Heart Failure.
AID496830Antimicrobial activity against Leishmania major2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID19873Mean excretion of sodium in conscious rats at a dose of 0.3 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1079932Highest frequency of moderate liver toxicity observed during clinical trials, expressed as a percentage. [column '% BIOL' in source]
AID21572Urinary sodium 1 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID230296Ratio of Total electrolytic excretion of sodium and potassium in urine of rats after peroral administration of 1.01 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1079938Chronic liver disease either proven histopathologically, or through a chonic elevation of serum amino-transferase activity after 6 months. Value is number of references indexed. [column 'CHRON' in source]
AID521220Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay2007Nature chemical biology, May, Volume: 3, Issue:5
Chemical genetics reveals a complex functional ground state of neural stem cells.
AID1660359Diuretic activity in normotensive Wistar rat assessed as urine pH at 10 mg/kg, po administered via gavage after 8 hrs (Rvb = 6.14 to 6.21 No_unit)2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID22056Tested for the diuretic activity by measuring the urinary volume after peroral administering 3.40 uM/Kg of drug in rats1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1091955Dissociation constant, pKa of the compound at pH 7.32011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID409954Inhibition of mouse brain MAOA2008Journal of medicinal chemistry, Nov-13, Volume: 51, Issue:21
Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.
AID16588Oral diuretic activity was evaluated by measuring Cl- excretion in dog at 0.3 mg/kg after ip administration (0-6 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID1244134Induction of kaliuresis in Sprague-Dawley rat at 25 mg/kg, po after 4 hrs relative to control2015ACS medicinal chemistry letters, Jul-09, Volume: 6, Issue:7
Discovery of a Potent and Selective ROMK Inhibitor with Pharmacokinetic Properties Suitable for Preclinical Evaluation.
AID186833Potassium salt excretion in conscious rat at the dose of 3.0 mg/kg expressed as urinary excretion in treated rats/urinary excretion in control rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID218754Compound was tested for diuretic activity in dogs at 5 mg/kg dose after intravenous administration measured as microequivalent of Cl-/minute; 5/156 (Control/Drug treated)1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID175816Diuretic activity in rats1986Journal of medicinal chemistry, Aug, Volume: 29, Issue:8
Pyrimidinones. 3. N-substituted 6-phenylpyrimidinones and pyrimidinediones with diuretic/hypotensive and antiinflammatory activity.
AID24185Distribution coefficient in octanol/water at pH 7.41998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID21816Mean urinary output in rats when compound administered at 20 mg/kg po and vehicle dosed at 67.18 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID194007Hypotensive activity was determined in Spontaneously hypertensive rats (SHR) and peak decrease in systolic blood pressure on third day,2h post administration of 50 mg/kg oral dose was determined1987Journal of medicinal chemistry, Dec, Volume: 30, Issue:12
[(6,7-Dichlorobenzo[b]thien-5-yl)oxy]acetic acids and 1,1-dioxides. 1. A structurally novel class of diuretics with hypotensive activity.
AID17315Mean sodium excretion in rats when compound administered at 5 mg/kg po and vehicle dosed at 16.79 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID16689Mean potassium excretion in rats when compound administered at 0 mg/kg po and vehicle dosed at 0 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1149923Natriuretic activity in Charles River rat assessed as sodium level in urine per cage collected 0.5 hrs interval at 3 mg/kg, po1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID481444Octanol-water partition coefficient, log P of the compound2010Journal of medicinal chemistry, May-13, Volume: 53, Issue:9
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
AID1188137Inhibition of Porphyromonas gingivalis Beta-carbonic anhydrase compound preincubated for 15 mins by stopped flow CO2 hydrase assay method2014Bioorganic & medicinal chemistry, Sep-01, Volume: 22, Issue:17
Sulfonamide inhibition study of the carbonic anhydrases from the bacterial pathogen Porphyromonas gingivalis: the β-class (PgiCAb) versus the γ-class (PgiCA) enzymes.
AID496820Antimicrobial activity against Trypanosoma brucei2010Bioorganic & medicinal chemistry, Mar-15, Volume: 18, Issue:6
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
AID129601Acute toxicity in mice when given po1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1278410Inhibition of Porphyromonas gingivalis gamma carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Feb-15, Volume: 26, Issue:4
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea.
AID1647953prevention of heart failure in verapamil treated zebrafish AB assessed as efficacy on cardiac output at 0.5 ug/ml preincubated for 4.5 hrs followed by verapamil treatment and measured after 30 mins relative to verapamil alone
AID19877Mean excretion of sodium in conscious rats at a dose of 3.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1808089Stability of compound in mini gut model assessed as half life by LC-MS analysis2021Journal of medicinal chemistry, 12-09, Volume: 64, Issue:23
Searching for New Microbiome-Targeted Therapeutics through a Drug Repurposing Approach.
AID17553Total electrolytic excretion of sodium in urine of rats after peroral administration of 1.01 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID16937Mean urine volume excretion in conscious rats at a dose of 3.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID185810Initial blood pressure before treatment1987Journal of medicinal chemistry, Dec, Volume: 30, Issue:12
[(6,7-Dichlorobenzo[b]thien-5-yl)oxy]acetic acids and 1,1-dioxides. 1. A structurally novel class of diuretics with hypotensive activity.
AID1061169Inhibition of recombinant Methanosarcina thermophila gamma-CA CAM by stopped flow CO2 hydration assay2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the oral pathogen Porphyromonas gingivalis.
AID180392Diuretic activity by measuring the urinary output after 2 hr at the dose of 3 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID168636Compound was tested for oral salidiuretic activity (control/drug treatment value) in rats expressed in Na+, mequiv/6 hr at a dose of 110 mg/kg; 0.261/0.7351986Journal of medicinal chemistry, Jan, Volume: 29, Issue:1
[p-[(Thienylcarbonyl)amino]phenoxy]propanolamines derivatives as diuretic and beta-adrenergic receptor blocking agents.
AID16853Mean potassium excretion in rats when compound administered at 5 mg/kg po and vehicle dosed at 16.79 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID175997Saluretic(Na+) effect of compound was measured in rats after oral administration at 3 mg/kg dose; Na+ mequiv*100/cage1981Journal of medicinal chemistry, Jan, Volume: 24, Issue:1
2-(Aminomethyl)phenols, a new class of saluretic agents. 2. Synthesis and pharmacological properties of the 5-aza isostere of 2-(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenol.
AID481439Absolute bioavailability in human2010Journal of medicinal chemistry, May-13, Volume: 53, Issue:9
How well can the Caco-2/Madin-Darby canine kidney models predict effective human jejunal permeability?
AID17174Total electrolytic excretion of potassium in urine of rats after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID19872Mean excretion of potassium in conscious rats at a dose of 30 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID311524Oral bioavailability in human2007Bioorganic & medicinal chemistry, Dec-15, Volume: 15, Issue:24
Hologram QSAR model for the prediction of human oral bioavailability.
AID21774volume of urine at 81 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID21581Urinary sodium 4 hr after the compound was administered 10 mg/kg po in rat1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1132621Natriuretic activity in chimpanzee assessed as per min at 5 mg/kg, po1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
(Acylaryloxy)acetic acid diuretics. 2. (2-Alkyl-2-aryl-1-oxo-5-indanyloxy)acetic acids.
AID51753Compound was evaluated for diuretic activity in chimpanzee measured as clearance of insulin and urate after intra venous administration of.1 5 mg/kg. 1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID625280Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for cholecystitis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID176936Dose required to produce increase in 50 % in urine production vs control groups1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID173966Dose required to produce increase in 200 % in urine production vs control groups; Not determined1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID62235Compound was tested for the saluretic property in dogs after intravenous administration of 5 mg/kg; 100-249 micro equivalents of Na+ excreted per minute1981Journal of medicinal chemistry, Sep, Volume: 24, Issue:9
2-(Aminomethyl)phenols, a new class of saluretic agents. 3. Effects of functional group reorientation and modification.
AID725956Inhibition of human recombinant carbonic anhydrase 2 by stopped flow CO2 hydration assay2013Journal of medicinal chemistry, Feb-28, Volume: 56, Issue:4
Cloning, characterization, and sulfonamide and thiol inhibition studies of an α-carbonic anhydrase from Trypanosoma cruzi, the causative agent of Chagas disease.
AID1473738Inhibition of human BSEP overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-taurocholate in presence of ATP measured after 15 to 20 mins by membrane vesicle transport assay2013Toxicological sciences : an official journal of the Society of Toxicology, Nov, Volume: 136, Issue:1
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
AID625287Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatomegaly2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID196141Natriuretic activity in rats at 81 mg/kg of dosage; mequiv of Na1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 3. 2,3-Dihydro-5-acyl-2-benzofurancarboxylic acids, a new class of uricosuric diuretics.
AID17311Mean sodium excretion in rats when compound administered at 40 mg/kg po and vehicle dosed at 134.35 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID1278412Inhibition of Pseudoalteromonas haloplanktis gamma carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Feb-15, Volume: 26, Issue:4
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea.
AID16571Oral diuretic activity was evaluated by measuring Cl- excretion in Rat at 3 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID21828Mean urinary output in rats when compound administered at 80 mg/kg po and vehicle dosed at 268.71 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID17295Mean sodium excretion in rats when compound administered at 10 mg/kg po and vehicle dosed at 33.59 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID24183Distribution coefficient in octanol/water at pH 5.51998Journal of medicinal chemistry, Dec-03, Volume: 41, Issue:25
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach.
AID51761Compound was evaluated for diuretic activity in chimpanzee measured as increase in the number of microequivalents of K+ /min at 5 mg/kg1984Journal of medicinal chemistry, Jul, Volume: 27, Issue:7
(Acylaryloxy)acetic acid diuretics. 5. [(2-Alkyl- and 2,2-disubstituted-1,3-dioxo-5-indanyl)oxy]acetic acids.
AID1291363Inhibition of recombinant Vibrio cholerae gamma-carbonic anhydrase preincubated for 15 mins by stopped-flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Apr-15, Volume: 26, Issue:8
Comparison of the sulfonamide inhibition profiles of the α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae.
AID17284Mean sodium excretion in rats (Control/Drug treatment value); value 0.43/2.861992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID180582Total K+ milliequivalents excretion in diuretic test at the dose of 9 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID16934Mean urine volume excretion in conscious rats at a dose of 1.0 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1660492In vivo antioxidant activity in Wistar rat model of hypertension-induced oxidative stress assessed as reduction in nitrite level in renal tissue at 10 mg/kg, po administered via gavage for 7 days by Griess reagent based assay2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID232279Compound was tested for the ratio of clearance of urate to clearance of inulin levels at 5 mg/kg in Chimpanzee1981Journal of medicinal chemistry, Jul, Volume: 24, Issue:7
(Acylaryloxy)acetic acid diuretics. 4. Indeno[5,4-b]furan-2-carboxylic acids.
AID16857Mean potassium excretion in rats when compound administered at 80 mg/kg po and vehicle dosed at 268.71 umol/kg1992Journal of medicinal chemistry, Oct-30, Volume: 35, Issue:22
N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics.
AID239884pKa value of the compound2004Journal of medicinal chemistry, Jul-29, Volume: 47, Issue:16
Contribution of ionization and lipophilicity to drug binding to albumin: a preliminary step toward biodistribution prediction.
AID16796Total electrolytic excretion of chlorine in urine of dogs after peroral administration of 10.1 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID16006Compound administered orally at a dose of 81 mg/kg was evaluated for salidiuretic activity measured as sodium ion excretion in Rat1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID180394Diuretic activity by measuring the urinary output after 2 hr at the dose of 9 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1079936Choleostatic liver toxicity, either proven histopathologically or where the ratio of maximal ALT or AST activity above normal to that of Alkaline Phosphatase is < 2 (see ACUTE). Value is number of references indexed. [column 'CHOLE' in source]
AID1142837Inhibition of Legionella pneumophilia subsp. Pneumophila strain Philadelphia-1 carbonic anhydrase-2 assessed as CO2 hydrase activity by stopped-flow assay2014Bioorganic & medicinal chemistry, Jun-01, Volume: 22, Issue:11
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila.
AID19876Mean excretion of sodium in conscious rats at a dose of 100 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID711213Inhibition of human recombinant carbonic anhydrase 2 preincubated for 15 mins by stopped-flow CO2 hydrase assay2012Journal of medicinal chemistry, Dec-13, Volume: 55, Issue:23
DNA cloning, characterization, and inhibition studies of an α-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.
AID13957Oral diuretic activity was evaluated by measuring Na+ excretion in Rat at 27 mg/kg after ip administration (0-5 hr)1980Journal of medicinal chemistry, Dec, Volume: 23, Issue:12
2-(Aminomethyl)phenols, a new class of saluretic agents. 1. Effects of nuclear substitution.
AID19878Mean excretion of sodium in conscious rats at a dose of 30 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID1808090Stability in human gut microbes assessed as half life by LC-MS analysis2021Journal of medicinal chemistry, 12-09, Volume: 64, Issue:23
Searching for New Microbiome-Targeted Therapeutics through a Drug Repurposing Approach.
AID1278411Inhibition of Nostoc commune gamma carbonic anhydrase preincubated for 15 mins by stopped flow CO2 hydration assay2016Bioorganic & medicinal chemistry letters, Feb-15, Volume: 26, Issue:4
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea.
AID19867Mean excretion of potassium in conscious rats at a dose of 0.3 mg/kg given orally1989Journal of medicinal chemistry, Jun, Volume: 32, Issue:6
1-(2-aminoethyl)-6-aryl-4H- [1,2,4]triazolo[4,3-a][1,4]benzodiazepines with diuretic and natriuretic activity.
AID180575Total K+ milliequivalents excretion in diuretic test at the dose of 1 mg/kg1982Journal of medicinal chemistry, Jan, Volume: 25, Issue:1
Syntheses and diuretic activity of 1,2-dihydro-2-(3-pyridyl)-3H-pyrido[2,3-d]pyrimidin-4-one and related compounds.
AID1660464Diuretic activity in spontaneous hypertensive Wistar rat assessed as increase in urinary chloride excretion at 10 mg/kg, po administered via gavage for 7 days2020Journal of natural products, 06-26, Volume: 83, Issue:6
Diuretic and Renal Protective Effect of Kaempferol 3-
AID1149931Diuretic activity in dog assessed as sodium level in urine collected for 2 hrs at 5 mg/kg, iv over a period of 5 mins (Rvb = 5 to 30 microEq)1977Journal of medicinal chemistry, Nov, Volume: 20, Issue:11
(Acylaryloxy)acetic acid diuretics. 1. (2-Alkyl- and 2,2-dialkyl-1-oxo-5-indanyloxy)acetic acids.
AID17172Total electrolytic excretion of potassium in urine of rats after peroral administration of 1.01 uM/Kg of drug1994Journal of medicinal chemistry, Oct-28, Volume: 37, Issue:22
Synthesis and diuretic activity of alkyl- and arylguanidine analogs of N,N'-dicyclohexyl-4-morpholinecarboxamidine in rats and dogs.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID504749qHTS profiling for inhibitors of Plasmodium falciparum proliferation2011Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets.
AID1347057CD47-SIRPalpha protein protein interaction - LANCE assay qHTS validation2019PloS one, , Volume: 14, Issue:7
Quantitative high-throughput screening assays for the discovery and development of SIRPα-CD47 interaction inhibitors.
AID1347049Natriuretic polypeptide receptor (hNpr1) antagonism - Pilot screen2019Science translational medicine, 07-10, Volume: 11, Issue:500
Inhibition of natriuretic peptide receptor 1 reduces itch in mice.
AID1347410qHTS for inhibitors of adenylyl cyclases using a fission yeast platform: a pilot screen against the NCATS LOPAC library2019Cellular signalling, 08, Volume: 60A fission yeast platform for heterologous expression of mammalian adenylyl cyclases and high throughput screening.
AID588378qHTS for Inhibitors of ATXN expression: Validation
AID1347405qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS LOPAC collection2020ACS chemical biology, 07-17, Volume: 15, Issue:7
High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle.
AID504836Inducers of the Endoplasmic Reticulum Stress Response (ERSR) in human glioma: Validation2002The Journal of biological chemistry, Apr-19, Volume: 277, Issue:16
Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347058CD47-SIRPalpha protein protein interaction - HTRF assay qHTS validation2019PloS one, , Volume: 14, Issue:7
Quantitative high-throughput screening assays for the discovery and development of SIRPα-CD47 interaction inhibitors.
AID1347151Optimization of GU AMC qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1508630Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay2021Cell reports, 04-27, Volume: 35, Issue:4
A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome.
AID1347050Natriuretic polypeptide receptor (hNpr2) antagonism - Pilot subtype selectivity assay2019Science translational medicine, 07-10, Volume: 11, Issue:500
Inhibition of natriuretic peptide receptor 1 reduces itch in mice.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347045Natriuretic polypeptide receptor (hNpr1) antagonism - Pilot counterscreen GloSensor control cell line2019Science translational medicine, 07-10, Volume: 11, Issue:500
Inhibition of natriuretic peptide receptor 1 reduces itch in mice.
AID588349qHTS for Inhibitors of ATXN expression: Validation of Cytotoxic Assay
AID1347059CD47-SIRPalpha protein protein interaction - Alpha assay qHTS validation2019PloS one, , Volume: 14, Issue:7
Quantitative high-throughput screening assays for the discovery and development of SIRPα-CD47 interaction inhibitors.
AID1347411qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Mechanism Interrogation Plate v5.0 (MIPE) Libary2020ACS chemical biology, 07-17, Volume: 15, Issue:7
High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle.
AID1745854NCATS anti-infectives library activity on HEK293 viability as a counter-qHTS vs the C. elegans viability qHTS2023Disease models & mechanisms, 03-01, Volume: 16, Issue:3
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
AID1745855NCATS anti-infectives library activity on the primary C. elegans qHTS viability assay2023Disease models & mechanisms, 03-01, Volume: 16, Issue:3
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID1347100qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347104qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347407qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Pharmaceutical Collection2020ACS chemical biology, 07-17, Volume: 15, Issue:7
High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle.
AID1347096qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for U-2 OS cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347424RapidFire Mass Spectrometry qHTS Assay for Modulators of WT P53-Induced Phosphatase 1 (WIP1)2019The Journal of biological chemistry, 11-15, Volume: 294, Issue:46
Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens.
AID1347099qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347154Primary screen GU AMC qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347095qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347094qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347090qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347097qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347108qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347091qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347101qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347107qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh30 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347105qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347089qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347093qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347102qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347098qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347103qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347106qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for control Hh wild type fibroblast cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347425Rhodamine-PBP qHTS Assay for Modulators of WT P53-Induced Phosphatase 1 (WIP1)2019The Journal of biological chemistry, 11-15, Volume: 294, Issue:46
Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens.
AID1347092qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1798598CA Inhibition Assay from Article 10.1016/j.bmcl.2008.03.051: \\Carbonic anhydrase inhibitors. Interaction of indapamide and related diuretics with 12 mammalian isozymes and X-ray crystallographic studies for the indapamide-isozyme II adduct.\\2008Bioorganic & medicinal chemistry letters, Apr-15, Volume: 18, Issue:8
Carbonic anhydrase inhibitors. Interaction of indapamide and related diuretics with 12 mammalian isozymes and X-ray crystallographic studies for the indapamide-isozyme II adduct.
AID1796991Carbonic Anhydrase Enzyme Inhibition Assay from Article 10.1021/jm011112j: \\Successful virtual screening for novel inhibitors of human carbonic anhydrase: strategy and experimental confirmation.\\2002Journal of medicinal chemistry, Aug-15, Volume: 45, Issue:17
Successful virtual screening for novel inhibitors of human carbonic anhydrase: strategy and experimental confirmation.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
AID1224864HCS microscopy assay (F508del-CFTR)2016PloS one, , Volume: 11, Issue:10
Increasing the Endoplasmic Reticulum Pool of the F508del Allele of the Cystic Fibrosis Transmembrane Conductance Regulator Leads to Greater Folding Correction by Small Molecule Therapeutics.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6,441)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903201 (49.70)18.7374
1990's914 (14.19)18.2507
2000's936 (14.53)29.6817
2010's1150 (17.85)24.3611
2020's240 (3.73)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 124.98

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index124.98 (24.57)
Research Supply Index9.11 (2.92)
Research Growth Index4.47 (4.65)
Search Engine Demand Index238.65 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (124.98)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Trials2,165 (31.28%)5.53%
Reviews0 (0.00%)6.00%
Reviews317 (4.58%)6.00%
Case Studies0 (0.00%)4.05%
Case Studies542 (7.83%)4.05%
Observational0 (0.00%)0.25%
Observational30 (0.43%)0.25%
Other10 (100.00%)84.16%
Other3,867 (55.87%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (366)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Single Dose, 4-Period, 2-Treatment Replicate Design Bioequivalency Study of Losartan Potassium/Hydrochlorothiazide Tablets 100 mg/25 mg Under Fasting Conditions [NCT01102478]30 participants (Actual)Interventional2005-02-28Completed
Prospective, Multicentric, Large Scale Observational Study to Evaluate the Effectiveness & Safety of Xirtam H in Indian Patients Suffering From Hypertension. [NCT01219556]8,704 participants (Actual)Observational2010-11-30Completed
Evaluation of an Optimization Protocol for Diuretics in the Decompensation of Chronic Heart Failure: Randomized Trial in Clusters With Sequential Permutation [NCT03892148]Phase 4300 participants (Anticipated)Interventional2019-05-17Recruiting
BP-EASE-A 12-Week, Multicenter, Open-Label, Randomized, Controlled Trial To Compare The Effectiveness of Losartan 50 mg/HCTZ 12.5 mg Titrated as Needed to Losartan 100 mg/HCTZ 25 mg or Valsartan 160 mg/HCTZ 25 mg, in Patients With Essential Hypertension W [NCT00546754]Phase 3808 participants (Actual)Interventional2007-05-01Completed
A Randomized, Double-Blind, Parallel-Filter Study to Evaluate the Antihypertensive Efficacy and Safety of Losartan-HCTZ Combination as Compared to Losartan Monotherapy in Patients With Essential Hypertension [NCT00307060]Phase 3274 participants (Actual)Interventional2004-12-01Completed
A Randomized, Open-label, Comparative, Non-inferiority, Multicenter Study to Compare Efficacy of Losartan Potassium Group and Carvedilol Group on Arterial Stiffness in Essential Hypertension Patients [NCT00496834]Phase 4201 participants (Actual)Interventional2008-02-01Completed
Comparison of the Impact of Nutritional Treatment vs Hydrochlorothiazide on Bone Mineral Density and Body Composition in Children With Idiopathic Hypercalciuria of the Hospital Infantil de Méxio Federico Gómez [NCT03951558]90 participants (Anticipated)Interventional2018-05-11Recruiting
Series of Single Patient Trials Comparing the Efficacy Between the Most Commonly Prescribed Thiazide Diuretic in the US, Hydrochlorothiazide, and Lisinopril for the Treatment of Stage 1 Hypertension. [NCT01258764]2 participants (Actual)Interventional2010-11-30Completed
Efficacy of Sevikar® Compared to the Combination of Perindopril/ Amlodipine on Central Arterial Blood Pressure in Patients With Moderate to Severe Hypertension- [NCT01101009]Phase 4486 participants (Actual)Interventional2010-04-30Completed
An Open Label, Randomized, 2-Period, 2-Treatment, Crossover, Single-Dose Bioequivalence Study of Fixed Dose Combination (FDC) of Losartan Potassium and Hydrochlorothiazide (100 mg / 25 mg Tablet) [Test Formulation, Torrent Pharmaceuticals Ltd., India] Ver [NCT01218711]Phase 10 participants InterventionalCompleted
Evaluation of the Antihypertensive Effect of Hyzaar(R) and Cognitive Function of Hypertensive Patients [NCT00398541]Phase 341 participants (Actual)Interventional2005-03-01Completed
A Randomised Double-blind Cross-over Single-centre Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension [NCT03276598]Phase 4233 participants (Actual)Interventional1999-11-25Completed
An Open-label, Randomized, Single-dose, Two-period Cross-over Study to Evaluate Bioequivalence of GSK3542503 Hydrochlorothiazide + Amiloride Hydrochloride 50 mg: 5 mg Fixed Dose Combination Tablets Versus Reference Product in Healthy Adult Participants Un [NCT03031496]Phase 142 participants (Actual)Interventional2017-03-17Completed
Acetazolamide and Hydrochlorothiazide Followed by Furosemide Versus Hydrochlorothiazide and Furosemide Followed by Furosemide for the Treatment of Adults With Refractory Nephrotic Edema: A Randomized, Double-Blind Trial [NCT02427880]Phase 420 participants (Actual)Interventional2015-04-30Completed
Bariatric Surgery and Pharmacokinetics Hydrochlorothiazide: BAR-MEDS Hydrochlorothiazide [NCT03476551]12 participants (Anticipated)Observational2016-11-02Recruiting
Safety and Efficacy of Hydrochlorothiazide in the Treatment of Hypernatremia in Critically Ill Patients: a Randomized Controlled Trial [NCT03658850]Phase 2184 participants (Anticipated)Interventional2018-10-01Recruiting
A Randomized Clinical Trial of the N-of-1 Approach in Children With Hypertension [NCT03461003]Phase 449 participants (Actual)Interventional2018-04-02Completed
HYZAAR Versus Ramipril Diabetic Patients [NCT00480805]Phase 3312 participants (Actual)Interventional2001-08-08Completed
Effect of Fixed Triple Combination With Losartan-Amlodipin-HCTZ vs. Free Triple Combination on Blood Pressure Control [NCT03578042]Phase 4100 participants (Anticipated)Interventional2017-04-01Recruiting
A Randomized, Placebo-Controlled, Double-Blind, Parallel Study of the Anti-Hypertensive Efficacy and Safety of Losartan Monotherapy as Compared to HCTZ Monotherapy and to the Combination of Losartan and HCTZ in Japanese Patients With Essential Hypertensio [NCT00092209]Phase 3840 participants Interventional2002-04-30Completed
A Randomized, Double-Blind, Multicenter, Phase 2/3 Study to Evaluate the Efficacy and Safety of Combined Administration of TAK-536CCB (Fix-dose Combination of Azilsartan and Amlodipine) and Hydrochlorothiazide in Comparison With TAK-536CCB or Hydrochlorot [NCT02072330]Phase 2/Phase 3353 participants (Actual)Interventional2013-03-31Completed
A Prospective, Open Label, Single Arm Study to Evaluate the Safety and Efficacy of an Olmesartan Medoxomil Based Treatment Regimen in Type II Diabetic Patients With Hypertension [NCT00403481]Phase 4192 participants (Actual)Interventional2006-11-30Completed
Pharmacokinetic Study of Propranolol, Losartan, and Eprosartan in Healthy Volunteers and Patients With Chronic Kidney Disease [NCT01087749]Phase 124 participants (Actual)Interventional2010-03-31Completed
An Open-Label, Six Month Safety Evaluation of the Fixed Dose Combination of Telmisartan 80 mg Plus Hydrochlorothiazide 12.5 mg in Patients With Mild-to-Moderate Hypertension [NCT02177487]Phase 3100 participants (Actual)Interventional1999-06-30Completed
The Effect and Safety of Amiloride in Decreasing Proteinuria for Patients With Chronic Kidney Disease in a Prospective , Crossover, Open-label Study. [NCT03170336]Phase 440 participants (Actual)Interventional2018-03-01Completed
Efficacy and Safety Evaluation of the New Association on Fixed Dose of Candesartan + Chlorthalidone, Produced by EMS S.A,in Arterial Hypertension Control [NCT02521233]Phase 30 participants (Actual)Interventional2016-11-30Withdrawn(stopped due to Sponsor decision)
Open-label, Randomised, 2-Arm Parallel Group, Multicentre, 8-week, Phase IV Study to Assess the Antihypertensive Efficacy and Safety of the Candesartan Cilexetil 16 mg and Hydrochlorothiazide 12.5 mg Combination Therapy in Comparison With Candesartan 16 m [NCT00621153]Phase 4214 participants (Actual)Interventional2008-02-29Completed
Matão Controlling Hypertension (MatCH Study): Rationale and Design. Project to Reduce Incidence of Arterial Hypertension in City of Matão, Brazil. [NCT03147092]Early Phase 115,000 participants (Anticipated)Interventional2018-02-01Not yet recruiting
An Open-label, Randomized, Single Dose, 6-Sequence, 3-Period, Cross-over Study to Evaluate a Drug Interaction Between Fixed-dose Combination of Fimasartan/Amlodipine and Hydrochlorothiazide in Healthy Male Subjects [NCT03390465]Phase 136 participants (Actual)Interventional2017-12-15Completed
An Open-Label, Superiority, Randomized, Comparative Study to Evaluate the Efficacy and Safety of Telmisartan, Amlodipine, and Chlorthalidone Fixed-Dose Combination Versus Telmisartan, Amlodipine, and Hydrochlorothiazide in Elderly Patients With Essential [NCT06041529]Phase 4250 participants (Anticipated)Interventional2023-09-14Not yet recruiting
Pharmacokinetics and Safety of Commonly Used Drugs in Lactating Women and Breastfed Infants [NCT03511118]1,600 participants (Anticipated)Observational2018-10-04Recruiting
A 2-Week, Randomized, Double-Blind, Parallel, Placebo-Controlled Study to Evaluate the Efficacy, Tolerability, and Pharmacokinetic-Pharmacodynamic Relationship of Fimasartan in Combination With Hydrochlorothiazide in Patients With Mild to Moderate Hyperte [NCT02222480]Phase 2103 participants (Actual)Interventional2014-10-31Completed
Relative Bioavailability of Telmisartan and HCTZ p.o. (80 mg Telmisartan/12.5 mg HCTZ) in Two Experimental Formulations (Given t.i.d. for One Day Each) Compared to the Standard Formulation 80 mg Telmisartan/12.5 mg HCTZ (MicardisPlus®), Given t.i.d. for O [NCT02262572]Phase 124 participants (Actual)Interventional2003-04-30Completed
Efficacy and Safety of Hydrochlorothiazide (HCTZ) Used as Add-on Therapy in Moderately to Severely Hypertensive Patients Not Adequately Controlled by Olmesartan Medoxomil (OM) 40 mg Monotherapy [NCT00430508]Phase 3972 participants (Actual)Interventional2007-02-28Completed
Evaluation of Platelet Effects of Chlorthalidone and Hydrochlorothiazide [NCT02100462]Phase 430 participants (Anticipated)Interventional2014-03-31Recruiting
A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Influence of Hydrochlorothiazide on Dermal Photosensitivity and DNA Stability - a Pilot Study (HCTox Study) [NCT04654312]Phase 130 participants (Actual)Interventional2021-01-18Completed
Comparison of the Efficacy of Olmesartan Medoxomil Versus Nitrendipine on Systolic Blood Pressure in Elderly and Very Elderly Patients With Isolated Systolic Hypertension [NCT00751829]Phase 3417 participants (Actual)Interventional2003-07-31Completed
A Double-blind, Randomized, Parallel 2- Arm Study to Compare the Efficacy of Ertugliflozin Versus Hydrochlorothiazide in Reducing Sympathetic Neural Overactivity in Patients With Hypertension and Recently-diagnosed Type 2 Diabetes Who Are Receiving Backgr [NCT03640221]Phase 40 participants (Actual)Interventional2018-09-01Withdrawn(stopped due to Study withdrawn prior to IRB approval and enrollment)
Prospective Multicenter Randomized Parallel Controlled Clinical Trial to Evaluate the Safety and Effectiveness of a Radiofrequency Renal Denervation System for the Treatment of Essential Hypertension [NCT03261375]205 participants (Actual)Interventional2021-01-19Completed
Relative Oral Bioavailability of 80 mg Telmisartan / 12.5 mg HCTZ Fixed Dose Combination Compared With Its Monocomponents in Healthy Subjects. A 4 Period Cross-over, Open, Randomized, Replicate Design Study. [NCT02176512]Phase 120 participants (Actual)Interventional1998-09-30Completed
A Phase Ib, Randomized, Double-Blind, 4-Treatment, 2-Period Incomplete Block Study to Evaluate the Multiple Dose Effects of MK-7145 and Hydrochlorothiazide Compared to Placebo on Blood Pressure in Male Patients With Hypertension [NCT01370655]Phase 146 participants (Actual)Interventional2011-06-15Completed
Bioequivalence of 80 mg Telmisartan/12.5 mg HCTZ of Fixed Dose Combination Compared to Its Monocomponents in Healthy Male Volunteers (an Open-label, Randomised, Single-dose, Two-way Crossover Study) [NCT02262624]Phase 136 participants (Actual)Interventional2005-02-28Completed
Bioequivalence of 80 mg Telmisartan/12.5 mg HCTZ Fixed Dose Combination Compared With Its Monocomponents in Healthy Male Volunteers II (an Open-label, Randomised, Single-dose, Two-sequence, Four-period Replicated Crossover Study) [NCT02262858]Phase 168 participants (Actual)Interventional2005-08-31Completed
Efficacy and Safety of Olmesartan Medoxomil/Hydrochlorothiazide Combination 20/25 mg Versus 40/25 mg in Moderately to Severely Hypertensive Patients Not Adequately Controlled by Olmesartan Medoxomil 40 mg Monotherapy [NCT00430950]Phase 31,011 participants (Actual)Interventional2007-02-28Completed
A Prospective, Open Label, Single Arm Study to Evaluation the Safety and Efficacy of an Olmesartan Medoxomil Based Treatment Regimen in Elderly Patients With Hypertension [NCT00412932]Phase 4178 participants (Actual)Interventional2006-12-31Completed
The Efficacy and Safety of Irbesartan/HCTZ Combination Therapy as First Line Treatment for Patients With Moderate Hypertension [NCT00095550]Phase 3496 participants (Anticipated)Interventional2004-10-31Completed
Efficacy of Telmisartan 40mg and Hydrochlorothiazide 25mg Monotherapy in High Sodium Intake Patients With Mild to Moderate Hypertension: a Multicenter Randomized Double-blinded Parallel Controlled Trial [NCT02255253]1,410 participants (Actual)Interventional2014-10-31Completed
An Open Label, Randomized, 2-Period, 2-Treatment, Crossover, Single-Dose Bioequivalence Study of Fixed Dose Combination (FDC) of Losartan Potassium and Hydrochlorothiazide (100 mg / 25 mg Tablet) [Test Formulation, Torrent Pharmaceuticals Ltd., India] Ver [NCT01218724]Phase 10 participants InterventionalCompleted
Reversal of an Unfavorable Effect of Hydrochlorothiazide Compared to Angiotensin Converting Enzyme Inhibitor on Serum Uric Acid and Oxypurines Levels by Estrogen-progestin Therapy in Hypertensive Postmenopausal Women. [NCT03921736]Phase 4180 participants (Actual)Interventional2000-01-10Completed
A PROBE (Prospective, Randomised, Open-label, Blinded Endpoint) Trial to Investigate the Efficacy and Safety of Telmisartan 40-80 mg Once Daily Compared With Losartan 50-100 mg Once Daily Over a Period of 12 Weeks, and of Telmisartan 80 mg + HCTZ 12.5 mg [NCT02172586]Phase 4363 participants (Actual)Interventional2000-01-31Completed
Open-Label Follow-up Trial on Efficacy and Safety of Chronic Administration of Telmisartan 80 mg (Micardis®) Tablets as Monotherapy or in Combination With Hydrochlorothiazide or Other Antihypertensive Medications in Patients With Mild to Moderate Hyperten [NCT02177422]Phase 3489 participants (Actual)Interventional1998-06-30Completed
An Eight Week Randomized, Double-Blind Study Comparing a Fixed Dose Combination of Telmisartan 40 mg Plus Hydrochlorothiazide 12.5 mg to Telmisartan 40 mg in Patients Who Fail to Respond Adequately to Treatment With Telmisartan 40 mg [NCT02177500]Phase 3327 participants (Actual)Interventional2000-01-31Completed
Bioequivalence of 40 mg Telmisartan / 12.5 mg HCTZ of Fixed Dose Combination Compared to Its Monocomponents in Healthy Male Volunteers (an Open-label, Randomised, Single-dose, Two-way Crossover Study) [NCT02262598]Phase 130 participants (Actual)Interventional2004-09-30Completed
A Double-blind, Randomized, Parallel-group, Placebo-controlled Pilot Study to Investigate the Magnitude and Duration of Response and the Safety of MK0954 (50 mg Given Once or Twice Daily, or 100 mg Given Once Daily) Compared to Placebo Using Ambulatory Bl [NCT00886600]Phase 3122 participants (Actual)Interventional1991-05-31Completed
A Relative Bioavailability Study of Moexipril HCL/Hydrochlorothiazide 15/25 mg Tablets Under Fasting Conditions [NCT00835042]Phase 160 participants (Actual)Interventional2003-10-31Completed
A Single Dose, 4-Period, 2-Treatment Replicate Design Bioequivalency Study of Losartan Potassium/Hydrochlorothiazide Tablets 100 mg/25 mg Under Fed Conditions [NCT01102465]25 participants (Actual)Interventional2005-02-28Completed
A 16-week Double-blind, Randomized, Multicenter, Force-titration Study to Evaluate the Antihypertensive Efficacy of Valsartan/Hydrochlorothiazide (HCTZ) Therapy Compared to HCTZ Based Therapy in Obese, Hypertensive Patients [NCT00439738]Phase 4412 participants (Actual)Interventional2006-12-31Completed
Irbesartan in the Treatment of Hypertensive Patients With Metabolic Syndrome [NCT00110422]Phase 4400 participants Interventional2005-11-30Completed
A Randomized, Placebo-controlled, Double Blind, 4-period, Cross-over Trial, to Study the Effects of Aliskiren, Hydrochlorothiazide and Moxonidine on Endothelial Dysfunction in Obesity Related Hypertension [NCT01138423]Phase 432 participants (Actual)Interventional2010-08-31Completed
Efficacy and Safety of Two Fixed-combination Antihypertensive Regimens, Amtrel® and Co-Diovan® in Type 2 Diabetes Hypertension Patients With Microalbuminuria [NCT01375322]Phase 4226 participants (Actual)Interventional2007-06-30Completed
A Comparison of Indapamide SR 1.5 mg With Hydrochlorothiazide 25 mg, in Combination With an ACE-inhibitor, in Old Patients With Mild to Moderate Renal Insufficiency and Hypertension [NCT01172431]Phase 4240 participants (Actual)Interventional2010-09-30Completed
A Randomized, Open Label, Multiple Dose, Crossover Study to Investigate Pharmacokinetic Drug Interactions Between Single and Concomitant Administrations of Amlodipine, Losartan, and Hydrochlorothiazide(HCTZ) in Subjects With (Pre)Hypertension [NCT01198249]Phase 123 participants (Actual)Interventional2010-09-30Completed
Efficacy of Chlorthalidone and Hydrochlorothiazide in Combination With Amiloride in Multiple Doses on Blood Pressure in Patients With Primary Hypertension: a Factorial Randomized Controlled Trial. [NCT03928145]Phase 384 participants (Anticipated)Interventional2019-11-13Recruiting
Efficacy and Safety Evaluation of the New Association on Fixed Dose of Candesartan Cilexetil + Chlorthalidone (16mg + 12.5mg and 16mg + 25mg) Compared With HYZAAR® in Hypertension Control [NCT02521246]Phase 30 participants (Actual)Interventional2016-11-30Withdrawn(stopped due to Sponsor decision)
A Randomized, Open-label, Single Dose, 3-way Crossover Study to Evaluate the Drug-drugs Interaction Between Telmisartan, Amlodipine and Hydrochlorothiazide in Healthy Male Volunteers [NCT03889145]Phase 130 participants (Actual)Interventional2013-12-19Completed
A TElmisartan and AMlodipine STudy to Assess the Cardiovascular PROTECTive Effects as Measured by Endothelial Dysfunction in Hypertensive at Risk Patients Beyond Blood Pressure [NCT01180205]Phase 4576 participants (Anticipated)Interventional2010-08-31Active, not recruiting
Randomized Open-label Trial to Evaluate the Effectiveness of Diet Management With a Losartan Titration Regimen Versus Losartan Titration Regimen Alone on Blood Pressure Reduction in Hypertensives. [NCT00739674]Phase 3992 participants (Actual)Interventional2008-02-01Completed
Evaluate the Safety and Tolerability of Hyzaar(R) (Losartan 50 Mg/ Hydrochlorothiazide 12.5 Mg) In the Treatment of Hypertension [NCT00400218]Phase 362 participants (Actual)Interventional2005-09-01Completed
A 24-week Trial of the Effectiveness and Safety of Fimasartan 60 mg Alone as Initial Treatment and Its Randomized Escalation to Fimasartan 120 mg or Fimasartan 60 mg/HCTZ 12.5 mg in Mexican Patients With Grade 1 and 2 Essential Hypertension [NCT02466490]Phase 3272 participants (Actual)Interventional2013-04-30Completed
A Prospective, Randomized, Open-label Clinical Trial to Evaluate the Effect of Tekturna (Aliskiren), Angiotensin Inhibitors, Diuretics, and Calcium Channel Blockers on Coronary Flow Reserve in Patients With Type II Diabetes and Hypertension [NCT00994253]Phase 40 participants (Actual)Interventional2009-08-31Withdrawn(stopped due to Due to safety concerns re: the concomitant use of aliskiren with an ACEi or ARB.)
A Phase 3, Open-Label, Randomized, Long-Term Comparison of the Safety and Tolerability of the TAK-491 Plus Chlorthalidone Fixed-Dose Combination vs. Olmesartan Medoxomil-Hydrochlorothiazide Fixed-Dose Combination in Subjects With Essential Hypertension [NCT00996281]Phase 3837 participants (Actual)Interventional2009-10-31Completed
The Efficacy and Safety of Losartan/Hydrochlorothiazide Combination Drug (Preminent) in Patients With Morning Hypertension [NCT00795847]Phase 4216 participants (Actual)Interventional2008-11-30Completed
Night-time Use of Thiazide Diuretics for Improved Reduction in Stone Risk in Stone Formers With Elevated Urine Calcium [NCT02711670]10 participants (Actual)Interventional2014-02-28Completed
A Prospective, Open-label, Ambulatory Blood Pressure Monitoring (ABPM) Dose Titration Study to Evaluate the Safety and Efficacy of an Olmesartan Medoxomil and Amlodipine Based Treatment Regimen in Hypertensive, Type 2 Diabetic Subjects [NCT00654745]Phase 4207 participants (Actual)Interventional2008-05-31Completed
A Relative Bioavailability Study of Moexipril HCl/Hydrochlorothiazide 15/25 mg Tablets Under Non-Fasting Conditions [NCT00834067]Phase 160 participants (Actual)Interventional2003-10-31Completed
An Eight Week Randomized, Double-Blind Study Comparing a Fixed Dose Combination of Telmisartan 80 mg Plus Hydrochlorothiazide 12.5 mg to Telmisartan 80 mg in Patients Who Fail to Respond Adequately to Treatment With Telmisartan 80 mg. [NCT02177435]Phase 3491 participants (Actual)Interventional1999-02-28Completed
Pharmacogenomics Of Hypertension: A New Approach For A Personalized Medicine [NCT03249285]Phase 3300 participants (Anticipated)Interventional2016-03-31Recruiting
A Randomized, Double-blind, Active-controlled, 2-parallel Group, Optional Titration, Multicenter, Phase 3b Study to Evaluate the Efficacy and Safety of Fimasartan Versus Perindopril Monotherapy With and Without Diuretics Combination in Elderly Patients Wi [NCT03246555]Phase 3241 participants (Actual)Interventional2016-07-15Completed
A Blinded Crossover Study of the 24 Hour Blood Pressure Response to Treatment of Obstructive Sleep Apnea Associated Hypertension With Nebivolol or Hydrochlorothiazide [NCT02710071]Phase 441 participants (Actual)Interventional2015-01-31Completed
A Randomised, Double- Blind, Placebo-controlled, 6 Week Parallel-group Trial on the Efficacy and Safety of the Angiotensin II Receptor Antagonist Micardis® (Telmisartan 20 mg, 40 mg or 80 mg, p.o. Once Daily) or Hydrochlorothiazide 12.5 mg p.o. Once Daily [NCT02175355]Phase 31,039 participants (Actual)Interventional1999-10-31Completed
A Multicenter, Double-blind, Controlled, Randomized Trial to Evaluate the Association Candesartan Cilexetil + Chlorthalidone + Amlodipine Versus Exforge HCT®️ for Systemic Arterial Hypertension [NCT05920005]Phase 3698 participants (Anticipated)Interventional2023-08-22Recruiting
A Prospective Randomised Open-Label Blinded Endpoint Trial Comparing Telmisartan 80 mg and Losartan 50 mg + Hydrochlorothiazide 12.5 mg (Fixed Dose Combination) in Patients With Mild-to-Moderate Essential Hypertension Using Ambulatory Blood Pressure Monit [NCT02183701]Phase 3715 participants (Actual)Interventional1998-04-30Completed
Relative Oral Bioavailability of 40 mg Telmisartan / 12.5 mg HCTZ Fixed Dose Combination Compared With Its Monocomponents in Healthy Subjects. A 4 Period Cross-over, Open, Randomized, Replicate Design Study [NCT02187523]Phase 132 participants (Actual)Interventional1999-10-31Completed
Open-label With Blinding Bioanalytical Stage Randomized Crossover Two Period Two Sequences Single Dose Bioequivalence Study of Two Formulations Ramipril/Hydrochlorothiazide Tablets 10 mg/25 mg (Manufacturer: Pharmtechnology LLC, Republic of Belarus) and T [NCT05685277]Phase 150 participants (Actual)Interventional2022-12-28Completed
An Open,Multicenter Study to Evaluate the Efficacy and Safety of a 4 Week Therapy With Valsartan/Hydrochlorothiazide 160/25 (Fixed Dose Combination of Valsartan 160 mg Plus HCTZ 25 mg) in Patients Not Adequately Responding to a 4 Week Monotherapy With Olm [NCT00171015]Phase 3212 participants (Actual)Interventional2004-12-31Completed
Clinical Study to Evaluate the Efficacy and Safety of the Combination Therapy Candesartan Cilexetil 32 mg Plus Hydrochlorothiazide 25 mg in Patients With Severe Hypertension [NCT01012479]Phase 4107 participants (Actual)Interventional2009-10-31Completed
Comparison of the Efficacy of Olmesartan Medoxomil Versus Losartan on Diastolic Blood Pressure in Elderly and Very Elderly Patients With Essential Hypertension. [NCT00751751]Phase 3441 participants (Actual)Interventional2003-06-30Completed
Vascular Improvement With Olmesartan Medoxomil Study [NCT00772499]Phase 4100 participants (Actual)Interventional2002-11-30Completed
A Randomized, Double-Blind, Active Comparator Study to Evaluate the Antihypertensive Efficacy and Safety of Losartan/HCTZ Combination as Compared to Losartan Monotherapy in Pediatric Patients With Essential Hypertension [NCT00447603]Phase 340 participants (Actual)Interventional2007-05-24Terminated(stopped due to Achieving site readiness and enrolling the trial within a reasonable time)
Association Between Angiotensin Converting Enzyme Inhibitor or Angiotensin Receptor Blocker Use and COVID-19 Severity and Mortality Among US Veterans [NCT04467931]22,213 participants (Actual)Observational2020-01-19Completed
Comparison of Effects Between Calcium Channel Blocker and Diuretics in Combination With Angiotensin II Receptor Blocker on 24-hr Central Blood Pressure and Vascular Hemodynamic Parameters in Hypertensive Patients Multicenter, Double-blind, Active-controll [NCT02294539]Phase 4231 participants (Actual)Interventional2014-08-31Completed
RESPECT: Observational, Prospective, Open-label, Multi-center Study Evaluating the Antihypertensive Effect of Treatment With Telmisartan (Alone or in Fixed Combination With HCTZ) in General Practitioner and Specialist Practice in Hypertensive Patients Wit [NCT00890084]2,913 participants (Actual)Observational2009-04-30Completed
Exploring the Association Between Phthalates Exposure, Measured Through Their Urinary Metabolites, and Renal Function Impairment in Individuals With TYpe 2 Diabetes - SGLT2 Subprotocol [NCT04242758]Phase 430 participants (Actual)Interventional2019-06-04Active, not recruiting
A Randomized, Open-label, Single Dose, Replicate Crossover Clinical Trial to Compare the Pharmacokinetics of TAH Tablet in Comparison to the Co-administration of Telmisartan, Amlodipine and Hydrochlorothiazide in Healthy Male Volunteers [NCT02739672]Phase 140 participants (Actual)Interventional2016-01-02Completed
Sympathetic Regulation of Large Artery Stiffness in Humans With Age-Related Isolated Systolic Hypertension [NCT04423627]Early Phase 178 participants (Anticipated)Interventional2021-06-01Recruiting
[NCT01858623]18 participants (Actual)Interventional2013-02-28Completed
Single-Dose Food In Vivo Bioequivalence Study of Metoprolol Tartrate/Hydrochlorothiazide Tablets (100/50 mg; Mylan) to Lopressor HCT® Tablets (100/50 mg; Novartis) in Healthy Volunteers [NCT00649233]Phase 132 participants (Actual)Interventional2003-01-31Completed
A Pilot Study of N-of-1 Trials of Blood Pressure Medications in Adults With Hypertension [NCT02744456]Early Phase 110 participants (Actual)Interventional2014-08-01Completed
A Phase III, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Factorial Study of Metoprolol Succinate Extended Release Tablets (TOPROL-XL) Hydrochlorothiazide and Their Combination in Patients With Essential Hypertension. [NCT00642096]Phase 31,900 participants (Anticipated)Interventional2003-06-30Completed
Single-Dose Food in Vivo Bioequivalence Study of Benazepril HCl and Hydrochlorothiazide Tablets (20 mg/25 mg; Mylan) to Lotensin HCT® Tablets (20 mg/25 mg; Novartis) in Healthy Volunteers [NCT00649038]Phase 124 participants (Actual)Interventional2002-12-31Completed
Dapagliflozin and Hydrochlorothiazide Treatment in Recurring Kidney Stone Patients - a Randomised Single Center Cross-over Study [NCT05443932]Phase 432 participants (Anticipated)Interventional2024-03-04Not yet recruiting
Effects of Intensive Antihypertensive Therapies on the Risk of Stroke in Hypertensive Adults: A Prospective Randomized Open-Label Blinded-Endpoint Trial, a Feasibility Study [NCT02817503]Phase 4100 participants (Anticipated)Interventional2015-12-31Enrolling by invitation
Use of Diuretics in Maintenance Hemodialysis Patients With Residual Renal Function Undergoing Bioimpedance-guided Fluid Management [NCT04182854]46 participants (Anticipated)Interventional2019-10-28Recruiting
Effects of Fluid Balance Control in Critically Ill Patients: A Multicenter Randomized Study [NCT02765009]1,411 participants (Actual)Interventional2016-06-01Completed
Single-Dose Fasting In Vivo Bioequivalence Study of Metoprolol Tartrate/Hydrochlorothiazide Tablets (100/50 mg; Mylan) and Lopressor HCT® Tablets (100/50 mg; Novartis) in Healthy Volunteers [NCT00649688]Phase 132 participants (Actual)Interventional2003-01-31Completed
An Evaluation of the Safety, Tolerability, and Pharmacodynamic Effects of GSK189075 When Administered With Furosemide or Hydrochlorothiazide [NCT00671424]Phase 148 participants (Anticipated)Interventional2008-03-31Completed
Irbesartan/Hydrochlorothiazide to Control Elevated Blood Pressure to Target in Moderate to Severe Hypertensive Patients [NCT00670566]Phase 4503 participants (Actual)Interventional2008-04-30Completed
A Study to Compare the Relative Bioavailability of Moexipril HCl/Hydrochlorothiazide 15mg/25mg Tablets (Paddock Laboratories, Inc) and Uniretic® 15mg/25mg Tablets (Schwarz Pharma)(Moexipril HCl/Hydrochlorothiazide) in Healthy Adult Volunteers Under Fastin [NCT00990301]Phase 148 participants (Actual)InterventionalCompleted
Comparison of Three Combination Therapies in Lowering Blood Pressure in Black Africans [NCT02742467]Phase 4702 participants (Actual)Interventional2017-06-07Completed
A Double-blind, Randomised, 4-arm Parallel Group, Multicentre, 8-week, Phase III Study to Assess the Antihypertensive Efficacy and Safety of the Combination of Candesartan Cilexetil (CC) 32 mg and Hydrochlorothiazide (HCT) 25 mg Compared With CC 32 mg, HC [NCT00434967]Phase 32,207 participants (Actual)Interventional2007-01-31Completed
A 25 Week, Open Label Study to Determine the Effects of Nebivolol When Added to Hydrochlorothiazide on Diastolic Function and Arterial Stiffness in African Americans With Hypertension [NCT00999752]40 participants (Actual)Interventional2009-10-31Completed
Evaluation of Drug-drug Interaction Between Henagliflozin Proline and Hydrochlorothiazide in Healthy Chinese Volunteers [NCT06083116]Phase 112 participants (Actual)Interventional2019-08-28Completed
A 54-week, Open-label, Multicenter Study to Assess the Long-term Safety and Tolerability of the Combination of Aliskiren 300 mg /Valsartan 320 mg in Patients With Essential Hypertension Followed by a 26 Week Open-label Extension to Assess the Long-term Sa [NCT00386607]Phase 3601 participants (Actual)Interventional2006-10-31Completed
A 36 Week Randomized, Double-blind, Parallel Group, Multi-center, Active-controlled, Optional Titration Study Comparing an Aliskiren-based Regimen to a Ramipril-based Regimen in Patients ≥ 65 Years Old With Systolic Essential Hypertension [NCT00368277]Phase 3901 participants (Actual)Interventional2006-09-30Completed
An 8-week Randomized, Double-blind, Parallel-group, Multi-center, Forced-titration Study to Evaluate the Efficacy and Safety of Aliskiren Plus HCTZ Compared to Aliskiren Monotherapy in Metabolic Syndrome Patients With Stage 2 Hypertension [NCT00797316]Phase 4532 participants (Actual)Interventional2008-11-30Completed
Postpartum Management of Hypertension in Pregnancy With Hydrochlorothiazide: a Randomized Clinical Trial [NCT03298802]Phase 3612 participants (Anticipated)Interventional2017-11-21Recruiting
A Phase 3, Double-Blind, Randomized, Efficacy and Safety Study of the TAK 491 Plus Chlorthalidone Fixed-Dose Combination Compared With TAK-491 and Hydrochlorothiazide Coadministration Therapy in Subjects With Moderate to Severe Essential Hypertension [NCT00818883]Phase 3609 participants (Actual)Interventional2009-02-28Completed
A Phase 3, Double-Blind, Randomized, Efficacy and Safety Study Comparing the TAK-491 Plus Chlorthalidone Fixed-Dose Combination vs Benicar HCT® (Olmesartan Medoxomil-Hydrochlorothiazide) in Subjects With Moderate to Severe Essential Hypertension [NCT00846365]Phase 31,085 participants (Actual)Interventional2009-03-31Completed
Alpha-blocker Plus Diuretic Combination Therapy as Second-line Treatment for Nocturia in Men With LUTS: a Pilot Study [NCT00700583]72 participants (Actual)Interventional2008-05-31Completed
Single-Dose Food In Vivo Bioequivalence Study of Quinapril HCl and Hydrochlorothiazide Tablets (20 mg/25 mg; Mylan) to Accuretic™ Tablets (20 mg/25 mg; Parke-Davis) in Healthy Volunteers [NCT00648011]Phase 144 participants (Actual)Interventional2003-08-31Completed
A 12-Week Open-Label, Uncontrolled Multicenter Study to Assess the Efficacy and Safety of Quinapril or Quinapril Plus Hydrochlorothiazide in Subjects With Mild to Moderate Hypertension [NCT00651287]Phase 4200 participants (Actual)Interventional2002-12-31Completed
An 8-week Randomized, Double-blind, Parallel-group, Multi-center, Active-controlled Dose Escalation Study to Evaluate the Efficacy and Safety of Aliskiren HCTZ (300/25 mg) Compared to HCTZ (25 mg) in Older Patients With Stage 2 Systolic Hypertension [NCT00760266]Phase 4451 participants (Actual)Interventional2008-09-30Completed
A Randomized Trial to Establish the Effects of Combination Pill of Losartan Potassium and Hydrochlorothiazide on Medication Compliance Among Patients With High Blood Pressure. [NCT00670787]Phase 3207 participants (Actual)Interventional2008-06-30Completed
An 8 Week Prospective, Multicenter, Randomized, Double-Blind, Active Control, Parallel Group Study to Evaluate the Efficacy and Safety of Aliskiren HCTZ Versus Amlodipine in African American Patients With Stage 2 Hypertension [NCT00739596]Phase 4332 participants (Actual)Interventional2008-07-31Completed
A Prospective, Open-Label, Titration Study to Evaluate the Efficacy and Safety Safety of AZOR in Multiple Subgroups of Hypertensive Subjects Who Are Non-Responders to Anti-Hypertensive Monotherapy [NCT00791258]Phase 4999 participants (Actual)Interventional2008-11-30Completed
A Comparison of Hydrochlorothiazide and Metolazone in Combination With Furosemide in Congestive Heart Failure Patients [NCT00690521]Phase 413 participants (Anticipated)Interventional2003-01-31Recruiting
Single Dose Two-Way Crossover Fasted Bioequivalence Study of Benazepril HCl/ Hydrochlorothiazide 20 mg/ 25 mg Tablets in Healthy Volunteers [NCT00778726]42 participants (Actual)Interventional2004-09-30Completed
Role of Mineralocorticoid Receptor in Diabetic Cardiovascular Disease [NCT00865124]69 participants (Actual)Interventional2008-09-30Completed
An 8 Week, Double-blind, Randomized, Parallel Group, Active-controlled Study to Evaluate the Efficacy and Safety of the Combination of Aliskiren/Amlodipine/Hydrochlorothiazide in Patients With Moderate to Severe Hypertension [NCT00765674]Phase 31,191 participants (Actual)Interventional2008-09-30Completed
A Randomized, Double-Blind, Placebo-Controlled, 2-Part Study to Evaluate the Multiple Dose Effects of Hydrochlorothiazide and Isosorbide Mononitrate on Glucose Homeostasis in Obese Patients With Hypertension [NCT00871871]Phase 164 participants (Actual)Interventional2009-03-31Completed
Efficacy and Safety of Irbesartan/Hydrochlorothiazide Combination: A Comparison of Active and Usual Titration Regimen in the Treatment of Hypertensive Patients Insufficiently Controlled by Monotherapy [NCT00708344]Phase 4832 participants (Actual)Interventional2008-06-30Completed
An 8-week Study to Evaluate the Efficacy and Safety of Aliskiren HCTZ (300/25 mg) Compared to Amlodipine (10 mg) in Patients With Stage 2 Systolic Hypertension and Diabetes Mellitus [NCT00787605]Phase 4860 participants (Actual)Interventional2008-11-30Completed
An Open-label, Randomized, Parallel Group Study Comparing the Efficacy and Safety of Amlodipine in Combination With Valsartan Compared to Losartan in Combination With Hydrochlorothiazide Given for 52 Weeks on the Regression of Left Ventricular Hypertrophy [NCT00446563]Phase 390 participants (Actual)Interventional2007-03-31Completed
A One-Year Phase 3, Open-Label Study to Evaluate the Safety and Tolerability of TAK-491 in Subjects With Essential Hypertension [NCT00695955]Phase 3669 participants (Actual)Interventional2007-06-30Completed
A Randomized, 32 Week Double-blind, Parallel-group, Multicenter Study to Compare the Efficacy and Safety of Initiating Treatment With Combination (Aliskiren/Amlodipine) Therapy in Comparison With the Sequential add-on Treatment Strategies in Patients With [NCT00797862]Phase 31,254 participants (Actual)Interventional2008-11-30Completed
An 8-week Multicenter, Randomized, Double-blind, Active Controlled, Parallel Group, Forced Titration Study to Evaluate the Efficacy and Safety of Aliskiren/Amlodipine/HCTZ Compared to Aliskiren/Amlodipine in US Minority Patients With Stage 2 Hypertension [NCT00942994]Phase 4412 participants (Actual)Interventional2009-06-30Completed
Comparison of the Medication Adherence of Patients Treated With Telmisartan/Hydrochlorothiazide or Telmisartan/Amlodipine Fixed Dose Combination (FDC) Versus Double-pill Combination Therapy Based on Database Data in Real-world Japanese Therapeutic Practic [NCT03205137]0 participants (Actual)Observational2022-06-01Withdrawn(stopped due to Sponsor decision)
A 28 to 54-week, Open-label, Multicenter Study to Assess the Long-term Safety and Tolerability of the Combination of Aliskiren / Amlodipine / Hydrochlorothiazide in Patients With Essential Hypertension [NCT00667719]Phase 3564 participants (Actual)Interventional2008-06-05Completed
A Bioequivalence Study of Test and Reference Fosinopril Sodium/ Hydrochlorothiazide 20/ 12.5 mg Tablets Under Non-Fasting Conditions [NCT00778713]33 participants (Actual)Interventional2003-03-31Completed
A Relative Bioavailability Study of 100/25 mg Losartan Potassium/Hydrochlorothiazide Tablets Under Fasting Conditions [NCT01149486]Phase 120 participants (Actual)Interventional2004-01-31Completed
An 8-Week Prospective, Multicenter, Randomized, Double-Blind, Active Control, Parallel Group Study to Evaluate the Efficacy and Safety of Aliskiren HCTZ vs Ramipril in Obese Patients (BMI ≥ 30) With Stage 2 Hypertension [NCT00772577]Phase 4386 participants (Actual)Interventional2008-08-31Completed
Single-Dose Fasting In Vivo Bioequivalence Study of Benazepril HCl and Hydrochlorothiazide Tablets (20 mg/25 mg; Mylan) to Lotensin HCT® Tablets (20 mg/25 mg; Novartis) in Healthy Volunteers [NCT00649597]Phase 156 participants (Actual)Interventional2002-11-30Completed
Comparison of Efficacy and Safety Between Benidipine and Hydrochlorothiazide in Fosinopril Treated Chronic Kidney Disease Patients With Hypertension: a Randomized Controlled Trial [NCT02646397]Phase 4508 participants (Anticipated)Interventional2016-02-29Not yet recruiting
A Randomized, Double-Blind, Parallel Group Study Evaluating the Efficacy and Safety of Co-Administration of a Triple Combination Therapy of Olmesartan Medoxomil, Amlodipine Besylate and Hydrochlorothiazide in Subjects With Hypertension [NCT00649389]Phase 32,500 participants (Actual)Interventional2008-05-31Completed
A 16 Week Multi-center, Randomized, Double-blind Study to Evaluate Efficacy and Safety of Valsartan/Hydrochlorothiazide (HCTZ) Combination Therapy Compared to Patients Initiated With Valsartan Monotherapy or Hydrochlorothiazide (HCTZ) Monotherapy in Very [NCT00698646]Phase 4384 participants (Actual)Interventional2008-04-30Completed
A Relative Bioavailability Study of Losartan Potassium/Hydrochlorothiazide 100/25 mg Tablets Under Non-Fasting Conditions [NCT01149473]Phase 180 participants (Actual)Interventional2004-03-31Completed
Randomized, Double-Blind, Multi-Center, Phase 3 Trial to Evaluate the Efficacy and Safety of Telmisartan/Amlodipine/Hydrochlorothiazide Combination in Comparison With Telmisartan/Amlodipine Combination for Essential Hypertension Patients Not Controlled by [NCT02738632]Phase 3300 participants (Anticipated)Interventional2015-05-31Completed
Newer vs Older Antihypertensive Agents in African Hypertensive Patients Trial [NCT01030458]Phase 4183 participants (Actual)Interventional2010-09-30Completed
A 4-Week, Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging, Parallel Group Study To Evaluate The Safety, Tolerability And Efficacy Of Once Daily PF-04971729 And Hydrochlorothiazide In Patients With Type 2 Diabetes Mellitus With Inadequa [NCT01096667]Phase 2194 participants (Actual)Interventional2010-05-17Completed
Randomised, Double-Blind, Parallel-Group Study Evaluating Efficacy and Safety of Co-Administration of Triple Combinations of Olmesartan Medoxomil, Amlodipine Besylate, and Hydrochlorothiazide Compared With Corresponding Olmesartan - Amlodipine Combination [NCT00923091]Phase 32,689 participants (Actual)Interventional2009-06-30Completed
Pharmacodynamic Evaluation of the ANTICALCIURIC Effect of Hydrochlorothiazide in Dent's Disease [NCT00638482]Phase 2/Phase 310 participants (Actual)Interventional2003-07-31Terminated(stopped due to terminated)
A Prospective Multicenter Randomized Controlled Trial of Efficacy and Safety of Renal Denervation for Resistant Hypertension [NCT02900729]Phase 3254 participants (Anticipated)Interventional2016-10-31Not yet recruiting
Mitigating the Pro-inflammatory Phenotype of Obesity [NCT04934228]Phase 160 participants (Anticipated)Interventional2021-07-01Recruiting
An Open Label, Balanced, Randomised, Two-Treatment, Four-Period, Two-Sequence, Single-Dose, Crossover, Fully Replicated Bioavailability Study on Fixed-Dose Combination of Quinapril 20 mg and Hydrochlorothiazide 25 mg Tablets of OHM Laboratories Inc.(Divis [NCT00872235]40 participants (Actual)Interventional2005-06-30Completed
An Open Label, Balanced, Randomized, Two-Treatment, Two-Period, Two-Sequence, Single-Dose, Crossover Bioavailability Study Comparing Fixed Dose Combination of Quinapril HCl 20 mg and Hydrochlorothiazide 25 mg Tablets of OHM Laboratories Inc (a Subsidiary [NCT00872781]64 participants (Actual)Interventional2007-10-31Completed
Evaluation of the Real-life Efficacy and Safety of a Fixed-dose Telmisartan/Hydrochlorothiazide, Including Its Effect on Plasma Potassium and on Glucose and Lipid Metabolism Parameters in Patients With Essential Arterial Hypertension [NCT01392534]1,586 participants (Actual)Observational2010-07-31Completed
A Study Assessing the Effect of Cardiovascular Medications Provided as Low-cost, Evidence-based Generic Samples [NCT00761904]660 participants (Anticipated)Interventional2010-12-31Not yet recruiting
52 Week Study to Evaluate the Effects of LOSARTAN 50 mg, 100 mg, 100/12.5 mg HCTZ, 100/25 mg HCTZ on Metabolic Parameters, Blood Pressure and Safety in Hypertensive Patients With Metabolic Syndrome [NCT00546052]Phase 31,738 participants (Actual)Interventional2005-09-01Completed
Multi-center Open Label, Non-comparative Observational Study of Irbesartan-Hydrochlorothiazide in the Treatment of Hypertension in Chinese Population [NCT00847834]Phase 4968 participants (Actual)Interventional2003-12-31Completed
Monotherapy Versus Dual Therapy for Initial Treatment for Hypertension [NCT00994617]Phase 4600 participants (Anticipated)Interventional2010-01-31Recruiting
Single-Dose Fed Bioequivalence Study of Olmesartan Medoxomil and Hydrochlorothiazide Tablets (40 mg/25 mg; Mylan) to Benicar HCT® Tablets (40 mg/25 mg; Sankyo) in Healthy Volunteers [NCT01019590]Phase 136 participants (Actual)Interventional2006-11-30Completed
Single-Dose Fasting Bioequivalence Study of Olmesartan Medoxomil and Hydrochlorothiazide Tablets (40 mg/25 mg; Mylan) to Benicar HCT® Tablets (40 mg/25 mg; Sankyo) in Healthy Volunteers [NCT01020214]Phase 136 participants (Actual)Interventional2006-11-30Completed
Data Collection on Hypertension and Its Treatment With Kinzal®/ Kinzalplus® [NCT00927537]2,052 participants (Actual)Observational2008-04-30Completed
A Post Marketing Observational Study to Investigate the Efficacy, Safety, Tolerability and the Effect on Quality of Life of Telmisartan (Micardis) and Telmisartan With HCTZ (Micardis Plus) in Patients With Hypertension [NCT00904215]1,095 participants (Actual)Observational2005-02-28Completed
Single Dose Crossover Comparative Bioavailability Study of Olmesartan Medoxomil/Hydrochlorothiazide 40 mg/25 mg Film-Coated Tablets in Healthy Adult Subjects / Fasting State [NCT04138888]Phase 132 participants (Anticipated)Interventional2019-10-31Recruiting
A 12-week Multicenter, Randomized, Double-blind, Parallel-group, Active-control Study to Evaluate the Antihypertensive Efficacy and Safety of Valsartan/Amlodipine-based Regimen Versus a Losartan-based Regimen in Patients With Stage 2 Systolic Hypertension [NCT00931710]Phase 4488 participants (Actual)Interventional2009-07-31Completed
An Open Label, Balanced, Randomized, Two-Treatment, Two-Period, Two- Sequence, Single-Dose, Crossover Bioavailability Study Comparing Hydrochlorothiazide 50 mg Tablet of Ohm Laboratories (A Subsidiary of Ranbaxy Pharmaceuticals USA) With Hydrochlorothiazi [NCT00776646]36 participants (Actual)Interventional2006-05-31Completed
A Bioequivalence Study of Test and Reference Fosinopril Sodium/ Hydrochlorothiazide 20/12.5 mg Tablets Under Fasting Conditions [NCT00777972]34 participants (Actual)Interventional2003-03-31Completed
DD-study: Diet or Diuretics for Salt-sensitivity in Chronic Kidney Disease [NCT02875886]Phase 428 participants (Actual)Interventional2016-09-30Completed
Single Dose Two-Way Crossover Fed Bioequivalence Study of Benazepril HCl/ Hydrochlorothiazide 20 mg/ 25 mg Tablets in Healthy Volunteers [NCT00778674]30 participants (Actual)Interventional2004-10-31Completed
Association of Diuretics With Change in Extracellular Volume, Natriuretic Peptides, Symptoms, and Cardiovascular Outcomes in CKD [NCT05171686]Phase 446 participants (Anticipated)Interventional2023-02-01Recruiting
Add-on Study of Hydrochlorothiazide in Patients With Moderate to Severe Hypertension Not Achieving Target Blood Pressure on Olmesartan/Amlodipine Alone [NCT00902538]Phase 32,204 participants (Actual)Interventional2009-04-30Completed
Double-blind, Randomized Trial to Investigate the Antihypertensive and Metabolic Effects of Candesartan in Insulin-resistant Obese Patients With a Hypertension Not Adequately Controlled by Previous ß-blocker or Calcium Channel Blocker [NCT00775814]Phase 4188 participants (Actual)Interventional2006-10-31Completed
A Phase 1, Single-Center, Open-Label, Two-Period, Single-Sequence, Multiple Dosing Drug-Drug Interaction Study of Sotagliflozin and Hydrochlorothiazide in Healthy Male and Female Subjects [NCT03387657]Phase 116 participants (Actual)Interventional2018-01-03Completed
An Open-label, Multicenter Study to Evaluate the Efficacy and Tolerability of a 4 Week Therapy With the Fixed Dose Combination of Amlodipine 10 mg Plus Valsartan 160 mg in Hypertensive Patients Not Adequately Responding to a 4 Week Therapy With the Free C [NCT00523744]Phase 3257 participants (Actual)Interventional2007-07-31Completed
Treat-to-Target Study of Olmesartan Medoxomil and an Add-on Treatment Algorithm Consisting of Hydrochlorothiazide and Amlodipine Besylate in Patients With Mild to Moderate Hypertension [NCT00311155]Phase 4694 participants (Actual)Interventional2006-03-31Completed
A Clinical Trial of Renin Profiling in Selection of Initial Antihypertensive Drug [NCT00834600]185 participants (Actual)Interventional2005-12-31Completed
[NCT00000525]Phase 3233 participants (Actual)Interventional1986-07-31Completed
A Comparison of Indapamide SR 1.5 mg With Hydrochlorothiazide 25 mg, in Combination With an ACE-inhibitor, in Patients With Mild to Moderate Hypertension and Type 2 Diabetes Mellitus [NCT00980187]Phase 456 participants (Actual)Interventional2008-03-31Completed
A Randomized, Double-blind, Double-dummy, Multicenter Clinical Trial to Evaluate the Additional Efficacy and Safety of Olmesartan Medoxomil 20mg / Hydrochlorothiazide 12.5mg in the Treatment of Chinese Patients With Mild to Moderate Essential Hypertension [NCT00872586]Phase 3304 participants (Actual)Interventional2006-08-31Completed
Prospective, Multicentric, Open Clinic Essay to Evaluate the Use of OLMETEC® (Olmesartan Medoxomile) and OLMETEC PLUS® (Olmesartan Medoxomile Hydrochlorothiazide) in Stade I and II, According to JNC VII [NCT00811226]450 participants (Anticipated)Observational2007-04-30Completed
A 16 Week Study to Evaluate the Effect on Insulin Sensitivity of Valsartan and Hydrochlorothiazide Combined and Alone, in Patients With Metabolic Syndrome [NCT00170937]Phase 4507 participants Interventional2004-11-30Completed
A 26-week Double-blind, Randomized, Multicenter Parallel-group Trial to Compare the Effects of Valsartan Versus Atenolol on Exercise Capacity in Hypertensive Overweight Postmenopausal Women With Impaired Exercise Tolerance [NCT00171132]Phase 464 participants (Actual)Interventional2004-08-31Completed
A 24-week Study to Evaluate the Effectiveness of Valsartan in Combination With Hydrochlorothiazide Versus Amlodipine on Arterial Compliance in Patients With Hypertension, Type 2 Diabetes and Albuminuria [NCT00171561]Phase 4144 participants (Actual)Interventional2003-03-31Completed
Effect of Active Telephone Calls in the Compliance of Hypertensive Patients With Treatment: An Open and Randomized Clinical Trial [NCT00813722]Phase 4400 participants (Actual)Interventional1999-03-31Active, not recruiting
The Vascular Effects of Carvedilol Controlle Release (CR) + Lisinopril Versus Lisinopril + Hydrochlorothiazide (HCTZ) in Abdominally Obese Hypertensive Patients [NCT00459056]Phase 325 participants (Actual)Interventional2007-04-30Completed
A Double-Blind, Randomized, Placebo Controlled, Parallel Group Study to Compare the Safety and Efficacy of an Olmesartan Medoxomil Based Treatment Regimen to Placebo in Patients With Stage I and Stage II Hypertension [NCT00430638]Phase 4278 participants (Actual)Interventional2006-12-31Completed
A Randomized, Open-label, Multicenter, Cross-over Trial to Evaluate the Efficacy of a 20 Week Treatment of Valsartan 320 mg Versus Atenolol 100 mg in Combination With Hydrochlorothiazide on Microcirculation in Hypertensive Patients [NCT00396656]Phase 330 participants (Actual)Interventional2005-12-31Completed
A Prospective, Multinational, Multicenter Trial to Compare the Effects of Amlodipine/Benazepril to Benazepril and Hydrochlorothiazide Combined on the Reduction of Cardiovascular Morbidity and Mortality in Patients With High Risk Hypertension [NCT00170950]Phase 311,506 participants (Actual)Interventional2003-10-31Terminated(stopped due to The study was terminated early because of significant efficacy results for the primary endpoint in favor of benazepril/amlodipine treatment.)
A Prospective Observational Study to Evaluate the Efficacy of Lodoz in a Population of Hypertensive Patients [NCT01080742]1,007 participants (Actual)Observational2010-01-31Completed
An Open Label, Single Arm Prospective Study to Evaluate Efficacy and Safety of Losartan Based Therapy Reslio® (Losartan) and Resilo-h® (Losartan+Hydrochlorthiazide) in Diabetic and Uncontrolled Hypertensive Patients [NCT03978884]Phase 40 participants (Actual)Interventional2019-06-01Withdrawn(stopped due to Unable to effective arrange trial logistics)
Multi-center, Open Label, 18-week Study to Demonstrate the Efficacy and Safety of Combination Therapy of Aliskiren/Amlodipine or Aliskiren/Amlodipine/Hydrochlorothiazide in Patients With Stage II HT [NCT01070030]Phase 4230 participants (Actual)Interventional2010-01-31Completed
A Randomized, Placebo-Controlled, Double-Blind, Phase IIa Study of Amiloride in the Treatment of Acute Autoimmune Optic Neuritis [NCT01879527]Phase 278 participants (Anticipated)Interventional2014-03-31Recruiting
Prospective, Randomized, Open-label, Blinded Endpoint, Forced Titration Study to Compare Telmisartan Combined With HCTZ (80mg/12.5mg), to Valsartan Combined With HCTZ (160mg/12.5mg), for the Control of Mild-to-moderate Hypertension in Obese Patients With [NCT00239538]Phase 4840 participants (Actual)Interventional2003-01-31Completed
A Comparison of Telmisartan 80 mg + Hydrochlorothiazide 12.5 mg With Amlodipine 10 mg + Hydrochlorothiazide 12.5 mg in the Control of Blood Pressure in Older Patients With Predominantly Systolic Hypertension. A Prospective, Randomised, Open-label, Blinded [NCT00240474]Phase 41,000 participants Interventional2002-12-31Completed
Randomized Open Clinical Trial to Compare the Effectiveness of the Administration of Diuretics in Hemodialysis Patients With Residual Renal Function in Single Centre [NCT01977430]Phase 436 participants (Anticipated)Interventional2013-11-30Recruiting
The Usefulness of Non-invasive Assessment of Haemodynamic Profile in the Diagnosis and Treatment of Hypertension [NCT01996085]144 participants (Actual)Interventional2013-01-31Completed
Management of Resistant Hypertension -Pharmacokinetic Assessment of Different Antihypertensive Regimen -Comparison of Two Treatment Strategies: Increase Sodium Depletion or Combined Blockage of Renin-angiotensin System (RAS) [NCT00224549]Phase 4180 participants (Actual)Interventional2005-04-30Completed
A Single-blind, Double Dummy, Randomized, Multi-dose, Two Sequence, Crossover, Study to Investigate the Effects of Renin Inhibitor (Aliskiren 300 mg) on Albuminuria in Non-diabetic Nephropathy Patients Treated With Ramipril 10 mg and Volume Intervention ( [NCT01302899]Phase 28 participants (Actual)Interventional2011-01-31Terminated(stopped due to In consequence of termination of ALTITUDE. A number of studies were continued in consultation with the Altitude Data Monitoring Committee.)
An Exploratory Phase 2 Study to Assess the Effect of Dapagliflozin on Glomerular Filtration Rate (GFR) in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic and Blood Pressure (BP) Control [NCT00976495]Phase 2154 participants (Actual)Interventional2009-10-31Completed
A Randomized, Double-blind, Parallel Group, Active-controlled, 38-week Study to Evaluate the Efficacy of Valsartan Versus Amlodipine on the Arterial Properties of Postmenopausal Women With Mild to Moderate Hypertension [NCT00171054]Phase 4125 participants (Actual)Interventional2003-09-30Completed
Treatment of HYpertension: Morning Versus Evening [NCT02214498]Phase 4120 participants (Anticipated)Interventional2015-05-31Not yet recruiting
A Randomized, Open-label, Positive Drug Controlled Clinical Trials to Compare the Efficacy of Nitrendipine and Hydrochlorothiazide , Captopril Plus Hydrochlorothiazide and Beijing Hypotensive No.0 in Tibetan Hypertension [NCT02217852]Phase 4800 participants (Anticipated)Interventional2014-08-31Not yet recruiting
A Randomised, Double-blind, Double Dummy, Active Controlled, Parallel Group, Forced Titration Study to Compare the Fixed-dose Combination of Telmisartan 80mg Plus Hydrochlorothiazide 25mg (T80/HCTZ25) Versus Telmisartan 80mg (T80) Monotherapy as First Lin [NCT00926289]Phase 4894 participants (Actual)Interventional2009-06-30Completed
Aldosterone and the Metabolic Syndrome: Renin Inhibition Versus Mineralocorticoid Receptor (MR) Antagonism [NCT01103245]Phase 169 participants (Actual)Interventional2010-03-31Completed
Regression of Fatty Heart by Valsartan Therapy [NCT00745953]Phase 40 participants (Actual)Interventional2007-08-31Withdrawn
A 54-week, Open-label, Multicenter Study to Assess the Long-term Safety and Tolerability of the Combination of Aliskiren 300 mg / Amlodipine 10 mg in Patients With Essential Hypertension [NCT00402103]Phase 3556 participants (Actual)Interventional2006-11-30Completed
ANALYSIS OF THE EFFECTIVENESS OF A STAGED MANAGEMENT PROGRAM AIMED AT CONTROLLING BLOOD PRESSURE AND BLOOD GLUCOSE OF TYPE 2 DIABETIC PATIENTS USING EXCLUSIVELY THE RESOURCES AVAILABLE IN A PRIMARY CARE SETTING IN BRAZIL [NCT00935805]124 participants (Anticipated)Observational2006-07-31Active, not recruiting
Project to Promote the Evaluation of the Cardiovascular Risk in the Clinical Practice and to Evaluate Its Evolution Following the Implementation of a Preventive Multifactorial Strategy Aimed to Reduce the Total Risk Level (SCORE Algorithm), in Subjects Su [NCT00821574]Phase 4144 participants (Actual)Interventional2005-07-31Completed
A Phase 3b, Double-Blind, Randomized, 12-Week Efficacy and Safety Study Comparing the TAK-491 Plus Chlorthalidone Fixed-Dose Combination vs Olmesartan Medoxomil-Hydrochlorothiazide in Subjects With Moderate to Severe Hypertension [NCT01033071]Phase 31,071 participants (Actual)Interventional2010-01-31Completed
Single-Dose Fasting In Vivo Bioequivalence Study of Quinapril HCl and Hydrochlorothiazide Tablets (20 mg/25 mg; Mylan) to Accuretic™ Tablets (20 mg/25 mg; Parke-Davis) in Healthy Volunteers [NCT00649441]Phase 160 participants (Actual)Interventional2003-08-31Completed
The Japan-Combined Treatment With Olmesartan and a Calcium Channel Blocker Versus Olmesartan and Diuretics Randomized Efficacy Study (J-CORE) [NCT00607035]Phase 4220 participants (Actual)Interventional2006-05-31Completed
"The ALiskiren or Losartan Effects on bioMARKers of Myocardial Remodeling (ALLMARK) Study" [NCT01176032]Phase 474 participants (Actual)Interventional2010-06-30Completed
Single-Dose Fasting In-Vivo Bioequivalence Study of Hydrochlorothiazide Tablets (50 mg; Mylan) to Hydrochlorothiazide Tablets (50 mg; Ivax) in Healthy Volunteers [NCT00649324]Early Phase 140 participants (Actual)Interventional2005-10-31Completed
An Open-label, Multiple-dosing, Crossover, and Parallel Study to Evaluate the Safety and Pharmacokinetics After Oral Concurrent Administration of Fimasartan and Hydrochlorothiazide in Healthy Male Volunteers [NCT00923533]Phase 134 participants (Actual)Interventional2009-03-31Completed
An Open-Label, Randomized, 2-Period Crossover Study to Evaluate the Bioequivalence After Administration of a Losartan 100-mg/Hydrochlorothiazide 12.5-mg Combination Tablet and the Coadministration of a Currently Marketed COZAAR™ 100-mg Tablet and MICROZID [NCT00953680]Phase 177 participants (Actual)Interventional2004-04-30Completed
A Multicenter, Open-Label, Single-Arm, Free Tablet Combination, Long-Term Study to Evaluate the Safety of Nebivolol in Combination With Valsartan in Patients With Stage 1 or Stage 2 Essential Hypertension [NCT01415505]Phase 3812 participants (Actual)Interventional2011-08-31Completed
A Randomized, Double-blind, Placebo-controlled, Forced-titration, Phase IV Study Comparing Telmisartan 80 mg + Hydrochlorothiazide 25 mg Versus Valsartan 160 mg + Hydrochlorothiazide 25 mg Taken Orally for Eight Weeks in Patients With Stage 1 or Stage 2 H [NCT00168779]Phase 41,185 participants Interventional2005-09-30Completed
Valsartan Plus Hydrochlorothiazide in Patients With Hypertension and Cardiovascular Risk Factors [NCT00171782]Phase 476 participants (Actual)Interventional2004-02-29Completed
An Open-label, Multicenter Study to Evaluate the Efficacy and Safety of a 4 Week Therapy With Aliskiren 300 mg Plus Hydrochlorothiazide 25 mg in Hypertensive Patients Not Adequately Responding to a 4 Week Therapy With Candesartan 32 mg Plus Hydrochlorothi [NCT00867490]Phase 3186 participants (Actual)Interventional2009-03-31Completed
A Phase IV Clinical Trial of Intensified Blood Pressure Management in Primary Care Using Valsartan Alone and as Combination Anti-Hypertensive Therapy [NCT00902304]Phase 42,337 participants (Actual)Interventional2009-07-31Completed
Pharmacogenetic of the Antihypertensive Response to the Angiotensin II Blockers in Monotherapy or Associated to Hydrochlorothiazide [NCT00617877]800 participants (Actual)Interventional2005-03-31Completed
ONgoing Evaluation of Depressor Effect And Safety of Combination Therapy With Telmisartan and Low-dose Hydrochlorothiazide in Patients With Hypertension Uncontrolled on Amlodipine Treatment [NCT00509470]Phase 475 participants (Actual)Interventional2007-07-31Completed
Add-on Study of Olmesartan Medoxomil in Patients With Moderate to Severe Hypertension Not Achieving Target Blood Pressure on Amlodipine 5 mg Alone [NCT00220233]Phase 3632 participants Interventional2005-04-30Completed
[NCT01858610]18 participants (Actual)Interventional2013-03-31Completed
Multi-Omics to Predict the Blood Pressure Response to Antihypertensives [NCT05917275]Phase 496 participants (Anticipated)Interventional2023-10-31Not yet recruiting
A Multi-center, Multiple Dose, Open-label, Four-cohort, Parallel Study to Assess the Pharmacokinetic Drug Interaction Following Co-administration of Valsartan, Hydrochlorothiazide and Amlodipine in Patients With Hypertension. [NCT00548067]Phase 3111 participants (Actual)Interventional2007-09-30Completed
Morning Hypertension and Monitoring of Metabolism (AWB Morgenhochdruck & Stoffwechselmonitoring) [NCT02242383]13,248 participants (Actual)Observational2005-01-31Completed
A 52-week Extension to the Factorial Study to Evaluate the Efficacy and Safety of VAH631 (Valsartan and Hydrochlorothiazide Combined) and Alone in Essential Hypertensive Patients - Long Term Study of VAH631 in Patients With Essential Hypertension (Extensi [NCT00338936]Phase 3362 participants (Actual)Interventional2006-05-31Completed
Metabolic Effects of Antihypertensive Drugs [NCT00887510]Phase 424 participants (Actual)Interventional2007-05-31Completed
Post Marketing Surveillance on Long Drug Use of Micombi Combination Tablets in Patients With Hypertension [NCT01050062]1,452 participants (Actual)Observational2010-01-31Completed
A Phase III, Randomized, Active-Comparator Controlled Clinical Trial to Study the Efficacy and Safety of MK-0954E in Japanese Patients With Essential Hypertension Uncontrolled With Losartan and Amlodipine Co-administration [NCT01302691]Phase 3327 participants (Actual)Interventional2011-01-01Completed
Comparative Trial of Combination Therapy of ARB/Diuretic Versus ARB/CCB in Uncontrolled Hypertensive Patients With Monotherapy of ARB [NCT00492128]Phase 4196 participants (Actual)Interventional2007-09-30Completed
Influence of Food on the Bioavailability of Telmisartan 40 mg/HCTZ 12.5 mg Fixed-dose Combination and of Telmisartan 80 mg/HCTZ 12.5 mg Fixed-dose Combination in Japanese Healthy Male Volunteers (an Open-label, Randomised, Single-dose, Two-way Crossover S [NCT02276378]Phase 132 participants (Actual)Interventional2008-07-31Completed
Anxiety-mediated Impairments in Large Elastic Artery Function and the Autonomic Nervous System [NCT03109795]Phase 430 participants (Actual)Interventional2017-04-10Terminated(stopped due to Funding ended)
Genetic Epidemiology of Responses to Antihypertensives [NCT00005520]1,200 participants (Actual)Observational1997-02-28Completed
A Double-Blind, Randomized, Parallel Design Study of Aliskiren Versus Hydrochlorothiazide in Mild-to Moderate Hypertensive Type II Diabetes Mellitus Patients on Remodeling of Resistance Arteries [NCT01480791]Phase 20 participants (Actual)Interventional2012-01-31Withdrawn(stopped due to Because of results of Altitude trial, this trial was cancelled.)
An Open Label, Randomized, 2-Period, 2-Treatment,2-Sequence, Crossover, Single-Dose BE of FDC of Olmesaartan Medoxomil, Amlopdipine and Hydrochlorothiazide (40+10+25) mg Tab [Torrent,India] Vs Tribenzor(40+10+25) mg Tab [ Daichi Sankyo, Inc USA] in Health [NCT02962336]Phase 134 participants (Actual)Interventional2011-05-31Completed
A Randomised, Double-blind, Double-dummy, Placebo-controlled, Forced-titration, Comparison of MICARDIS® HCT (Telmisartan 80 mg / Hydrochlorothiazide 25 mg) Versus DIOVAN® HCT (Valsartan 160 mg / Hydrochlorothiazide 25 mg) Using Seated Trough Cuff Blood Pr [NCT00240448]Phase 41,109 participants (Actual)Interventional2003-09-30Completed
Intensive Non-Sympathetic Activating Vasodilatory Treatment in Hypertensive Patients With Microvascular Angina Pectoris [NCT00424801]10 participants (Actual)Interventional2007-01-31Terminated(stopped due to Due to recent findings relating MRI contrast to nephrogenic systemic fibrosis)
An Open-label Follow-up Trial of the Efficacy and Safety of Chronic Administration of the Fixed Dose Combination of Telmisartan 80 mg + Hydrochlorothiazide 25 mg Tablets Alone or in Combination With Other Antihypertensive Medications in Patients With Hype [NCT00267943]Phase 3639 participants Interventional2006-01-31Completed
A 6-week Treatment Regimen Study to Evaluate the Efficacy of Initial High Dose Valsartan Monotherapy (160 mg) or Combo Therapy (Valsartan + Hydrochlorothiazide, 160/12.5 mg) to Conventional Low-dose Valsartan Monotherapy (80 mg) in Managing Patients With [NCT00280540]Phase 4648 participants Interventional2005-12-31Completed
A 36 Week Three-Center Double-Blind Randomized Cross-Over Trial Comparing Metabolic Effects of Candesartan, Hydrochlorothiazide and Placebo [NCT00282178]Phase 226 participants (Actual)Interventional2005-04-30Completed
A Multi-center, Factorial Study to Evaluate Efficacy & Safety of 8 Wks Treatment With VAH631 [Valsartan (40 & 80 mg) and Hydrochlorothiazide (6.25 & 12.5 mg) Combined & Alone in Essential Hypertensive Patients] - Double-blind Study of VAH631 in Patients W [NCT00311740]Phase 3582 participants (Actual)Interventional2006-03-31Completed
Effect of Renin-angiotensin-system Blockade on Urinary Free Light Chains in Patients With Type 2 Diabetes Mellitus [NCT02046395]Phase 428 participants (Actual)Interventional2012-01-31Completed
A Double-blind, Randomized, Multicenter Study to Evaluate the Effectiveness of the Combination of Valsartan & Amlodipine in Hypertensive Patients Not Controlled on Monotherapy [NCT00327145]Phase 3894 participants (Actual)Interventional2006-03-31Completed
The Comparison of the Antihypertensive Efficacy and Tolerability Between Valsartan Plus Hydrochlorothiazide 80mg/12.5mg and Amlodipine 5mg in the Essential Hypertensive Patients [NCT00426478]Phase 480 participants (Anticipated)Interventional2006-11-30Completed
A Randomized, Double-Blind, Parallel-Group Assessment of the Safety and Efficacy of Telmisartan 40mg Plus Hydrochlorothiazide 12.5 mg in Comparison With Losartan 50 mg Plus Hydrochlorothiazide 12.5 mg in Taiwanese Patients With Mild to Moderate Hypertensi [NCT00133185]Phase 331 participants Interventional2004-03-31Completed
INternational VErapamil SR Trandolapril STudy [NCT00133692]Phase 422,000 participants Interventional1997-09-30Completed
A Cross-over Trial to Identify Patient Characteristics That Predict Blood Pressure Response to Antihypertensive Therapy in General Practice [NCT00457483]Phase 4120 participants (Actual)Interventional2007-08-31Completed
A Multi-Center, Randomized, Proof-of-Concept, Parallel Control Study With Remind Cap® in Patients With Essential Hypertension and Newly Treated With Valsartan+/-Hydrochlorothiazide (HCTZ) [NCT00487123]Phase 40 participants InterventionalCompleted
A Phase III, Multicenter, Open-Label, Dose-Titrating, 16-Week Study Evaluating The Efficacy, Tolerability and Safety of Olmesartan Medoxomil 20 Mg and 40 Mg Alone or in Combination With 12.5 Mg to 25 Mg of Hydrochlorothiazide in Subjects With Mild to Mode [NCT00139698]Phase 3410 participants Interventional2005-09-30Completed
Effect of Licorice and Hydrochlorothiazide on Plasma Potassium [NCT00605202]Phase 410 participants (Actual)Interventional2008-02-29Completed
A Randomized, Double-blind, Parallel Group, Active-controlled Study to Compare the Systolic Blood Pressure Lowering Efficacy of Aliskiren, Ramipril and a Combination of Aliskiren and Amlodipine, With an Initial 8-week Evaluation, Followed by a 2-3 Year Fo [NCT01922141]Phase 40 participants (Actual)Interventional2015-05-31Withdrawn
Efficacy and Safety of Olmesartan: Reduction of Blood Pressure in the Treatment of Patients Suffering From Mild to Moderate Essential Hypertension [NCT00185172]Phase 32,333 participants (Actual)Interventional2002-01-31Completed
A Phase IV, Randomized, Open-Label, Active Controlled Study to Compare the Effects of Tarka® and Hyzaar® on Glucose Tolerance in Subjects With Metabolic Syndrome [NCT00234858]Phase 4280 participants (Actual)Interventional2004-03-31Completed
A Randomized Controlled Trial of Aliskiren in the Prevention of Major Cardiovascular Events in Elderly People [NCT01259297]Phase 32,336 participants (Actual)Interventional2011-01-31Terminated(stopped due to Terminated early in agreement with Health Authorities for feasibility reasons)
An Open-label, Long-term Extension Study to Evaluate the Safety, Tolerability and Efficacy of 12 Months of LCZ696 Treatment in Patients With Essential Hypertension [NCT01256411]Phase 2341 participants (Actual)Interventional2010-11-30Completed
Atrial Substrate Modification With Aggressive Blood Pressure Lowering to Prevent AF [NCT00438113]Phase 4184 participants (Actual)Interventional2009-12-31Completed
A Randomized, Open Label, Cross-over Comparative Study of Irbesartan/Hydrochlorothiazide and Irbesartan in the Treatment of Mild to Moderate Hypertension [NCT00443612]Phase 460 participants (Actual)Interventional2006-09-30Completed
A Multicenter, Open-label, 18 Month Study to Evaluate the Long-term Safety and Tolerability of Valsartan in Children 6 to 17 Years of Age With Hypertension and With or Without Chronic Kidney Disease [NCT01365481]Phase 3150 participants (Actual)Interventional2011-08-31Completed
A Comparative Study of the Efficacy of Irbesartan/Hydrochlorothiazide 300/25 mg Versus Valsartan/Hydrochlorothiazide 160/25 mg Using Home Blood Pressure Monitoring in the Treatment of Mild to Moderate Hypertension [NCT00500604]Phase 41,617 participants (Actual)Interventional2007-07-31Completed
A Randomized, Open-Label, Phase 3 Study to Compare Long-Term Safety and Tolerability of the TAK-491 and Chlorthalidone Fixed-Dose Combination Versus Olmesartan Medoxomil and Hydrochlorothiazide Fixed-Dose Combination in Hypertensive Subjects With Moderate [NCT01309828]Phase 3153 participants (Actual)Interventional2011-03-31Completed
An Open-Label, Randomized, Multicenter Study to Evaluate the Efficacy of the Combination of Valsartan and Hydrochlorothiazide and Amlodipine in Hypertensive Patients Not Controlled With Valsartan and Hydrochlorothiazide [NCT00400777]Phase 4460 participants (Anticipated)Interventional2006-08-31Completed
A Double Blind, Randomised, 3-Arm Parallel Group, Multicentre, 8-Week, Phase III Study to Assess Antihypertensive Efficacy and Safety of the Combination of Candesartan Cilexetil (CC) /HCT 32/12.5mg and 32/25mg vs. CC 32mg Alone in Patients With Inadequate [NCT00383929]Phase 31,979 participants (Actual)Interventional2006-09-30Completed
Double-blind, Randomized, Parallel Design Study Comparing Effectiveness of Losartan vs. Hydrochlorothiazide in Reversing or Preventing the Progression of the Remodeling of Resistance Arteries in Pre-hypertensive Pre-diabetic Subjects [NCT00388388]Phase 21 participants (Actual)Interventional2007-03-31Terminated(stopped due to Few subjects recruited, sponsor withdrew support.)
Action to Control Cardiovascular Risk in Diabetes (ACCORD) [NCT00000620]Phase 310,251 participants (Actual)Interventional1999-09-30Completed
Aldosterone and Vascular Disease in Diabetes Mellitus [NCT00214825]46 participants (Actual)Interventional2003-08-31Completed
A Randomised, Double-Blind, Placebo-Controlled, 3 x 3 Factorial Trial of Telmisartan and Hydrochlorothiazide in Patients With Essential Hypertension [NCT00153049]Phase 2583 participants (Actual)Interventional2004-06-30Completed
Comparison of the Combination of Valsartan 320 mg Plus Hydrochlorothiazide 12.5 mg and Valsartan 320 mg Plus Hydrochlorothiazide 25 mg to Valsartan 320 mg in Mild to Moderate Hypertensive Patients Not Adequately Controlled With Valsartan 320 mg [NCT00170989]Phase 32,714 participants (Actual)Interventional2004-09-30Completed
A Prospective, Open Label, Titration Study to Assess the Efficacy and Safety of Benicar® and Benicar ®HCT in Patients With Stage II Systolic Hypertension [NCT00185068]Phase 4110 participants Interventional2004-03-31Completed
Multi-Centre Olmesartan Atherosclerosis Regression Evaluation (MORE) [NCT00185185]Phase 3165 participants (Actual)Interventional2001-11-30Completed
The Pathophysiology and Treatment of Supine Hypertension in Patients With Autonomic Failure [NCT00223717]Phase 1152 participants (Actual)Interventional2001-01-31Completed
An Open Label, Randomized, 2-Period, 2-Treatment,2-Sequence, Crossover, Single-Dose BE of FDC of Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide Tab 40+10+25 mg [Torrent,India] Vs Tribenzor 40+10+25 mg Tablets [ Daichi,USA] in Healthy Subjects-Fe [NCT02962258]Phase 134 participants (Actual)Interventional2011-05-31Completed
Nephropathy in Type 2 Diabetes: Effects of an Intensive Multifactorial Intervention Trial on Cardio-renal Events. [NCT00535925]Phase 4850 participants (Actual)Interventional2005-10-31Completed
The Effect of Thiazide and Loop Diuretic on Mineral and Bone Disorder in Chronic Kidney Disease Patients [NCT03082742]52 participants (Anticipated)Interventional2015-08-01Recruiting
Black Education and Treatment of Hypertension (BEAT HTN) [NCT00661895]Phase 499 participants (Actual)Interventional2005-08-31Completed
A Twenty-four Week, Open-label, Non-comparative, Multi-center Study to Assess the Efficacy and Tolerability of an Aliskiren-based Treatment Algorithm in Patients With Mild to Moderate Hypertension. [NCT00765947]Phase 4256 participants (Actual)Interventional2008-09-30Completed
Specific Blockage of Angiotensine 2 and Podocyturia in Glomerular Nephropathies With Hypertension and Proteinuria [NCT00369538]Phase 420 participants (Anticipated)Interventional2006-08-31Suspended(stopped due to principle investigator moved, new investigators will join, insurance expired - project needs to be re-examined by an ethic committee)
A Translational Approach to Gitelman Syndrome [NCT00822107]8 participants (Actual)Interventional2009-01-31Completed
A Prospective Randomised Study to Compare a Fixed Dose Combination of Telmisartan 80 mg Plus Hydrochlorothiazide 25 mg With a Fixed Dose Combination of Telmisartan 80 mg Plus Hydrochlorothiazide 12.5 mg in Patients With Uncontrolled Hypertension Who Fail [NCT00239369]Phase 3713 participants Interventional2005-10-31Completed
A Study Comparing Valsartan With And Without Hydrochlorothiazide In Patients With Hypertension [NCT00241007]Phase 3836 participants (Actual)Interventional2003-12-31Completed
A Prospective, Randomised, Open-Label, Blinded-Endpoint, Parallel Group 6-week Treatment Study Comparing Telmisartan Combined With Hydrochlorothiazide (40 mg/12.5 mg or 80 mg/12.5 mg) Tablets With Losartan Combined With Hydrochlorothiazide (50 mg/12.5 mg) [NCT00274638]Phase 4805 participants (Actual)Interventional2002-07-31Completed
Behavioural Treatment of Hypertension [NCT00247910]150 participants (Actual)Interventional2001-10-31Completed
A Multicenter, Double-blind, Randomized, Active Controlled, Parallel Group Trial Comparing the Combinations of Valsartan 80 mg Plus Hydrochlorothiazide 12.5 mg to Valsartan 80 mg in Patients With Mild to Moderate Essential Hypertension Not Adequately Cont [NCT00250562]Phase 31,171 participants (Actual)Interventional2005-10-31Completed
A Randomized, Open Label Comparative Study of Irbesartan/Hydrochlorothiazide and Irbesartan in the Treatment of Mild to Moderate Hypertension [NCT00263003]Phase 340 participants Interventional2005-06-30Completed
Evaluation of a Primary Health Care Intervention for the Prevention of Cardiovascular Disease in Rural Andhra Pradesh [NCT00263393]Phase 43,712 participants (Actual)Interventional2005-12-31Completed
A Multicentre Prospective Randomized Open-Label 12-Week Study With Blinded Evaluation Comparing the Efficacy and Safety of Irbesartan and Irbesartan-Hydrochlorothiazide Fixed Combination With Amlodipine and Amlodipine Plus Hydrochlorothiazide in Elderly P [NCT00264212]Phase 4436 participants Interventional2004-08-31Completed
A Randomised Study Examining the Effect of Different Diuretics on Fluid Balance in Diabetics Treated With Avandia [NCT00306696]Phase 4388 participants (Actual)Interventional2002-10-31Completed
A 6-Week Study to Evaluate the Combination of Valsartan/HCTZ (160/12.5mg With Forced Titration to Maximum Dose of 320/25mg) Compared to Valsartan Monotherapy (160mg With Forced Titration to 320mg) as Initial Therapy in Patients With Severe Hypertension [NCT00273299]Phase 3607 participants (Actual)Interventional2005-11-30Completed
A 28-week, Multicenter Study to Evaluate the Effects of Valsartan/Hydrochlorothiazide (160/12.5 mg) in Comparison With Hydrochlorothiazide (25 mg) Monotherapy, for the Treatment of Patients With Hypertension, Uncontrolled by Hydrochlorothiazide (12.5 mg) [NCT00277472]Phase 4300 participants (Actual)Interventional2005-11-30Completed
A Randomised Controlled Cross-over Trial to Evaluate Evening Versus Morning Administration of a Cardiovascular Polypill [NCT01506505]78 participants (Actual)Interventional2012-07-31Completed
The Relationship Between Serine Threonine Kinase 39 (STK39) Genotypes, Salt Sensitivity, Thiazide Diuretics-induced Blood Pressure Response [NCT00896389]Phase 4124 participants (Actual)Interventional2009-10-31Completed
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Irbesartan / Hydrochlorothiazide 300/25 mg Tablets Under Fed Conditions [NCT01712126]40 participants (Actual)Interventional2007-09-30Completed
A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Irbesartan / Hydrochlorothiazide 300/25 mg Tablets Under Fasting Conditions [NCT01712139]37 participants (Actual)Interventional2007-09-30Completed
Creating an Active Collaborative Network of Comparative Effectiveness Researchers: A Randomized Study of Initial Diuretic Therapy for Hypertension. [NCT01748123]Phase 40 participants (Actual)Interventional2016-08-31Withdrawn(stopped due to Slow enrollment)
Pharmacokinetic Interactions of Valsartan and Hydrochlorothiazide: An Open-Label, Randomized, Four-Period Crossover Study in Healthy Egyptian Male Volunteers [NCT01767259]24 participants (Actual)Interventional2012-10-31Completed
Pharmacokinetic Interactions of Valsartan and Hydrochlorothiazide: An Open-Label, Randomized, Four-Period Crossover Study in Healthy Egyptian Male Volunteers (PART II) [NCT01767298]24 participants (Actual)Interventional2012-10-31Completed
ENaC as a Novel Mechanism for Hypertension and Volume Expansion in Type 2 Diabetes [NCT01804777]Early Phase 19 participants (Actual)Interventional2013-03-31Terminated(stopped due to Currently closed for data analysis.)
[NCT01819220]Phase 416 participants (Actual)Interventional2009-04-30Completed
Azelnidipine vs Perindopril and Stratification of Blood Pressure Control Against Progress of Cerebral Small Vessel Diseases in Poststroke Patients (APPROVE):Multi-center Randomized Controlled Clinical Trial [NCT01819441]Phase 41,200 participants (Anticipated)Interventional2012-05-31Recruiting
The Effect of Chlorthalidone Compared to Hydrochlorothiazide on Endothelial Function in Hypertensive Patients: A Pilot Study [NCT01822860]Phase 40 participants (Actual)Interventional2013-03-31Withdrawn(stopped due to Study subjects were not able to be recruited)
A Randomized, Open Label, Balanced, Two-Treatment, Two-Period, Two-Sequence, Single Dose, Crossover, Comparative Bioavailability Study of Lisinopril and Hydrochlorothiazide Tablets (20+25) mg of M/s Ipca Laboratories Ltd., India With Zestoretic® 20/25 Lis [NCT01827878]Phase 148 participants (Actual)Interventional2012-10-31Completed
Safety and Efficacy of the Combination of Loop Diuretics With Thiazide-type Diuretics in Patients With Decompensated Heart Failure: a Double-blind, Randomized, Placebo-controlled Trial (CLOROTIC Trial). [NCT01647932]Phase 3232 participants (Actual)Interventional2014-10-31Completed
A Randomized, Double-Blind, Multicenter, Parallel Study Evaluating the Efficacy and Safety of a Combination of Ramipril Plus Hydrochlorothiazide Versus the Component Monotherapies in Subjects With Essential Hypertension [NCT00355589]Phase 30 participants Interventional2006-07-31Completed
Clinical Assessment Of Association Pharmacokinetics Atorvastatin + Losartana + Hydrochlorothiazide Produced By Lab Hypermarcas S/A In Healthy Subjects [NCT01692717]Phase 190 participants (Actual)Interventional2013-02-28Completed
Observational Study in Everyday Medical Practice of the Effectiveness of Telmisartan for Treatment of Isolated Systolic Hypertension in Comparison With Systolic/Diastolic Hypertension in Patients Aged 55 or Older [NCT02242877]3,320 participants (Actual)Observational2006-02-28Completed
Clinical Trial to Compare the Pharmacokinetics of TAH Tablet(80/10/12.5mg) in Comparison to the Co-administration of Telmisartan, Amlodipine and Hydrochlorothiazide in Healthy Male Volunteers [NCT03032315]Phase 144 participants (Actual)Interventional2016-10-01Completed
National, Multicenter, Open-Label and Prospective Study Assessment of Efficacy and Safety in Stage 1 and 2 Essential Hypertension With Olmesartan Medoxomil Based Treatment Algorithm From Monotherapy to Association With Hydrochlorothiazide and Amlodipine B [NCT00890591]Phase 4144 participants (Actual)Interventional2006-08-31Completed
Efficacy and Safety Evaluation of the New Association on Fixed Dose of Olmesartan Medoxomil + Chlorthalidone (40mg + 12.5mg and 40mg + 25mg) Compared With BENICAR HCT® in Hypertension Control [NCT02483936]Phase 3348 participants (Anticipated)Interventional2023-04-30Not yet recruiting
The CORONAvirus Disease 2019 Angiotensin Converting Enzyme Inhibitor/Angiotensin Receptor Blocker InvestigatiON (CORONACION) Randomized Clinical Trial [NCT04330300]Phase 42,414 participants (Anticipated)Interventional2020-04-30Suspended(stopped due to Challenges with funding and very low incidence of COVID-19 at Irish study site)
Randomized, Phase 3, Multicenter, Open Label, Evaluating the Effect of the Treatment of Indapamide 1.5mg/Losartan 50mg and Indapamide 1.5mg/Losartan 100mg, Compared With Hyzaar® in the Treatment of Hypertension [NCT01620788]Phase 3636 participants (Anticipated)Interventional2019-11-27Suspended(stopped due to Substancial amendment)
Multimodal Intervention to Reduce Cardiovascular Risk Among Hypertensive Older Adults [NCT01891513]104 participants (Actual)Observational2014-01-31Completed
Peripheral Vascular Effects of Sulfhydryl-containing Antihypertensive Pharmacotherapy on Microvascular Function and Vessel Remodeling in Hypertensive Humans [NCT03179163]Phase 1/Phase 246 participants (Actual)Interventional2016-07-20Terminated(stopped due to COVID shut down human subjects research and then the grant funding expired)
An Open-label, Multicenter Study to Evaluate the Efficacy and Tolerability of a 4 Week Therapy With the Fixed Dose Combination of Valsartan 160 mg Plus HCTZ 25 mg in Hypertensive Patients Not Adequately Responding to a 4 Week Therapy With the Free Combina [NCT00360178]Phase 3198 participants (Actual)Interventional2006-07-31Completed
Data Analysis for Drug Repurposing for Effective Alzheimer's Medicines (DREAM)- Dihydropyridine Calcium Channel Blockers Versus Hydrochlorothiazide [NCT05125224]163,720 participants (Actual)Observational2021-10-01Active, not recruiting
A Randomized, Open-label Study to Evaluate the Effects on Blood Pressure Control, Pulse Wave Velocity, as Well as Safety and Tolerability of Felodipine Sustained Release, Alone and in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide, in Chin [NCT02336607]529 participants (Actual)Interventional2005-12-31Completed
Use of Hydrochlorothiazide and the Risk of Skin Cancer [NCT04334824]2,953,748 participants (Actual)Observational2019-05-27Completed
CSP #597 - Diuretic Comparison Project [NCT02185417]Phase 313,523 participants (Actual)Interventional2016-06-15Completed
An Open-Label, Long-term (52-week), Safety Trial of the Fixed Dose Combination of Telmisartan 80mg Plus Hydrochlorothiazide 12.5mg and Telmisartan 40mg Plus Hydrochlorothiazide 12.5mg in Patients With Essential Hypertension - Efficacy and Safety Evaluatio [NCT00326768]Phase 3184 participants (Actual)Interventional2006-05-31Completed
A 10-week Multicenter,Forced-titration Study Using 24-hr ABPM to Evaluate the Efficacy of Valsartan/Hydrochlorothiazide (HCTZ) Treatment Regimen vs Conventional Treatment Regimen With Amlodipine and Hydrochlorothiazide (HCTZ) in Patients With Stage 2 Hype [NCT00425997]Phase 4480 participants (Anticipated)Interventional2006-12-31Completed
An 8-week, Multicenter Study to Evaluate the Efficacy and Safety of the Combination of Valsartan/HCTZ/Amlodipine Compared to Valsartan/HCTZ, Valsartan/Amlodipine, and HCTZ/Amlodipine in Patients With Moderate to Severe Hypertension. [NCT00327587]Phase 32,279 participants (Actual)Interventional2006-05-31Completed
Randomized Double-blind Placebo-controlled Trial Assessing the Efficacy of Standard and Low Dose Hydrochlorothiazide Treatment in the Prevention of Recurrent Nephrolithiasis [NCT03057431]Phase 3416 participants (Actual)Interventional2017-03-09Completed
Vascular Dysfunction in Human Obesity Hypertension: Integrative Role of Sympathetic and Renin-Angiotensin Systems [NCT01983462]Phase 233 participants (Actual)Interventional2013-10-31Terminated(stopped due to Funding expired)
Protocol H8D-MC-EMBH PPAR Alpha (LY518674): a Phase 2 Dose-Response Study to Evaluate the Blood Pressure-Lowering Effect in Essential Hypertension [NCT00374855]Phase 2153 participants Interventional2006-09-30Completed
An Open Label Study to Assess the Efficacy of Losartan/HCTZ Combination Therapy in Patients With Essential Hypertension Who Were Inadequately Controlled on Current Antihypertensive Monotherapy [NCT00354991]Phase 3437 participants (Actual)Interventional2006-06-01Completed
Efficacy and Safety of the Combination of Benazepril Plus Hydrochlorothiazide in Chinese Patients With Mild to Moderate Essential Hypertension Not Adequately Controlled With Benazepril [NCT00367094]Phase 3296 participants Interventional2006-07-31Completed
Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) [NCT00246519]Phase 41,701 participants (Actual)Interventional2005-10-31Completed
Pharmacologic Treatment of Congenital Nephrogenic Diabetes Insipidus [NCT00478335]4 participants (Actual)Interventional2007-05-31Completed
A 12 Week, Double-blind, Randomized, Parallel Group, Multi-center Study to Evaluate the Efficacy and Safety of the Combination of Aliskiren 300 mg and Hydrochlorothiazide 25 mg Compared to Aliskiren 300 mg in Patients With Stage II Hypertension [NCT00705575]Phase 3688 participants (Actual)Interventional2008-06-30Completed
Effects on Blood Pressure and Central Sympathetic Nerve Traffic by SGLT2-inhibition With Empagliflozin Compared to Hydrochlorothiazide in Patients With Type 2 Diabetes Mellitus [NCT03254849]Phase 475 participants (Actual)Interventional2017-12-08Completed
Confirmatory Study of the Efficacy and Safety of the Combination of Losartan / Chlorthalidone vs Losartan / Hydrochlorothiazide in the Treatment of Patients With Essential Arterial Hypertension [NCT04927299]Phase 3190 participants (Anticipated)Interventional2022-06-30Recruiting
Single-center, Randomized, Open-label, Parallel-group Study to Characterize Renin-angiotensin-system (RAS) Peptide Profiles Before and After Treatment Initiation With Different Antihypertensive Drug-classes in Patients With Treatment-naive Arterial Hypert [NCT02449811]107 participants (Actual)Observational2015-04-30Completed
Effects and Safety of Sacubitril/Valsartan Versus Valsartan on Refractory Hypertension: The EOSORH Trial [NCT05545059]Phase 3138 participants (Anticipated)Interventional2022-09-24Recruiting
Lowering Blood Pressure in Primary Care in Vienna [NCT02377661]Phase 4229 participants (Actual)Interventional2015-03-31Completed
A Placebo Controlled Double Blinded Crossover Study of the Antihypertensive Efficacy of Guanfacine vs Hydrochlorothiazide in Obstructive Sleep Apnea (OSA) Associated Hypertension [NCT02699125]Phase 441 participants (Actual)Interventional2015-01-31Completed
An Eight-week Randomised Double-blind Study to Compare the Efficacy and Safety of Telmisartan 80 mg and Amlodipine 5 mg and Hydrochlorothiazide 12.5 mg vs. Telmisartan 80 mg and Amlodipine 5 mg in Patients With Hypertension Who Fail to Respond Adequately [NCT01975246]Phase 3309 participants (Actual)Interventional2013-11-30Completed
Characterization of Arterial Hypertension and Efficacy of Blood-pressure Lowering Therapy at Different Altitudes Above Sea Level [NCT02373163]Phase 4120 participants (Anticipated)Interventional2014-09-30Recruiting
A Phase I, Randomized, Double-Blind, Placebo-hydrochlorothiazide Parallel Controlled, Multiple-Ascending Dose Study to Evaluate the Safety, Efficacy of SHR 0532 Oral Tablets in Mild Hypertension Subjects [NCT03971929]Phase 136 participants (Actual)Interventional2019-07-31Completed
A 12 Week, Open, Randomized, Parallel, Multicenter Study of Efficacy, Tolerability & Safety of Hydrochlorothiazide (+) Losartan Potassium Versus Amlodipine in Essential Hypertensive Patients. [NCT00157963]Phase 4174 participants (Actual)Interventional2005-02-05Completed
A Randomized, Open Label, Balanced, Two-Treatment, Two-Period, Two-Sequence, Single Dose, Crossover, Comparative Bioavailability Study of Lisinopril and Hydrochlorothiazide Tablets (20+25) mg of M/s Ipca Laboratories Ltd., India With Zestoretic® 20/25 Lis [NCT01831700]Phase 148 participants (Actual)Interventional2012-10-31Completed
A Pilot Study of Plasma Renin Activity Guided vs Generic Combination Therapy for Hypertension [NCT01658657]17 participants (Actual)Interventional2012-10-31Completed
Generation of Biological Samples Positive to Hydrochlorothiazide for Anti-doping Control [NCT04197622]Phase 13 participants (Actual)Interventional2019-03-05Completed
Efficacy and Safety Evaluation of the New Association on Fixed Dose of Olmesartan + Chlorthalidone, Produced by EMS S.A,in Arterial Hypertension Control [NCT02493322]Phase 3261 participants (Anticipated)Interventional2023-04-30Not yet recruiting
Efficacy and Safety of a Single-pill Fixed Combination of Sufficient Losartan/Hydrochlorothiazide in Chinese Hypertensive Patients (FOCUS) [NCT03946514]Phase 4300 participants (Anticipated)Interventional2018-09-01Recruiting
Effect of Aliskiren 300mg and Hydrochlorothiazide 25mg on Kidney Oxygenation in Patients With Stage 1 and 2 Hypertension: a BOLD-MRI Study [NCT01519635]Phase 424 participants (Actual)Interventional2011-10-31Completed
HYDROchlorothiazide to PROTECT Polycystic Kidney Disease Patients and Improve Their Quality of Life [NCT05373264]Phase 3300 participants (Anticipated)Interventional2024-03-31Not yet recruiting
Mechanisms of Reduced Ramipril on the Onset of Type 2 Diabetes Mellitis [NCT00574834]Early Phase 117 participants (Actual)Interventional2007-03-31Terminated(stopped due to Lack of funding)
Changes in Central Aortic Pressure, Endothelial Function and Biomarkers in African Americans With Cardiometabolic Syndrome: Comparison of Amlodipine/Olmesartan Versus Hydrochlorothiazide/Losartan [NCT01271374]Phase 480 participants (Anticipated)Interventional2010-04-30Active, not recruiting
Investigation of Pharmacodynamic and Pharmacokinetic Interactions Between 25 mg BI 10773 and 25 mg Hydrochlorothiazide or 5 mg Torasemide Under Steady State Conditions in Patients With Type 2 Diabetes Mellitus in an Open-label, Randomised, Cross-over Tria [NCT01276288]Phase 123 participants (Actual)Interventional2011-01-31Completed
A Randomized, Double-blind 52-week Study to Evaluate the Safety and Efficacy of an LCZ696 Regimen Compared to an Olmesartan Regimen on Arterial Stiffness Through Assessment of Central Blood Pressure in Elderly Patients With Hypertension [NCT01692301]Phase 2454 participants (Actual)Interventional2012-12-31Completed
A Study of a Hypertensive Population Under Treatment With Micardis® and Micardis Plus® Under Real Clinical Conditions With the Goal to Control the Early Morning BP Rise (SURGE II) [NCT02242396]5,248 participants (Actual)Observational2005-08-31Completed
Morning Hypertension and Patient Self-monitoring [NCT02243566]2,707 participants (Actual)Observational2006-04-30Completed
The Standardized and Economical Mode for the Prevention and Management of Chronic Cardiovascular Diseases: Matrix System From Rural Shaanxi ( MATRIX ) Ⅰ [NCT04371874]1,210 participants (Actual)Interventional2014-01-31Completed
Randomized Controlled Blind End Point Study of Enalapril Folic Acid Tablets Combined With Calcium Antagonist or Diuretic to Prevent Stroke in Patients With Type H Hypertension [NCT04952051]Phase 31,000 participants (Actual)Interventional2014-07-01Completed
Improving Pain Management Via Spinal Cord Stimulation and Blood Pressure Reduction (PASSION Study) [NCT04676399]Early Phase 136 participants (Anticipated)Interventional2022-02-08Recruiting
An Eight-week Randomised Double-blind Study to Compare the Efficacy and Safety of Telmisartan 80 mg and Amlodipine 5 mg and Hydrochlorothiazide 12.5 mg vs. Telmisartan 80 mg and Hydrochlorothiazide 12.5 mg in Patients With Hypertension Who Fail to Respond [NCT01911780]Phase 3132 participants (Actual)Interventional2013-07-31Completed
The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC Trial) [NCT00605072]Phase 253 participants (Actual)Interventional2008-01-31Completed
Pharmaco-epidemiological Study Describing a Population of Hypertensive Patients Treated in General Practice With a Fixed-dose Combination of Telmisartan and Hydrochlorothiazide, the Level of Blood Pressure Control and the Modalities of Arterial Hypertensi [NCT02248129]4,255 participants (Actual)Observational2006-04-30Completed
Randomized, Double-blind, Crossover Trial Assessing the Efficacy of Indapamide and Chlorthalidone Compared to Hydrochlorothiazide for the Reduction of Urine Supersaturation for Kidney Stone Prevention [NCT06111885]Phase 299 participants (Anticipated)Interventional2024-04-30Not yet recruiting
Furosemide With Early Sequential Nephron Blockade Versus Furosemide Alone in Acute Heart Failure Patients With Furosemide-guided Diuretic Resistance: A Double-blinded, Randomized, Placebo-controlled Study [NCT04465123]Phase 3100 participants (Anticipated)Interventional2020-08-13Recruiting
Dapagliflozin Effect on Erythropoiesis and Physical Fitness in Patients With Type 2 Diabetes - a Randomized, Partly Double-blinded, Controlled, Three Armed, Parallel Group, Exploratory Study [NCT03423355]Phase 40 participants (Actual)Interventional2021-09-30Withdrawn(stopped due to change in sponsor)
Pharmacokinetics of Multiple Oral Doses of Telmisartan 80 mg/Amlodipine 5 mg/Hydrochlorothiazide 12.5 mg Fixed-dose Combination Tablet, Telmisartan 80 mg/Hydrochlorothiazide 12.5 mg Fixed-dose Combination Tablet and Telmisartan 80 mg/Amlodipine 5 mg Fixed [NCT02183675]Phase 136 participants (Actual)Interventional2014-07-31Completed
The SCCS Polypill Pilot Trial [NCT02278471]Phase 2303 participants (Actual)Interventional2015-12-31Completed
Series of N-of-1 Crossover Trials of Antihypertensive Therapy in Adolescents With Essential Hypertension [NCT02412761]42 participants (Actual)Interventional2013-06-30Completed
ECARD Combination Tablets LD&HD Special Drug Use Surveillance: Long-term Use (12 Months) [NCT02016183]3,222 participants (Actual)Observational2009-04-01Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00000620 (6) [back to overview]Death From Any Cause in the Glycemia Trial.
NCT00000620 (6) [back to overview]First Occurrence of a Major Cardiovascular Event (MCE); Specifically Nonfatal Heart Attack, Nonfatal Stroke, or Cardiovascular Death (Measured Throughout the Study) in the Glycemia Trial.
NCT00000620 (6) [back to overview]First Occurrence of Major Cardiovascular Event (MCE) in the Blood Pressure Trial.
NCT00000620 (6) [back to overview]First Occurrence of Major Cardiovascular Event (MCE) in the Lipid Trial.
NCT00000620 (6) [back to overview]First Occurrence of MCE or Revascularization or Hospitalization for Congestive Heart Failure (CHF) in Lipid Trial.
NCT00000620 (6) [back to overview]Stroke in the Blood Pressure Trial.
NCT00170950 (3) [back to overview]Time-to-event Analysis of Percentage of Patients With a Cardiovascular (CV) Mortality Event, Non-fatal Myocardial Infarction (MI), or Non-fatal Stroke
NCT00170950 (3) [back to overview]Time-to-event Analysis of Percentage of Patients With a Composite Cardiovascular (CV) Morbidity or Mortality Event
NCT00170950 (3) [back to overview]Time-to-event Analysis of Percentage of Patients With a Composite Cardiovascular (CV) Morbidity Event
NCT00171054 (13) [back to overview]Change From Baseline to Week 38 in the Carotid-femoral Pulse Wave Velocity (PWV)
NCT00171054 (13) [back to overview]Changes in Mean Right Carotid Distensibility at Week 38
NCT00171054 (13) [back to overview]Changes in Mean Right Carotid Distensibility at Week 12
NCT00171054 (13) [back to overview]Change in Left Ventricular Mass Index (LVMI) and Diastolic Function Using Echocardiography From Baseline to Week 38
NCT00171054 (13) [back to overview]Changes in Baroreflex Sensitivity as it Relates to Changes in Carotid Distensibility From Baseline to Week 12
NCT00171054 (13) [back to overview]Change From Baseline for Endothelial Function Measured by Brachial Artery Flow-mediated Vasodilatation (FMD) Using the Brachial Artery Reactivity Test (BART) at Week 12
NCT00171054 (13) [back to overview]Changes in Mean Left Carotid Distensibility at Week 12
NCT00171054 (13) [back to overview]Change From Baseline for Endothelial Function Measured by Brachial Artery Flow-mediated Vasodilatation (FMD) Using the Brachial Artery Reactivity Test (BART) at End-point (Week 38)
NCT00171054 (13) [back to overview]Changes in Baroreflex Sensitivity as it Relates to Changes in Carotid Distensibility From Baseline to Week 38
NCT00171054 (13) [back to overview]Changes in Mean Left Carotid Distensibility at Week 38
NCT00171054 (13) [back to overview]Changes in Central Blood Pressure, Evaluated by Applanation Tonometry From Baseline at Weeks 12 and 38
NCT00171054 (13) [back to overview]Change From Baseline in Post-ischemic Forearm Skin Reactive Hyperemia at Endpoint (Week 38)
NCT00171054 (13) [back to overview]Change From Baseline in Post-ischemic Forearm Skin Reactive Hyperemia at Week 12
NCT00246519 (1) [back to overview]Blood Pressure Response (Delta BP (After 18 Weeks of Medication - Baseline)).
NCT00311155 (6) [back to overview]Mean Change in Diastolic Blood Pressure Overall and for Each Treatment From Baseline to the Completion of the Treatment
NCT00311155 (6) [back to overview]Mean Change in Systolic Blood Pressure Overall and for Each Treatment From Baseline to the Completion of the Treatment
NCT00311155 (6) [back to overview]Percentage of Participants Who Achieved Normalized Blood Pressure Overall and for Each Treatment From Baseline to Completion of the Treatment During Which Blood Pressure Goals Were Achieved
NCT00311155 (6) [back to overview]Percentage of Participants Who Were Diastolic Responders Overall and for Each Treatment From Baseline to the Completion of Treatment During Which Blood Pressure Goals Were Achieved.
NCT00311155 (6) [back to overview]Percentage of Participants Who Were Systolic Responders Overall and for Each Treatment From Baseline to the Completion of the Treatment During Which Blood Pressure Goals Were Achieved
NCT00311155 (6) [back to overview]The Percentage of Participants Treated to Target Blood Pressure Goals Overall and for Each Treatment Step From Baseline to Completion of Treatment During Which the Goal Was Achieved.
NCT00368277 (4) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure to Week 12
NCT00368277 (4) [back to overview]Percentage of Patients Achieving Blood Pressure Control at Weeks 12 and 36 Endpoints
NCT00368277 (4) [back to overview]Percentage of Patients With Cough
NCT00368277 (4) [back to overview]Change From Baseline in the Mean Sitting Diastolic Blood Pressure to Week 36
NCT00386607 (8) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure
NCT00386607 (8) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure.
NCT00386607 (8) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure.
NCT00386607 (8) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure
NCT00386607 (8) [back to overview]Overall Percentage of Patients With Adverse Events
NCT00386607 (8) [back to overview]Overall Percentage of Patients With Adverse Events
NCT00386607 (8) [back to overview]Percentage of Patients Achieving Blood Pressure Control Target of < 140/90 mmHg in Extension Treatment
NCT00386607 (8) [back to overview]Percentage of Patients Achieving Blood Pressure Control Target of < 140/90 mmHg
NCT00396656 (6) [back to overview]Mean Post-treatment Microcirculation at NaCl Injected Sites
NCT00396656 (6) [back to overview]Difference in Mean Post-treatment Microcirculation at Acetylcholine (ACH) Plus L-NMMA Injected Sites Compared to NaCl Injected Sites
NCT00396656 (6) [back to overview]Difference in Mean Post-treatment Microcirculation at Acetylcholine (ACH) Injected Sites Compared to NaCl Injected Sites
NCT00396656 (6) [back to overview]Difference in Mean Post-treatment Microcirculation at a Sodium Nitroprusside Injected Site Compared to NaCl Injected Sites
NCT00396656 (6) [back to overview]Arterial Pressure Waveform Augmentation Index at the End of Treatment
NCT00396656 (6) [back to overview]Arterial Pressure Waveform Pulse Wave Velocity at the End of Treatment
NCT00402103 (4) [back to overview]Overall Percentage of Patients With Adverse Events
NCT00402103 (4) [back to overview]Percentage of Patients Achieving a Response in Mean Sitting Diastolic Blood Pressure (msDBP)
NCT00402103 (4) [back to overview]Percentage of Patients Achieving a Blood Pressure Control Target of <140/90 mmHg
NCT00402103 (4) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP)From Baseline to the Indicated Time Points
NCT00403481 (9) [back to overview]Change From Baseline to Week 12 in Ambulatory BP Measurement (Systolic)During the Last 2 Hours of the Last (Week 12) 24-hour Dosing Period.
NCT00403481 (9) [back to overview]Change From Baseline to Week 12 in Ambulatory BP Measurement (Systolic)During the Last 4 Hours of the Last (Week 12 ) 24-hour Dosing Period.
NCT00403481 (9) [back to overview]Change From Baseline to Week 12 in Ambulatory BP Measurement (Systolic)During the Last 6 Hours of the Last (Week 12 ) 24-hour Dosing Period.
NCT00403481 (9) [back to overview]Change From Baseline to Week 12 in Mean 24-hour Ambulatory BP (Diastolic)
NCT00403481 (9) [back to overview]Change From Baseline to Week 12 in Systolic BP (SBP) as Measured by 24-hour ABPM.
NCT00403481 (9) [back to overview]Change in Ambulatory Blood Pressure (Diastolic) From Baseline to Week 12 During the Last 2 Hours of the Last (Week 12 ) 24-hour Dosing Period.
NCT00403481 (9) [back to overview]Change From Baseline to Week 12 in Mean Daytime and Nighttime Ambulatory Blood Pressure Measurement (Systolic).
NCT00403481 (9) [back to overview]Change in Daytime and Nighttime Ambulatory Blood Pressure (Diastolic) From Baseline to Week 12
NCT00403481 (9) [back to overview]Change in Ambulatory BP (Diastolic) From Baseline to Week 12 During the Last (Week 12 ) 4 and 6 Hours of the Last 24-hour Dosing Period.
NCT00412932 (7) [back to overview]Number of Subjects Who Achieved Mean Nighttime (10pm - 6am) Ambulatory Blood Pressure of <140/90 mm Hg, Systolic Blood Pressure <140 mm Hg, and Diastolic Blood Pressure <90 mm Hg After 12 Weeks of Active Treatment.
NCT00412932 (7) [back to overview]Change From Baseline in Mean 24-hour Ambulatory Diastolic Blood Pressure After 12 Weeks of Active Treatment.
NCT00412932 (7) [back to overview]Change From Baseline in Mean 24-hour Ambulatory Systolic Blood Pressure After 12 Weeks of Active Treatment
NCT00412932 (7) [back to overview]Change From Baseline in Mean Daytime (8am-4pm) and Mean Nighttime (10 Pm-6am) Ambulatory Blood Pressure Monitored Diastolic Blood Pressure After 12 Weeks of Active Treatment
NCT00412932 (7) [back to overview]Change From Baseline in Mean Daytime (8am-4pm) and Mean Nighttime (10pm-6am)Ambulatory Systolic Blood Pressure After 12 Weeks of Active Treatment
NCT00412932 (7) [back to overview]Number of Subjects Who Achieved Mean 24-hour Ambluatory Blood Pressure of <140/90 mm Hg, Systolic Blood Pressure <140 mm Hg, and Diastolic Blood Pressure <90 mm Hg After 12 Weeks of Active Treatment
NCT00412932 (7) [back to overview]Number of Subjects Who Achieved Mean Daytime (8am - 4pm) Ambulatory Blood Pressure of <140/90 mm Hg, Systolic Blood Pressure <140 mm Hg, and Diastolic Blood Pressure <90 mm Hg After 12 Weeks of Active Treatment.
NCT00430508 (8) [back to overview]Change in Mean Trough Sitting Systolic Blood Pressure From Week 8(Baseline) to Week 12.
NCT00430508 (8) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 16
NCT00430508 (8) [back to overview]Change in Mean Trough Sitting Systolic Blood Pressure From Week 8(Baseline) to Week 16.
NCT00430508 (8) [back to overview]Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 16
NCT00430508 (8) [back to overview]Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 12.
NCT00430508 (8) [back to overview]Change in Mean Night-time Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16.
NCT00430508 (8) [back to overview]Change in Mean Daytime Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16.
NCT00430508 (8) [back to overview]Change in Mean 24-hour Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16.
NCT00430638 (10) [back to overview]Change From Baseline in Mean Diastolic Blood Pressure (DBP) After 12 Weeks of Randomized Treatment as Measured by Omron Device.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Black Participants.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Females.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Males.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Non-Black Participants.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Participants Greater Than or Equal to 65 Years Old.
NCT00430638 (10) [back to overview]Change From Baseline in Mean Systolic Blood Pressure (SBP) After 12 Weeks of Randomized Treatment as Measured by Omron Device.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Participants Less Than 65 Years Old.
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Stage 1 Hypertensives
NCT00430638 (10) [back to overview]The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Stage 2 Hypertensives
NCT00430950 (5) [back to overview]Change in Mean Trough Sitting Diastolic Blood Pressure
NCT00430950 (5) [back to overview]Number of Participants Achieving Blood Pressure Goal.
NCT00430950 (5) [back to overview]Change in Sitting Systolic Blood Pressure 4 Weeks and 8 Weeks After Baseline.
NCT00430950 (5) [back to overview]Change in Daytime, Nighttime and 24-hour Blood Pressure Evaluated by Ambulatory Blood Pressure Monitoring 8 Weeks After Baseline.
NCT00430950 (5) [back to overview]Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 12
NCT00434967 (3) [back to overview]Change in Sitting Systolic Blood Pressure (SBP) From Baseline to the End of the Study (Baseline to 8 Weeks)
NCT00434967 (3) [back to overview]The Number of Patients With Controlled Sitting DBP and Sitting SBP in Each Treatment Group at the End of the Study
NCT00434967 (3) [back to overview]Change in Sitting Diastolic Blood Pressure (DBP) From Baseline to the End of the Study (From Baseline to 8 Weeks).
NCT00439738 (7) [back to overview]Change From Baseline in Postprandial Non-esterified Fatty Acids
NCT00439738 (7) [back to overview]Change in Mean Sitting Systolic Blood Pressure (MSSBP)
NCT00439738 (7) [back to overview]Number of Patients Achieving Blood Pressure (BP)Control by Visit (< 130/80 mm Hg)
NCT00439738 (7) [back to overview]Change From Baseline in Postprandial Glucose
NCT00439738 (7) [back to overview]Change From Baseline in Postprandial Insulin
NCT00439738 (7) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (MSDBP)
NCT00439738 (7) [back to overview]Number of Patients Achieving Blood Pressure (BP) Control by Visit (< 140/90 mm Hg)
NCT00446563 (15) [back to overview]Change From Baseline to End of Study in Levels of N-terminal Pro-B Type Natriuretic Peptide (NT-proBNP)
NCT00446563 (15) [back to overview]Change From Baseline to End of Study in Levels of High-sensitivity C-reactive Protein (Hs-CRP)
NCT00446563 (15) [back to overview]Change From Baseline in Left Ventricular Mass Index (LVMI) Measured Via Magnetic Resonance Imaging (MRI)
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Interventricular Septum Thickness (IVS) Assessed by MRI
NCT00446563 (15) [back to overview]Percentage of Participants Who Experienced Adverse Events (AEs)
NCT00446563 (15) [back to overview]Percentage of Participants Achieving Target Blood Pressure at Week 52
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Atrial (LA) Area Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in the Ascending Aortic Diameter Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Ventricular End-Systolic Volume (LVESV) Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Posterior Wall Thickness Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Ventricular End-diastolic Volume (LVEDV) Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Ventricular Ejection Fraction (LVEF) Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Ventricular End-diastolic Volume (LVEDV) Normalized to Body Surface Area Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Ventricular End-Systolic Volume (LVESV) Normalized to Body Surface Area Assessed by MRI
NCT00446563 (15) [back to overview]Change From Baseline to the End of Study in Left Ventricular Mass Index (LVMI) Normalized to Body Surface Area Assessed by MRI
NCT00459056 (1) [back to overview]Change in Reactive Hyperemic Index by Period (Carvedilol CR + Lisinopril vs. Lisinopril + HCTZ)
NCT00478335 (1) [back to overview]24h Urine Volume
NCT00496834 (4) [back to overview]Diastolic Blood Pressure (DBP) Mean Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug
NCT00496834 (4) [back to overview]Pulse Wave Velocity (PWV) Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug
NCT00496834 (4) [back to overview]PWV Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug
NCT00496834 (4) [back to overview]Systolic Blood Pressure (SBP) Mean Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug
NCT00523744 (12) [back to overview]Percentage of Patients Who Achieved Normalized Blood Pressure During the Extension Phase of the Study
NCT00523744 (12) [back to overview]Percentage of Patients Who Achieved Normalized Blood Pressure During the Core Phase of the Study
NCT00523744 (12) [back to overview]Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Extension Phase of the Study
NCT00523744 (12) [back to overview]Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Core Phase of the Study
NCT00523744 (12) [back to overview]Change in Sitting Pulse Rate During the Extension Phase of the Study
NCT00523744 (12) [back to overview]Change in Sitting Pulse Rate During the Core Phase of the Study
NCT00523744 (12) [back to overview]Change in Sitting Pulse Pressure During the Extension Phase of the Study
NCT00523744 (12) [back to overview]Change in Sitting Pulse Pressure During the Core Phase of the Study
NCT00523744 (12) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Extension Phase of the Study
NCT00523744 (12) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Core Phase of the Study
NCT00523744 (12) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Extension Phase of the Study
NCT00523744 (12) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Core Phase of the Study
NCT00535925 (2) [back to overview]"Number of Participants With Overall Fatal and Non-fatal, Major Adverse Cardiovascular Events (MACEs)"
NCT00535925 (2) [back to overview]"Number of Participants Who Achieved of BP, HbA1c and Total, HDL and LDL Cholesterol Goals at the End of Intervention Phase"
NCT00546052 (13) [back to overview]Change in Body Mass Index Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Absolute Change in C Reactive Protein Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Absolute Change in Uric Acid Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Target Blood Pressure
NCT00546052 (13) [back to overview]Percent Change in Triglycerides Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Percent Change in Total Cholesterol Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Percent Change in Low Density Lipoprotein-C Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Percent Change in High Density Lipoprotein-C Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Change in Waist Circumference Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Change in Systolic Blood Pressure Between Baseline and 52 Week Assessments
NCT00546052 (13) [back to overview]Change in Hemoglobin A1c Between 52 Weeks and Baseline
NCT00546052 (13) [back to overview]Change in Fasting Blood Glucose Between Baseline and 52 Weeks Assessments
NCT00546052 (13) [back to overview]Change in Diastolic Blood Pressure Between Baseline and 52 Week Assessments
NCT00546754 (13) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 6
NCT00546754 (13) [back to overview]Change in Diastolic Blood Pressure From Baseline to Week 12
NCT00546754 (13) [back to overview]Change in Diastolic Blood Pressure From Baseline to Week 6
NCT00546754 (13) [back to overview]Change in Gamma-Glutamyl Transpeptidase (Gamma-GT) From Baseline to Week 12
NCT00546754 (13) [back to overview]Change in Gamma-Glutamyl Transpeptidase (Gamma-GT) From Baseline to Week 6
NCT00546754 (13) [back to overview]Change in Serum Highly Sensitive C-reactive Protein From Baseline to Week 12
NCT00546754 (13) [back to overview]Change in Serum Highly Sensitive C-reactive Protein From Baseline to Week 6
NCT00546754 (13) [back to overview]Change in Systolic Blood Pressure From Baseline to Week 12
NCT00546754 (13) [back to overview]Change in Systolic Blood Pressure From Baseline to Week 6
NCT00546754 (13) [back to overview]Change in Uric Acid From Baseline to Week 12
NCT00546754 (13) [back to overview]Change in Uric Acid From Baseline to Week 6
NCT00546754 (13) [back to overview]Time to Achieve Target Blood Pressure
NCT00546754 (13) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 12
NCT00574834 (1) [back to overview]Changes in Insulin Sensitivity
NCT00605072 (5) [back to overview]Blood Pressure Outcome: Systolic BP
NCT00605072 (5) [back to overview]Cognitive Assessment: Forward Digit Span Test
NCT00605072 (5) [back to overview]Cognitive Assessment: Trail Making Test Part B
NCT00605072 (5) [back to overview]Cognitive Assessment: Hopkins Verbal Learning- Immediate Recall
NCT00605072 (5) [back to overview]Blood Flow Velocity, Sitting
NCT00605202 (1) [back to overview]Plasma Potassium
NCT00621153 (1) [back to overview]Changes in Mean Sitting DBP From Baseline After 4 Weeks of Therapy
NCT00649389 (4) [back to overview]Change in Mean 24-hour Ambulatory Blood Pressure From Baseline to Week 12 or Early Termination
NCT00649389 (4) [back to overview]Percentage of Subjects Who Reached Blood Pressure Goal (<140/90 mmHg; <130/80 mmHg for Subjects With Diabetes, Chronic Renal Disease, or Chronic Cardiovascular Disease)by 12 Weeks
NCT00649389 (4) [back to overview]Change in Seated Systolic Blood Pressure From Baseline to Week 12
NCT00649389 (4) [back to overview]Change From Baseline to Week 12 in Seated Diastolic Blood Pressure (SeDBP).
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Last 6 Hour Ambulatory Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Last 4 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Last 4 Hour Ambulatory Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Last 2 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Last 2 Hour Ambulatory Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Daytime Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Daytime Ambulatory Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean 24-hour Ambulatory Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean 24 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12
NCT00654745 (29) [back to overview]Change in Mean Seated Systolic Blood Pressure (SeSBP) From Week 0 (Baseline) After 3, 6, 9, 12, 15, and 18 Weeks
NCT00654745 (29) [back to overview]Change in Mean Seated Diastolic Blood Pressure (SeDBP) From Week 0 (Baseline) After 3, 6, 9, 12, 15, and 18 Weeks
NCT00654745 (29) [back to overview]Change From Week 0 (Baseline) in Mean ABPM SBP After 12 Weeks of Active Treatment
NCT00654745 (29) [back to overview]Change From Week 0 (Baseline) in Mean ABPM Diastolic Blood Pressure (DBP) After 12 Weeks of Active Treatment
NCT00654745 (29) [back to overview]Change From Week 0 (Baseline) in Mean 24-hour Ambulatory Blood Pressure Monitoring (ABPM) Systolic Blood Pressure (SBP) After 12 Weeks of Active Treatment
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Nighttime Ambulatory Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Nighttime Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 15
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 18
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 3
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 6
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 9
NCT00654745 (29) [back to overview]Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 15
NCT00654745 (29) [back to overview]Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 18
NCT00654745 (29) [back to overview]Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 3
NCT00654745 (29) [back to overview]Number of Participants Achieving Mean Last 6 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12
NCT00654745 (29) [back to overview]Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 6
NCT00654745 (29) [back to overview]Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 9
NCT00661895 (1) [back to overview]Percentage of Subjects Achieving Blood Pressure Goals
NCT00667719 (6) [back to overview]Percentage of Participants Who Achieved a Blood Pressure Response in Mean Sitting Systolic Blood Pressure
NCT00667719 (6) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)
NCT00667719 (6) [back to overview]Number of Participants With Any Adverse Events (AEs), Serious Adverse Events (SAEs) and Death
NCT00667719 (6) [back to overview]Percentage of Participants Achieving the Blood Pressure Control Target of <140/90 mmHg
NCT00667719 (6) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)
NCT00667719 (6) [back to overview]Percentage of Participants Who Achieved a Blood Pressure Response in Mean Sitting Diastolic Blood Pressure
NCT00695955 (6) [back to overview]Change From Baseline in Sitting Clinic Systolic Blood Pressure - Cohort 2
NCT00695955 (6) [back to overview]Change From Baseline in Sitting Clinic Diastolic Blood Pressure - Cohort 1.
NCT00695955 (6) [back to overview]Change From Baseline in Sitting Clinic Diastolic Blood Pressure - Cohort 2.
NCT00695955 (6) [back to overview]Change From Baseline in Sitting Clinic Systolic Blood Pressure - Cohort 1.
NCT00695955 (6) [back to overview]Number of Participants Reporting One or More Treatment-emergent Adverse Events From Day 1 Through End of the Study - Cohort 1.
NCT00695955 (6) [back to overview]Number of Participants Reporting One or More Treatment-emergent Adverse Events From Day 1 Through End of the Study - Cohort 2.
NCT00698646 (6) [back to overview]Change From Baseline to Week 4 in Office Cuff Mean Sitting Systolic Blood Pressure (MSSBP)
NCT00698646 (6) [back to overview]Cumulative Percentage of Patients Achieving the Blood Pressure Control of < 140/90 mmHg
NCT00698646 (6) [back to overview]Cumulative Percentage of Patients Achieving Blood Pressure Goal (MSSBP < 140 mmHg)
NCT00698646 (6) [back to overview]Change From Baseline to Weeks 8, 12 and 16 in Office Cuff Mean Sitting Systolic Blood Pressure (MSSBP)
NCT00698646 (6) [back to overview]Change From Baseline to Week 4, 8, 12 and 16 in Office Cuff Mean Sitting Diastolic Blood Pressure (MSDBP)
NCT00698646 (6) [back to overview]Time in Weeks to Achieving the First Treatment Success (Defined as the Time of the First Achievement of the Target Blood Pressure Goal [MSSBP/MSDBP <140/90 mmHg])
NCT00705575 (4) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to End of Study (Week 12)
NCT00705575 (4) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to Week 8
NCT00705575 (4) [back to overview]Percentage of Patients Achieving the Target Blood Pressure (msSBP < 140 mm Hg and msDBP < 90 mm Hg, and msSBP < 130 mm Hg and msDBP < 80 mm Hg for Diabetics) at Week 8 and Week 12
NCT00705575 (4) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) From Baseline to Week 8 and to Week 12
NCT00739596 (5) [back to overview]Percentage of Responders After 8 Weeks of Treatment.
NCT00739596 (5) [back to overview]Percentage of Participants Achieving BP Control After 8 Weeks of Treatment
NCT00739596 (5) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (MSDBP) After 8 Weeks of Treatment
NCT00739596 (5) [back to overview]Change in Mean Sitting Systolic Blood Pressure (MSSBP) After 8 Weeks of Treatment
NCT00739596 (5) [back to overview]Change in Mean Sitting Pulse Pressure (MSPP) After 8 Weeks of Treatment
NCT00739674 (11) [back to overview]Change in Diastolic Blood Pressure From Baseline to Week 6
NCT00739674 (11) [back to overview]Change in Diastolic Blood Pressure From Baseline to Week 14
NCT00739674 (11) [back to overview]Change in Diastolic Blood Pressure From Baseline to Week 10
NCT00739674 (11) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 6 From Baseline
NCT00739674 (11) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 40 From Baseline
NCT00739674 (11) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 14 From Baseline
NCT00739674 (11) [back to overview]Time to Achieve the Target Blood Pressure From Baseline
NCT00739674 (11) [back to overview]Change in Systolic Blood Pressure From Baseline to Week 6
NCT00739674 (11) [back to overview]Change in Systolic Blood Pressure From Baseline to Week 14
NCT00739674 (11) [back to overview]Change in Systolic Blood Pressure From Baseline to Week 10
NCT00739674 (11) [back to overview]Number of Patients Achieving Target Blood Pressure at Week 10 From Baseline
NCT00760266 (5) [back to overview]Percentage of Subjects Achieving Blood Pressure Control at Weeks 4 and 8
NCT00760266 (5) [back to overview]Percentage of Responders at Week 4 and Week 8
NCT00760266 (5) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) and Mean Sitting Diastolic Blood Pressure (msDBP) (in Patients With msDBP ≥90 mmHg at Baseline) From Baseline to Week 8
NCT00760266 (5) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to Week 4
NCT00760266 (5) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) From Baseline to Week 4
NCT00765674 (4) [back to overview]Change in Mean 24-hour Ambulatory Systolic and Diastolic Blood Pressure From Baseline to End of Study (Week 8)
NCT00765674 (4) [back to overview]Percentage of Patients Achieving Blood Pressure Control at the End of the Study (Week 8)
NCT00765674 (4) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) From Baseline to End of Study (Week 8)
NCT00765674 (4) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to End of Study (Week 8)
NCT00765947 (4) [back to overview]Percentage of Participants (Defined as Estimated Cumulative Control Rate) Reaching Blood Pressure Target in a Stepped Care, Aliskiren-based Regimen
NCT00765947 (4) [back to overview]Changes From Baseline to Week 24 in Mean Sitting Systolic Blood Pressure [msSBP] and Mean Sitting Diastolic Blood Pressure [msDBP]
NCT00765947 (4) [back to overview]Percent of Responders for Mean Sitting Systolic Blood Pressure [msSBP] and for Mean Sitting Diastolic Blood Pressure [msDBP]
NCT00765947 (4) [back to overview]Percentage of Patients (Defined as Estimated Cumulative Control Rate) Reaching Blood Pressure Target in a Stepped-care, Aliskiren-based Regimen by Patient Subgroups of Mild and Moderate Hypertensive Patients, and Non-diabetic and Diabetic Patients.
NCT00772577 (5) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (MSSBP)
NCT00772577 (5) [back to overview]Percentage of Responders (MSSBP < 140 mmHg or ≥ 20 mmHg Decrease From Baseline in MSSBP)
NCT00772577 (5) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (MSDBP)
NCT00772577 (5) [back to overview]Change From Baseline in Mean Sitting Pulse Pressure (MSPP)
NCT00772577 (5) [back to overview]Percentage of Patients Achieving Blood Pressure Control During 8 Weeks
NCT00787605 (6) [back to overview]Percentage of Responders
NCT00787605 (6) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)
NCT00787605 (6) [back to overview]Biomarker Measurements
NCT00787605 (6) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)
NCT00787605 (6) [back to overview]Evaluate the Safety and Tolerability
NCT00787605 (6) [back to overview]Percentage of Patients Achieving Blood Pressure Control
NCT00791258 (59) [back to overview]Percentage of Obese Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on an Angiotensin Converting Enzyme Inhibitor Achieving the Blood Pressure Goals From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on an Angiotensin Converting Enzyme Inhibitor Achieving the Blood Pressure Goals From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Nondihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients With Metabolic Syndrome Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients With Metabolic Syndrome Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients With Metabolic Syndrome Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients With Metabolic Syndrome Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Asain Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Nondihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Diuretic Achieving the Blood Pressure Goals From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Diuretic Achieving the Blood Pressure Goals From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Achieving the Mean 24-hour Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]The Percentage of Subjects Who Achieve BP Goal (<140/90 mmHg for Non-diabetics or <130/80 mmHg for Diabetics) From Baseline to 12 and 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Type 2 Diabetic Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Type 2 Diabetic Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Type 2 Diabetic Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Type 2 Diabetic Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Achieving the Mean 24-hour Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Achieving the Mean Daytime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Achieving the Mean Daytime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Achieving the Mean Nighttime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Achieving the Mean Nighttime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Dihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Obese Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Obese Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Obese Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Asian Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on an Angiotensin II Receptor Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on an Angiotensin II Receptor Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients Achieving Seated Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Beta Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Beta Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Elderly Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Participants Previously on a Dihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Hispanic Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Hispanic Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Hispanic Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Hispanic Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Elderly Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Elderly Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Change in Mean Seated Systolic Blood Pressure From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Elderly Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of Asian Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]The Percentage of Patients Who Achieve Seated Systolic Blood Pressure Goal (<140 mm Hg for Non-diabetics and <130 mm Hg for Diabetics) From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Percentage of Asian Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]The Percentage of Subjects Achieving Seated Diastolic BP Goal (<90 mmHg for Non-diabetics or < 80 mmHg for Subjects With Diabetes) From Baseline to 12 Weeks
NCT00791258 (59) [back to overview]Change From Baseline to Week 12 in Ambulatory Systolic and Diastolic Blood Pressure Values
NCT00791258 (59) [back to overview]Change From Baseline to Week 20 in Ambulatory Systolic and Diastolic Blood Pressure Values
NCT00791258 (59) [back to overview]Change in Mean Seated Diastolic Blood Pressure From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of African American/Black Patients Achieving Seated Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of African American/Black Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of African American/Black Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of African American/Black Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00791258 (59) [back to overview]Percentage of African American/Black Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks
NCT00797316 (5) [back to overview]Change From Baseline to Week 8 in Pulse Pressure
NCT00797316 (5) [back to overview]Percentage of Patients Achieving Blood Pressure Control at Week 8
NCT00797316 (5) [back to overview]Change From Baseline to Week 8 in Mean Sitting Diastolic Blood Pressure (msDBP)
NCT00797316 (5) [back to overview]Change From Baseline to Week 8 in Mean Sitting Systolic Blood Pressure (msSBP)
NCT00797316 (5) [back to overview]Percentage of Participants With Blood Pressure Response at Week 8
NCT00797862 (7) [back to overview]Percentage of Participants Achieving Overall Blood Pressure Control at 8, 16, 24 and 32 Weeks Endpoints
NCT00797862 (7) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP) at Week 24
NCT00797862 (7) [back to overview]Overall Mean Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) Over 8, 16 and 24 Weeks
NCT00797862 (7) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP) at Week 32
NCT00797862 (7) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) at Week 24
NCT00797862 (7) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) at Week 32
NCT00797862 (7) [back to overview]Overall Mean Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP) Over 8, 16, and 24 Weeks
NCT00818883 (15) [back to overview]Percentage of Participants Who Reached Their Trough, Sitting, Clinic Systolic and Diastolic Blood Pressure Targets, Defined as <140/90 mm Hg Without Diabetes or Chronic Kidney Disease or <130/80 mm Hg With Diabetes or Chronic Kidney Disease
NCT00818883 (15) [back to overview]Percentage of Participants Who Reached Their Trough, Sitting, Clinic Systolic Blood Pressure Targets, Defined as <140 mm Hg for Participants Without Diabetes or Chronic Kidney Disease or <130 mm Hg for Participants With Diabetes or Chronic Kidney Disease
NCT00818883 (15) [back to overview]Change From Baseline in the Mean Nighttime (12 AM to 6 AM) Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in 24-hour Mean Diastolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in 24-hour Mean Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in Mean Trough Diastolic Blood Pressure (22 to 24 Hours After Dosing) as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in Mean Trough Systolic Blood Pressure (22 to 24 Hours After Dosing) as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in the Mean Daytime (6 AM to 10 PM) Diastolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in the Mean Daytime (6 AM to 10 PM) Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in the Mean Diastolic Blood Pressure at 0 to 12 Hours After Dosing as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in the Mean Nighttime (12 AM to 6 AM) Diastolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00818883 (15) [back to overview]Change From Baseline in the Mean Systolic Blood Pressure at 0 to 12 Hours After Dosing as Measured by Ambulatory Blood Pressure Monitoring
NCT00818883 (15) [back to overview]Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure
NCT00818883 (15) [back to overview]Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure
NCT00818883 (15) [back to overview]Percentage of Participants Who Reached Their Trough, Sitting, Clinic Diastolic Blood Pressure Target, Defined as <90 mm Hg for Participants Without Diabetes or Chronic Kidney Disease or <80 mm Hg for Participants With Diabetes or Chronic Kidney Disease.
NCT00822107 (1) [back to overview]Chloriuretic Response to a Thiaizde
NCT00834067 (9) [back to overview]Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexipril.
NCT00834067 (9) [back to overview]Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Hydrochlorothiazide.
NCT00834067 (9) [back to overview]AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexiprilat.
NCT00834067 (9) [back to overview]AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexipril.
NCT00834067 (9) [back to overview]AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexipril.
NCT00834067 (9) [back to overview]Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexiprilat.
NCT00834067 (9) [back to overview]AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Hydrochlorothiazide.
NCT00834067 (9) [back to overview]AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexiprilat.
NCT00834067 (9) [back to overview]AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Hydrochlorothiazide.
NCT00835042 (9) [back to overview]AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Hydrochlorothiazide.
NCT00835042 (9) [back to overview]AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexipril.
NCT00835042 (9) [back to overview]AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexiprilat.
NCT00835042 (9) [back to overview]AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexipril.
NCT00835042 (9) [back to overview]Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexipril.
NCT00835042 (9) [back to overview]Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Hydrochlorothiazide.
NCT00835042 (9) [back to overview]AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexiprilat.
NCT00835042 (9) [back to overview]Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexiprilat.
NCT00835042 (9) [back to overview]AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Hydrochlorothiazide.
NCT00846365 (16) [back to overview]Change From Baseline in Nighttime Mean (12am to 6am) Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in Nighttime Mean (12am to 6am) Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring
NCT00846365 (16) [back to overview]Change From Baseline in Trough Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in Trough Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure
NCT00846365 (16) [back to overview]Percentage of Participants Who Achieve a Clinic Diastolic AND Systolic Blood Pressure Response, Defined as <140/90 mm Hg for Participants Without Diabetes or Chronic Kidney Disease (CKD) or <130/80 mm Hg for Participants With Diabetes or CKD
NCT00846365 (16) [back to overview]Percentage of Participants Who Achieve a Clinic Diastolic Blood Pressure Response, Defined as Defined as <90 mm Hg for Participants Without Diabetes or CKD or <80 mm Hg for Participants With Diabetes or CKD
NCT00846365 (16) [back to overview]Percentage of Participants Who Achieve a Clinic Systolic Blood Pressure Response, Defined as <140 mm Hg for Participants Without Diabetes or CKD or <130 mm Hg for Participants With Diabetes or CKD
NCT00846365 (16) [back to overview]Change From Baseline in 12-hr Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline to Week 4 in Trough, Sitting, Clinic Systolic Blood Pressure.
NCT00846365 (16) [back to overview]Change From Baseline to Week 8 in Trough, Sitting, Clinic Systolic Blood Pressure.
NCT00846365 (16) [back to overview]Change From Baseline in 12-hr Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in 24-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in 24-hour Mean Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in Daytime Mean (6am to 10pm) Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00846365 (16) [back to overview]Change From Baseline in Daytime Mean (6am to 10pm) Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.
NCT00865124 (4) [back to overview]Mitral Annulus Velocities on Tissue Doppler (Delta E/e' Ratio), a Measure of Diastolic Function (With Angiotensin II)
NCT00865124 (4) [back to overview]Change in Renal Plasma Flow
NCT00865124 (4) [back to overview]Change in Mitral Annulus Velocities on Tissue Doppler (Delta E/e' Ratio), a Measure of Diastolic Function
NCT00865124 (4) [back to overview]Change in Coronary Flow Reserve From Baseline to 6 Months
NCT00867490 (12) [back to overview]Change in Sitting Pulse Rate During the Core Phase of the Study
NCT00867490 (12) [back to overview]Change in Sitting Pulse Rate During the Extension Phase of the Study
NCT00867490 (12) [back to overview]Percentage of Patients Who Achieved Normalized Blood Pressure During the Core Phase of the Study
NCT00867490 (12) [back to overview]Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Core Phase of the Study
NCT00867490 (12) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Extension Phase of the Study
NCT00867490 (12) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Core Phase of the Study
NCT00867490 (12) [back to overview]Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Extension Phase of the Study
NCT00867490 (12) [back to overview]Change in Sitting Pulse Pressure During the Core Phase of the Study
NCT00867490 (12) [back to overview]Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Core Phase of the Study
NCT00867490 (12) [back to overview]Change in Sitting Pulse Pressure During the Extension Phase of the Study
NCT00867490 (12) [back to overview]Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Core Phase of the Study
NCT00867490 (12) [back to overview]Percentage of Patients Who Achieved Normalized Blood Pressure During the Core Phase of the Study
NCT00871871 (7) [back to overview]Part I: Change in the Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady State in Participants With Impaired Glucose Tolerant (IGT)
NCT00871871 (7) [back to overview]Part I: Change in Insulin Secretion at Steady-state Compared to Placebo in Participants Who Had Normal Glucose Tolerance (NGT)
NCT00871871 (7) [back to overview]Part I: Change in Insulin Secretion at Steady-state Compared to Placebo in Participants With Impaired Fasting Glucose (IFG)
NCT00871871 (7) [back to overview]Part I: Change in Insulin Secretion at Steady-state Compared to Placebo in Participants With Impaired Glucose Tolerance (IGT)
NCT00871871 (7) [back to overview]Part I: Change in the Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady State in Participants With Impaired Fasting Glucose (IFG)
NCT00871871 (7) [back to overview]Part I: Change in the Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady State in Participants With Normal Glucose Tolerant (NGT)
NCT00871871 (7) [back to overview]Part II: Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady-state
NCT00886600 (5) [back to overview]Mean Change From Baseline in Sitting Diastolic Blood Pressure (siDBP) After Adding HCTZ 24 Hours After Morning Dose at Week 6
NCT00886600 (5) [back to overview]Mean Change From Week 4 in Sitting Diastolic Blood Pressure (siDBP) Adding HCTZ 24 Hours After Morning Dose at Week 6
NCT00886600 (5) [back to overview]Mean Change From Baseline in 24-hour Systolic Ambulatory Blood Pressure Monitoring (ABPM) at Week 4
NCT00886600 (5) [back to overview]Mean Change From Baseline in 24-hour Diastolic Ambulatory Blood Pressure Monitoring (ABPM) at Week 4
NCT00886600 (5) [back to overview]Mean Change From Baseline in Sitting Diastolic Blood Pressure (siDBP) 24 Hours After Morning Dose at Week 4
NCT00887510 (2) [back to overview]Change in Total Adiponectin Level After Addition of Trandolapril to HCTZ Compared With Change in Adiponectin After Addition of HCTZ to Trandolapril
NCT00887510 (2) [back to overview]Change in Oral Glucose Tolerance Test (OGTT) Area Under Curve (AUC) After Addition of Trandolapril to Hydrochlorothiazide (HCTZ) Compared With Change in OGTT AUC After Addition of HCTZ to Trandolapril
NCT00890084 (8) [back to overview]Percentage of Prescribers Who Adhered to European Society of Hypertension/European Society of Cardiology (ESH/ESC) Guidelines 2007
NCT00890084 (8) [back to overview]Percentage of Patients With Blood Pressure < 140/90 mm Hg
NCT00890084 (8) [back to overview]Percentage of Patients With Blood Pressure < 130/80 mm Hg
NCT00890084 (8) [back to overview]Percentage of Patients in Whom the Prescriber Decide to Further Lower the Blood Pressure to < 130/80 mm Hg
NCT00890084 (8) [back to overview]Change in Concomitant Antihypertensive Drugs Given at Study Entry
NCT00890084 (8) [back to overview]BP Response Rate (Drop of Systolic BP of 10mmHg or More)
NCT00890084 (8) [back to overview]Absolute Blood Pressure Decrease
NCT00890084 (8) [back to overview]Treatment Patterns
NCT00890591 (4) [back to overview]Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 in Third Titrated Group (Olmesartan + Hydrochorothiazide + Amlodipine)
NCT00890591 (4) [back to overview]Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 in Second Titrated Group (Olmesartan 40 mg + 25 mg Hydrochlorothiazide)
NCT00890591 (4) [back to overview]Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 (Olmesartan 20 mg Monotherapy)
NCT00890591 (4) [back to overview]Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 in First Titrated Group (Olmesartan 20 mg + 12.5 mg Hydrochlorothiazide)
NCT00896389 (10) [back to overview]Change in Plasma Sodium/Potassium Level Due to Salt-loading
NCT00896389 (10) [back to overview]Change in Plasma Renin Activity Due to Salt-loading
NCT00896389 (10) [back to overview]Change in Plasma Aldosterone Level Due to Salt-loading
NCT00896389 (10) [back to overview]Blood Pressure Change During Salt Loading
NCT00896389 (10) [back to overview]Blood Pressure Change After 7 Days of Low Dose (12.5 mg) of HCTZ
NCT00896389 (10) [back to overview]Blood Pressure Change After 7 Days of High Dose (25 mg) of HCTZ
NCT00896389 (10) [back to overview]Change in Plasma Sodium/Potassium Level During Low Dose of HCTZ
NCT00896389 (10) [back to overview]Change in Plasma Sodium/Potassium Level During High Dose of HCTZ
NCT00896389 (10) [back to overview]Fasting Glucose Change After 7 Days of High Dose (25mg) of HCTZ
NCT00896389 (10) [back to overview]Fasting Glucose Change After 7 Days of Low Dose (12.5 mg) of HCTZ
NCT00902304 (12) [back to overview]Change in Absolute Cardiovascular Risk Score
NCT00902304 (12) [back to overview]Number of Patients With Major Clinical Endpoints
NCT00902304 (12) [back to overview]Participants With End Organ Disease at Baseline and Week 26
NCT00902304 (12) [back to overview]Number of Patients With at Least One Adverse Events Attributable to Anti-hypertensive Therapy
NCT00902304 (12) [back to overview]Percentage of Patients Who Have Achieved Their Pre-specified (Individualized National Heart Foundation of Australia Criteria) Blood Pressure (BP) Target
NCT00902304 (12) [back to overview]Change in Self-care Behavior Score From Baseline to Week 26
NCT00902304 (12) [back to overview]Number of 'Early Responder' Patients Who Achieve Individualized Blood Pressure Control After 1 or 2 Adjustments
NCT00902304 (12) [back to overview]Number of Patients With Depression
NCT00902304 (12) [back to overview]Change in the EQ-5D Score
NCT00902304 (12) [back to overview]Change in Mean Sitting Systolic Blood Pressure
NCT00902304 (12) [back to overview]Change in Mean Sitting Diastolic Blood Pressure
NCT00902304 (12) [back to overview]Change in Center for Epidemiologic Studies Depression (CES-D) Score From Baseline to Week 26
NCT00902538 (10) [back to overview]Change in 24-hour Systolic Blood Pressure Assessed by 24-hour Ambulatory Blood Pressure Measurement.
NCT00902538 (10) [back to overview]Change in Seated Diastolic Blood Pressure (SeDBP) of the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg vs. OM/AML 40/10 mg
NCT00902538 (10) [back to overview]Change in Seated Systolic Blood Pressure (SeSBP) of the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg vs. OM/AML 40/10 mg
NCT00902538 (10) [back to overview]Change in 24-hour Diastolic Blood Pressure (DBP) Assessed by 24-hour Ambulatory Blood Pressure Measurement (ABPM).
NCT00902538 (10) [back to overview]Number of Subjects Achieving Blood Pressure (BP) Goal at Week 16.
NCT00902538 (10) [back to overview]In Non-responders, the Number of Subject Meeting Their Blood Pressure Goals Associated With the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg.
NCT00902538 (10) [back to overview]In Non-responders, the Change in Seated Diastolic Blood Pressure Associated With the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg.
NCT00902538 (10) [back to overview]In Non-responders, the Change in Seated Systolic Blood Pressure Associated With the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg.
NCT00902538 (10) [back to overview]In Non-responders, the Change in 24-hour Systolic Blood Pressure Assessed by 24-hour Ambulatory Blood Pressure Measurement.
NCT00902538 (10) [back to overview]In Non-responders, the Change in 24-hour Diastolic Blood Pressure Assessed by 24-hour Ambulatory Blood Pressure Measurement.
NCT00904215 (4) [back to overview]Change in WHO-QOL (WHO-Quality Of Life)
NCT00904215 (4) [back to overview]Change in VAS (Visual Analog Scale)
NCT00904215 (4) [back to overview]Change in SBP (Systolic Blood Pressure)
NCT00904215 (4) [back to overview]Change in DBP (Diastolic Blood Pressure)
NCT00923091 (10) [back to overview]Change in Seated Diastolic Blood Pressure (SeDBP).
NCT00923091 (10) [back to overview]Number of Subjects Reaching Blood Pressure Goal From Week 18 to Week 22
NCT00923091 (10) [back to overview]Number of Subjects Reaching Blood Pressure Goal at Week 26
NCT00923091 (10) [back to overview]Number of Subjects Reaching Blood Pressure Goal at Week 10
NCT00923091 (10) [back to overview]Change in Seated Systolic Blood Pressure From Week 18 to Week 22
NCT00923091 (10) [back to overview]Change in Seated Systolic Blood Pressure (SeDBP).
NCT00923091 (10) [back to overview]Change in Seated Systolic Blood Pressure (SeDBP) During Open-Label Period VI (Titration Effect From OM/AML/HCTZ 40/5/25 to 40/10/25.
NCT00923091 (10) [back to overview]Change in Seated Diastolic Blood Pressure From Week 22 to Week 26
NCT00923091 (10) [back to overview]Change in Seated Diastolic Blood Pressure From Week 18 to Week 22
NCT00923091 (10) [back to overview]Change in Seated Systolic Blood Pressure From Week 22 to Week 26
NCT00926289 (15) [back to overview]Number of Patients With DBP Control (DBP < 90 mmHg) at Week 5
NCT00926289 (15) [back to overview]Number of Patients With DBP Control (DBP < 90 mmHg) at Week 7
NCT00926289 (15) [back to overview]Number of Patients With SBP Control (SBP < 140 mmHg) at Week 3
NCT00926289 (15) [back to overview]Number of Patients With SBP Control (SBP < 140 mmHg) at Week 5
NCT00926289 (15) [back to overview]Number of Patients With SBP Control (SBP < 140 mmHg) at Week 7
NCT00926289 (15) [back to overview]Number of Patients With Systolic Blood Pressure (SBP) Response at Week 7
NCT00926289 (15) [back to overview]BP Categories at Week 7
NCT00926289 (15) [back to overview]Change From Baseline in Mean Seated Trough Cuff Diastolic Blood Pressure (DBP) to Week 7
NCT00926289 (15) [back to overview]Change From Baseline in Mean Seated Trough Cuff SBP to Week 3
NCT00926289 (15) [back to overview]Change From Baseline in Mean Seated Trough Cuff SBP to Week 5
NCT00926289 (15) [back to overview]Change From Baseline in Mean Seated Trough Cuff Systolic Blood Pressure (SBP) to Week 7
NCT00926289 (15) [back to overview]Number of Participants With DBP Response at Week 7
NCT00926289 (15) [back to overview]Number of Patients With Blood Pressure (BP) Control at Week 7
NCT00926289 (15) [back to overview]Number of Patients With BP Control at Week 7
NCT00926289 (15) [back to overview]Number of Patients With DBP Control (DBP < 90 mmHg) at Week 3
NCT00931710 (6) [back to overview]Change in Mean Sitting Systolic and Diastolic Blood Pressure After 12 Weeks
NCT00931710 (6) [back to overview]Change in Mean Sitting Diastolic Blood Pressure After 6 Weeks
NCT00931710 (6) [back to overview]Cumulative Percentage of Patients Achieving Blood Pressure Control
NCT00931710 (6) [back to overview]Cumulative Percentage of Patients With Incidence of Peripheral Edema Before or at the Corresponding Visit
NCT00931710 (6) [back to overview]Cumulative Percentage of Treatment Responders
NCT00931710 (6) [back to overview]Change in Mean Sitting Systolic Blood Pressure After 6 Weeks
NCT00942994 (6) [back to overview]Percentage of Responders (Defined as Patients With MSSBP < 140 mmHg or a Reduction From Baseline in MSSBP of ≥20 mmHg) During 8 Weeks.
NCT00942994 (6) [back to overview]Percentage of Patients Achieving Blood Pressure Control (Defined as MSSBP < 140 mmHg and MSDBP < 90 mmHg) During 8 Weeks
NCT00942994 (6) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (MSSBP) at Week 8
NCT00942994 (6) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (MSSBP) at Week 2 and Week 4
NCT00942994 (6) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (MSDBP) at Week 8
NCT00942994 (6) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (MSDBP) at Week 2 and Week 4
NCT00953680 (4) [back to overview]Area Under the Curve (AUC(0 to Infinity)) of HCTZ
NCT00953680 (4) [back to overview]Area Under the Curve (AUC(0 to Infinity)) of Losartan
NCT00953680 (4) [back to overview]Peak Plasma Concentration (Cmax) of HCTZ Following Single Dose Administration of Losartan/HCTZ or Losartan and HCTZ
NCT00953680 (4) [back to overview]Peak Plasma Concentration (Cmax) for Losartan
NCT00976495 (4) [back to overview]Adjusted Mean Change From Baseline in Daytime (0900 to 2100 Hours) Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])
NCT00976495 (4) [back to overview]Adjusted Percent Change From Baseline in Glomerular Filtration Rate (GFR) at Week 12 (Modified Last Observation Carried Forward [MLOCF])
NCT00976495 (4) [back to overview]Adjusted Mean Change From Baseline in Nighttime (0100 to 0600 Hours) Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])
NCT00976495 (4) [back to overview]Adjusted Mean Change From Baseline in 24-Hour Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])
NCT00996281 (2) [back to overview]Percentage of Participants With at Least 1 Adverse Event
NCT00996281 (2) [back to overview]Percentage of Participants With Serum Creatinine Elevations Greater Than 50% From Baseline and Greater Than the Upper Limit of Normal (ULN)
NCT01030458 (4) [back to overview]Proportion of Patients Reaching Blood Pressure Control at the End of Follow-up
NCT01030458 (4) [back to overview]Side-effects to Study Medications
NCT01030458 (4) [back to overview]Sitting Systolic Blood Pressure on Automated Measurement
NCT01030458 (4) [back to overview]Time to Blood Pressure Control
NCT01033071 (18) [back to overview]Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.
NCT01033071 (18) [back to overview]Change From Baseline in the Mean Diastolic Blood Pressure During Each Hour of the 24-hour Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in the Mean Systolic Blood Pressure During Each Hour of the 24-hour Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure.
NCT01033071 (18) [back to overview]Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.
NCT01033071 (18) [back to overview]Percent of Participants Who Reached Target Clinic Systolic Blood Pressure of <140 mm Hg and/or Reduction of ≥20 mm Hg From Baseline and Target Clinic Diastolic Blood Pressure of <90 mm Hg and/or Reduction of ≥10 mm Hg From Baseline.
NCT01033071 (18) [back to overview]Percentage of Participants Who Reached Target Clinic Diastolic Blood Pressure of <90 mm Hg and/or Reduction of ≥10 mm Hg From Baseline.
NCT01033071 (18) [back to overview]Percentage of Participants Who Reached Target Clinic Systolic Blood Pressure of <140 mm Hg and/or Reduction of ≥20 mm Hg From Baseline.
NCT01033071 (18) [back to overview]Change From Baseline in 24-hour Mean Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in 24-hour Mean Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Mean Daytime (6 AM to 10 PM) Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Mean Daytime (6 AM to 10 PM) Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Mean Nighttime (12 AM to 6 AM) Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Mean Nighttime (12 AM to 6 AM) Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Mean Trough Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in Mean Trough Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in the Mean Diastolic Blood Pressure at 0 to 12 Hours After Dosing by Ambulatory Blood Pressure Monitoring.
NCT01033071 (18) [back to overview]Change From Baseline in the Mean Systolic Blood Pressure at 0 to 12 Hours After Dosing by Ambulatory Blood Pressure Monitoring.
NCT01050062 (5) [back to overview]Systolic Blood Pressure (SBP)
NCT01050062 (5) [back to overview]Incidence of Adverse Events (AEs)
NCT01050062 (5) [back to overview]Blood Pressure Normalised Rate
NCT01050062 (5) [back to overview]Target Blood Pressure Achievement Rate
NCT01050062 (5) [back to overview]Diastolic Blood Pressure (DBP)
NCT01096667 (26) [back to overview]Change From Baseline on Daytime Average Heart Rate at Week 4
NCT01096667 (26) [back to overview]Baseline Seated, Triplicate Trough Heart Rate
NCT01096667 (26) [back to overview]Change From Baseline on 24-hour Average SBP at Week 4
NCT01096667 (26) [back to overview]Change From Baseline on Nighttime Average DBP at Week 4
NCT01096667 (26) [back to overview]Change From Baseline on Nighttime Average Heart Rate at Week 4
NCT01096667 (26) [back to overview]Change From Baseline on Nighttime Average SBP at Week 4
NCT01096667 (26) [back to overview]Number of Participants Who Discontinued Study Drug Due to an AE
NCT01096667 (26) [back to overview]Change From Baseline on 24-hour Urinary Glucose Excretion at Week 4
NCT01096667 (26) [back to overview]Number of Participants Who Experienced an Adverse Event (AE)
NCT01096667 (26) [back to overview]Baseline 24-hour, Daytime and Nightime Average Diastolic Blood Pressure (DBP)
NCT01096667 (26) [back to overview]Baseline 24-hour, Daytime and Nightime Average Heart Rate
NCT01096667 (26) [back to overview]Baseline Average Daytime and Nighttime SBP
NCT01096667 (26) [back to overview]Baseline Seated, Triplicate Trough DBP
NCT01096667 (26) [back to overview]Baseline Fasting Plasma Glucose (FPG)
NCT01096667 (26) [back to overview]Baseline 24-hour Average Urinary Glucose Excretion
NCT01096667 (26) [back to overview]Change From Baseline in Seated, Triplicate Trough SBP at Week 4
NCT01096667 (26) [back to overview]Baseline 24-hour Average Systolic Blood Pressure (SBP)
NCT01096667 (26) [back to overview]Change From Baseline on 24-hour Average DBP at Week 4
NCT01096667 (26) [back to overview]Change From Baseline on 24-hour Average Heart Rate at Week 4
NCT01096667 (26) [back to overview]Change From Baseline in Seated, Triplicate Trough Heart Rate at Week 4
NCT01096667 (26) [back to overview]Change From Baseline in Seated, Triplicate Trough DBP at Week 4
NCT01096667 (26) [back to overview]Change From Baseline in FPG at Week 4
NCT01096667 (26) [back to overview]Change From Baseline in FPG at Week 2
NCT01096667 (26) [back to overview]Baseline Seated, Triplicate Trough SBP
NCT01096667 (26) [back to overview]Change From Baseline on Daytime Average DBP at Week 4
NCT01096667 (26) [back to overview]Change From Baseline on Daytime Average SBP at Week 4
NCT01103245 (8) [back to overview]Plasma Insulin
NCT01103245 (8) [back to overview]Plasma Insulin
NCT01103245 (8) [back to overview]Plasma Glucose
NCT01103245 (8) [back to overview]Plasma Insulin
NCT01103245 (8) [back to overview]Plasma Glucose
NCT01103245 (8) [back to overview]Plasma Insulin
NCT01103245 (8) [back to overview]Plasma Glucose
NCT01103245 (8) [back to overview]Plasma Glucose
NCT01149473 (6) [back to overview]AUC0-t of Losartan(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)
NCT01149473 (6) [back to overview]Cmax of Losartan(Maximum Observed Concentration of Drug Substance in Plasma)
NCT01149473 (6) [back to overview]AUC0-inf of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Infinity)
NCT01149473 (6) [back to overview]AUC0-inf of Losartan(Area Under the Concentration-time Curve From Time Zero to Infinity)
NCT01149473 (6) [back to overview]AUC0-t of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)
NCT01149473 (6) [back to overview]Cmax of Hydrochlorothiazide(Maximum Observed Concentration of Drug Substance in Plasma)
NCT01149486 (9) [back to overview]AUC0-t of Losartan(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)
NCT01149486 (9) [back to overview]Cmax of Hydroclorothiazide(Maximum Observed Concentration of Drug Substance in Plasma)
NCT01149486 (9) [back to overview]Cmax of Losartan Carboxy Acid(Maximum Observed Concentration of Drug Substance in Plasma)
NCT01149486 (9) [back to overview]Cmax of Losartan(Maximum Observed Concentration of Drug Substance in Plasma)
NCT01149486 (9) [back to overview]AUC0-inf of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Infinity)
NCT01149486 (9) [back to overview]AUC0-inf of Losartan(Area Under the Concentration-time Curve From Time Zero to Infinity)
NCT01149486 (9) [back to overview]AUC0-t of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)
NCT01149486 (9) [back to overview]AUC0-t of Losartan Carboxy Acid(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)
NCT01149486 (9) [back to overview]AUC0-inf of Losartan Carboxy Acid(Area Under the Concentration-time Curve From Time Zero to Infinity)
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, Left Atrial Volume (Biplane Simpson's Method) in Combination of Aliskiren With Amlodipine
NCT01176032 (20) [back to overview]Change From Baseline in Reduction of Left Ventricular Mass Index (LVMI)
NCT01176032 (20) [back to overview]Change From Baseline of LVMI in Combination of Aliskiren With Amlodipine
NCT01176032 (20) [back to overview]Change From Baseline in Biomarkers in Heart Disease
NCT01176032 (20) [back to overview]Change From Baseline in Combination of Aliskiren With Amlodipine in Biomarkers of Heart Disease.
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, LV Ejection Fraction (Teicholz), and LV Ejection Fraction (Simpson)
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, LV End-diastolic Volume by Simpson's Rule, and LV End-systolic Volume by Simpson's Rule
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, LV End-diastolic Volume by Simpson's Rule, and LV End-systolic Volume by Simpson's Rule in Combination of Aliskiren With Amlodipine
NCT01176032 (20) [back to overview]Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Patients With Satisfactory Response Rate
NCT01176032 (20) [back to overview]Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Patients With SBP < 140 mmHg and DBP < 90 mmHg Compared to Baseline
NCT01176032 (20) [back to overview]Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Rate of Use of Added Antihypertensive Rescue Drugs
NCT01176032 (20) [back to overview]Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Reduction in Diastolic Blood Pressure (DBP)
NCT01176032 (20) [back to overview]Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Reduction in Systolic Blood Pressure (SBP)
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, LV Ejection Fraction (Teicholz), and LV Ejection Fraction (Simpson) in Combination of Aliskiren With Amlodipine
NCT01176032 (20) [back to overview]Change From Baseline in Biomarker Such as Aldosterone (Aldo) in Heart Disease
NCT01176032 (20) [back to overview]Change From Baseline in Biomarker Such as Aldosterone (Aldo) in Heart Disease in Combination of Aliskiren With Amlodipine
NCT01176032 (20) [back to overview]Change From Baseline in C-terminal Propeptide of Procollagen Type I (PICP)
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, LA (Left Atrium) Diameter
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, LA (Left Atrium) Diameter in Combination of Aliskiren With Amlodipine
NCT01176032 (20) [back to overview]Change From Baseline in Left Ventricular (LV) Function, Left Atrial Volume (Biplane Simpson's Method)
NCT01256411 (5) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) and Mean Sitting Diastolic Blood Pressure (msDBP) (Analysis by Maximum Treatment)
NCT01256411 (5) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) and Mean Sitting Diastolic Blood Pressure (msDBP) (Analysis by Mono or Combination Therapy)
NCT01256411 (5) [back to overview]Number of Participants With Blood Pressure Control Rate of <140/90 mmHg (Analysis by Maximum Treatment)
NCT01256411 (5) [back to overview]Number of Participants With Blood Pressure Control Rate of <140/90 mmHg (Analysis by Mono or Combination Therapy)
NCT01256411 (5) [back to overview]Number of Participants With Adverse Events, Serious Adverse Events, and Deaths (Analysis by Actual Treatment)
NCT01259297 (8) [back to overview]Number of Participants With Renal Dysfunction in Aliskiren Based Regimen Versus Non-Aliskiren Based Regimen
NCT01259297 (8) [back to overview]Percentage of Participants With Standard Assessment of Global Activities in the Elderly (SAGE) Dimensions (Part II)
NCT01259297 (8) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)
NCT01259297 (8) [back to overview]Change From Baseline to End of Study in Standard Assessment of Global Activities in the Elderly (SAGE) Dimensions (Part I)
NCT01259297 (8) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)
NCT01259297 (8) [back to overview]Number of Participants With Total Mortality in Aliskiren Based Regimen Versus Non-aliskiren Based Regimen
NCT01259297 (8) [back to overview]Number of Participants With Composite Cardiovascular Endpoints in Aliskiren+Amlodipine/HCTZ Group Versus All Placebo Group
NCT01259297 (8) [back to overview]Number of Participants With Composite Cardiovascular Endpoints in Aliskiren Based Regimen Versus Non-Aliskiren Based Regimen
NCT01276288 (27) [back to overview]Maximum Measured Concentration of Empa in Plasma (Cmax, ss)
NCT01276288 (27) [back to overview]Change in Urine pH From Baseline
NCT01276288 (27) [back to overview]Maximum Measured Concentration of TOR in Plasma (Cmax, ss)
NCT01276288 (27) [back to overview]The Change in Micturition Frequency From the Baseline
NCT01276288 (27) [back to overview]Number of Subjects With Clinical Relevant Abnormalities in Vital Signs, Clinical Laboratory Tests, 12-lead Resting Electrocardiogram (ECG), Physical Examination and Assessment of Tolerability by the Investigator
NCT01276288 (27) [back to overview]Changes in Bicarbonate Concentrations of Calcium, Bicarbonate Ions and Base Excess in Capillary or Arterialised Blood From Baseline
NCT01276288 (27) [back to overview]Change in Urinary Excretion in a 24-hour Period of Sodium, Potassium, Magnesium, Chloride, Calcium, Phosphate, Creatinine, Uric Acid, Glucose From Baseline
NCT01276288 (27) [back to overview]Change in Serum Concentration of Sodium, Potassium, Magnesium, Calcium, Chloride, Phosphate, Glucose and Urea From Baseline
NCT01276288 (27) [back to overview]The Change in Total Muscle Sympathetic Nerve Activity (MSNA) From Off- Treatment
NCT01276288 (27) [back to overview]Change in Clearance of Sodium, Potassium, Creatinine, Magnesium, Chloride,Calcium, Phosphate and Uric Acid From Baseline
NCT01276288 (27) [back to overview]Change in pH in Capillary or Arterialised Blood From Baseline
NCT01276288 (27) [back to overview]Maximum Measured Concentration of HCT in Plasma (Cmax, ss)
NCT01276288 (27) [back to overview]Urinary Sodium Excretion Over 24-hour run-in Periods
NCT01276288 (27) [back to overview]Change in Urinary Excretion in a 24-hour Period of N-terminal Telopeptide (NTx) From Baseline
NCT01276288 (27) [back to overview]Change in Urinary Weight From Baseline
NCT01276288 (27) [back to overview]Change in Urine Osmolality From Baseline
NCT01276288 (27) [back to overview]Change in Serum Concentration of Renin, Intact Parathyroid Hormone (iPTH) and 1,25-dihydroxyvitamin D From Baseline
NCT01276288 (27) [back to overview]Change in Serum Concentration of Creatinine and Uric Acid From Baseline
NCT01276288 (27) [back to overview]Change in Urea Concentration in Urine
NCT01276288 (27) [back to overview]Change in Serum Osmolality From Baseline
NCT01276288 (27) [back to overview]Change in Serum Concentration of Fibroblast Growth Factor-23 (FGF- 23) From Baseline
NCT01276288 (27) [back to overview]Change in Serum Concentration of Alkaline Phosphatase (ALP) From Baseline
NCT01276288 (27) [back to overview]Change in Serum Concentration of Aldosterone From Baseline
NCT01276288 (27) [back to overview]Change in Body Weight From Baseline
NCT01276288 (27) [back to overview]Area Under the Concentration-time Curve of TOR in Plasma (AUCτ,ss)
NCT01276288 (27) [back to overview]Area Under the Concentration-time Curve of HCT in Plasma (AUCτ,ss)
NCT01276288 (27) [back to overview]Area Under the Concentration-time Curve of Empa in Plasma (AUCτ,ss)
NCT01302691 (7) [back to overview]Percentage of Participants Who Experience ≥1 Drug-related AE
NCT01302691 (7) [back to overview]Percentage of Participants Who Experience ≥1 Drug-related SAE
NCT01302691 (7) [back to overview]Percentage of Participants Who Experience ≥1 Adverse Event (AE)
NCT01302691 (7) [back to overview]Change in Mean Trough Sitting Diastolic Blood Pressure (SiDBP)
NCT01302691 (7) [back to overview]Percentage of Participants Who Had Study Drug Stopped Due to an AE
NCT01302691 (7) [back to overview]Percentage of Participants Who Experience ≥1 Serious Adverse Event (SAE)
NCT01302691 (7) [back to overview]Change in Mean Trough Sitting Systolic Blood Pressure (SiSBP)
NCT01302899 (1) [back to overview]Number of Participants With Adverse Events, Serious Adverse Events and Death as Assessment of Safety and Tolerability of Aliskiren Added to Ramipril
NCT01309828 (4) [back to overview]Percentage of Participants at Final Visit Who Achieved Both a Clinic Systolic and Diastolic Blood Pressure Response
NCT01309828 (4) [back to overview]Percentage of Participants at Final Visit Who Achieve Target Systolic Blood Pressure <130 mm Hg
NCT01309828 (4) [back to overview]Number of Participants With at Least 1 Adverse Event (AE)
NCT01309828 (4) [back to overview]Percentage of Participants at Final Visit Who Achieved Target Diastolic Blood Pressure <80 mm Hg
NCT01365481 (5) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (MsDBP) at End Point (Week 78 or Last Observation Carried Forward (LOCF)
NCT01365481 (5) [back to overview]Number of Participants With MSSBP, MSDBP and (MSSBP and MSDBP Combined) < 95th Percentile for Gender, Age, and Height
NCT01365481 (5) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) at End Point (Week 78 or Last Observation Carried Forward (LOCF)
NCT01365481 (5) [back to overview]Percentage of Chronic Kidney Disease (CKD) Patients Who Had Estimated Glomerular Filtration Rate (eGFR) Decrease > 25 % From Baselinefrom Baseline to End Point
NCT01365481 (5) [back to overview]Percentage of Chronic Kidney Disease (CKD) Patients Who Had >=50% Reduction in Urine Albumin/Creatinine Ratio (UACR) From Baseline to End Point
NCT01370655 (7) [back to overview]Change From Baseline in Urine Potassium at 24 Hours Post-dose on Day 28
NCT01370655 (7) [back to overview]Change From Baseline in Time-weighted Average Over 24 Hours Post Dose (TWA [0-24]) in Systolic Blood Pressure (SBP)
NCT01370655 (7) [back to overview]Change From Baseline in Time-weighted Average Over 24 Hours Post Dose (TWA [0-24]) in Diastolic Blood Pressure (DBP)
NCT01370655 (7) [back to overview]Change From Baseline in Urine Sodium at 24 Hours Post-dose on Day 1
NCT01370655 (7) [back to overview]Percentage of Participants Who Had Study Discontinued During the Study Due to an Adverse Event (AE)
NCT01370655 (7) [back to overview]Percentage of Participants Who Experienced at Least 1 Drug-related Adverse Event (AE)
NCT01370655 (7) [back to overview]Percentage of Participants Who Experienced at Least 1 Adverse Event (AE)
NCT01519635 (1) [back to overview]Renal Oxygenation Changes After Chronic Treatment With Aliskiren or Hydrochlorothiazide
NCT01658657 (1) [back to overview]Blood Pressure Control, as Defined as Office BP Measurement of <140 mmHg Systolic and <90 mmHg Diastolic
NCT01692301 (11) [back to overview]Change From Baseline in Mean 24-hour Ambulatory Pulse Pressure (maPP)
NCT01692301 (11) [back to overview]Change From Baseline in Mean 24-hour Systolic Blood Pressure (maSBP)
NCT01692301 (11) [back to overview]Change From Baseline in Mean Arterial Pressure (MAP)
NCT01692301 (11) [back to overview]Change From Baseline in Mean Central Pulse (CPP) Pressure
NCT01692301 (11) [back to overview]Change From Baseline in Mean Pulse Wave Velocity (PWV)
NCT01692301 (11) [back to overview]Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)
NCT01692301 (11) [back to overview]Change From Baseline in Mean 24-hour Diastolic Blood Pressure (maDBP)
NCT01692301 (11) [back to overview]Change From Baseline in Mean Central Aortic Systolic Pressure (CASP) at 12 Weeks
NCT01692301 (11) [back to overview]Change From Baseline in Mean Central Aortic Systolic Pressure (CASP) at 52 Weeks
NCT01692301 (11) [back to overview]Change From Baseline in Mean Sitting Pulse Pressure (msPP)
NCT01692301 (11) [back to overview]Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)
NCT01911780 (6) [back to overview]Change From Baseline in Mean Seated DBP at Trough After 8 Weeks of the Double-blind Period.
NCT01911780 (6) [back to overview]Change From Baseline in Mean Seated SBP at Trough After 8 Weeks of the Double-blind Period.
NCT01911780 (6) [back to overview]The Percentage of Patients With DBP<90 mmHg and SBP<140 mmHg Blood Pressure at Trough After 8 Weeks of Double-blind Period.
NCT01911780 (6) [back to overview]Change From Baseline in Mean DBP Pressure at Trough After 52 Weeks of the Extension Period.
NCT01911780 (6) [back to overview]Change From Baseline in Mean Seated SBP at Trough After 52 Weeks of the Extension Period.
NCT01911780 (6) [back to overview]The Number of Patients With DBP<90 mmHg and SBP<140 mmHg Blood Pressure at Trough After 52 Weeks of Extension Period.
NCT01975246 (3) [back to overview]Change From Baseline in Mean Seated DBP at Trough After 8 Weeks of the Double-blind Period.
NCT01975246 (3) [back to overview]Change From Baseline in Mean Seated SBP at Trough After 8 Weeks of the Double-blind Period.
NCT01975246 (3) [back to overview]The Proportion of Patients With DBP<90 mmHg and SBP<140 mmHg as Seated Blood Pressure at Trough After 8 Weeks of the Double-blind Period
NCT01983462 (2) [back to overview]Aortic Stiffness
NCT01983462 (2) [back to overview]24 Hour Average Systolic Blood Pressure
NCT02016183 (4) [back to overview]Changes From Baseline in Systolic Blood Pressure (SBP) at Each Time Point
NCT02016183 (4) [back to overview]Changes From Baseline in Diastolic Blood Pressure (DBP) at Each Time Point
NCT02016183 (4) [back to overview]Number of Participants Who Experience at Least One Adverse Drug Reactions (ADRs)
NCT02016183 (4) [back to overview]Changes From Baseline in Pulse Rate at Each Time Point
NCT02046395 (2) [back to overview]Change in the Level of Urinary Free Light Chains
NCT02046395 (2) [back to overview]Change in Urine Microalbumin Creatinine Ratio
NCT02183675 (7) [back to overview]Maximum Measured Concentration (Cmax) at Steady State for HCTZ
NCT02183675 (7) [back to overview]Maximum Measured Concentration (Cmax) at Steady State for Amlodipine
NCT02183675 (7) [back to overview]Area Under the Plasma Concentration Curve at Steady State for Telmisartan
NCT02183675 (7) [back to overview]Area Under the Plasma Concentration Curve at Steady State for HCTZ
NCT02183675 (7) [back to overview]Area Under the Plasma Concentration Curve at Steady State for Amlodipine
NCT02183675 (7) [back to overview]Amount of HCTZ Excreted in Urine at Steady State From 0 to 24 Hours
NCT02183675 (7) [back to overview]Maximum Measured Concentration (Cmax) at Steady State for Telmisartan
NCT02278471 (6) [back to overview]Medication Adherence-Percentage of Pills Taken
NCT02278471 (6) [back to overview]Systolic Blood Pressure
NCT02278471 (6) [back to overview]Systolic Blood Pressure
NCT02278471 (6) [back to overview]Medication Adherence
NCT02278471 (6) [back to overview]LDL Cholesterol
NCT02278471 (6) [back to overview]LDL Cholesterol
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target at 12 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target After 8 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among All Randomized Subjects After 8 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Change From Baseline Among All Randomized Subjects After 4 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among All Randomized Subjects After 12 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Change of Pulse Wave Velocity From Baseline at 2, 14 Weeks of Felodipine Sustained Release Alone.
NCT02336607 (12) [back to overview]The Percentage of Subjects Reaching Blood Pressure Target (Defined as < 140 / 90 mmHg) After 4 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Change of Pulse Wave Velocity at 12 Weeks Compare With Baseline Data of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Percentage of Subjects Reaching Blood Pressure Target (Defined as < 140 / 90 mmHg) After 8 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target at 4 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02336607 (12) [back to overview]The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target at 2 Weeks of Felodipine Sustained Release, Alone
NCT02336607 (12) [back to overview]The Percentage of Subjects Reaching Blood Pressure Target (Defined as < 140 / 90 mmHg) After 14 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.
NCT02412761 (1) [back to overview]The Number of Patients for Whom Each Drug is Selected as the Preferred Therapy
NCT02699125 (2) [back to overview]Brachial Artery Flow Mediated Dilation
NCT02699125 (2) [back to overview]24-h, Wake and Sleep Period Systolic and Diastolic Blood Pressure
NCT02710071 (1) [back to overview]24-h, Wake and Sleep Period Systolic and Diastolic Blood Pressure
NCT03031496 (16) [back to overview]Blood Urea Nitrogen (BUN) Levels at Indicated Time Points
NCT03031496 (16) [back to overview]Body Temperature Values at Indicated Time Points
NCT03031496 (16) [back to overview]Calcium, Chloride, Glucose, Magnesium, Potassium and Sodium Levels at Indicated Time Points
NCT03031496 (16) [back to overview]Creatinine, Direct Bilirubin and Total Bilirubin Levels at Indicated Time Points
NCT03031496 (16) [back to overview]Number of Participants With Adverse Events (AEs) and Serious AEs (SAEs) During Treatment Period
NCT03031496 (16) [back to overview]Percentage of AUC(0-inf) Obtained by Extrapolation (Percent AUCex) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma
NCT03031496 (16) [back to overview]Pulse Rate Values at Indicated Time Points
NCT03031496 (16) [back to overview]Respiratory Rate Values at Indicated Time Points
NCT03031496 (16) [back to overview]Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) Values at Indicated Time Points
NCT03031496 (16) [back to overview]Terminal Phase Half-life (T1/2) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma
NCT03031496 (16) [back to overview]Maximum Observed Concentration (Cmax) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma
NCT03031496 (16) [back to overview]Time of Occurrence of Cmax (Tmax) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma
NCT03031496 (16) [back to overview]Total Protein Levels at Indicated Time Points
NCT03031496 (16) [back to overview]AUC From Time Zero to Infinity (AUC[0-inf]) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma
NCT03031496 (16) [back to overview]Area Under the Curve (AUC) From Time Zero to the Time of the Last Quantifiable Concentration (AUC [0-t]) of Hydrochlorothiazide and Amiloride Hydrochloride
NCT03031496 (16) [back to overview]Alanine Aminotransferase (ALT), Alkaline Phosphatase (Alk.Phosph.) and Aspartate Aminotransferase (AST) Levels at Indicated Time Points
NCT03461003 (5) [back to overview]Number of Participants Who Reported That Side Effects From Medication Led Them to Discontinue Medication
NCT03461003 (5) [back to overview]Number of Participants Who Self-reported Adherence to Intervention
NCT03461003 (5) [back to overview]Patient Satisfaction With Intervention as Assessed by a Survey
NCT03461003 (5) [back to overview]Change in Mean 24-hour Ambulatory Systolic Blood Pressure
NCT03461003 (5) [back to overview]Change in Mean Wake Ambulatory Systolic Blood Pressure

Death From Any Cause in the Glycemia Trial.

"Time to death from any cause. Secondary measure for Glycemia Trial.~A finding of higher mortality in the intensive-therapy group led to an early discontinuation of therapy after a mean of 3.5 years of follow-up. Intensive arm participants were transitioned to standard arm strategy over a period of 0.2 year and followed for an additional 1.2 years to the planned end of the Glycemia Trial while participating in one of the other sub-trials (BP or Lipid)." (NCT00000620)
Timeframe: 4.9 years

Interventionparticipants (Number)
Glycemia Trial: Intensive Control391
Glycemia Trial: Standard Control327

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First Occurrence of a Major Cardiovascular Event (MCE); Specifically Nonfatal Heart Attack, Nonfatal Stroke, or Cardiovascular Death (Measured Throughout the Study) in the Glycemia Trial.

"Time to first occurrence of nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. This was the primary outcome measure in all three trials: Glycemia (all participants), Blood Pressure (subgroup of participants not in Lipid Trial), and Lipid (subgroup of participants not in Blood Pressure Trial).~In the Glycemia Trial, a finding of higher mortality in the intensive arm group led to an early discontinuation of therapy after a mean of 3.5 years of follow-up. Intensive arm participants were transitioned to standard arm strategy over a period of 0.2 year and followed for an additional 1.2 years to the planned end of the Glycemia Trial while participating in one of the other sub-trials (BP or Lipid) to their planned completion." (NCT00000620)
Timeframe: 4.9 years

Interventionparticipants (Number)
Glycemia Trial: Intensive Control503
Glycemia Trial: Standard Control543

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First Occurrence of Major Cardiovascular Event (MCE) in the Blood Pressure Trial.

Time to first occurrence of nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. Primary outcome for Blood Pressure Trial. (NCT00000620)
Timeframe: 4.7 years

Interventionparticipants (Number)
BP Trial: Intensive Control208
BP Trial: Standard Control237

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First Occurrence of Major Cardiovascular Event (MCE) in the Lipid Trial.

Time to first occurrence of nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death in Lipid Trial participants. (NCT00000620)
Timeframe: 4.7 years

Interventionparticipants (Number)
Lipid Trial: Fenofibrate291
Lipid Trial: Placebo310

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First Occurrence of MCE or Revascularization or Hospitalization for Congestive Heart Failure (CHF) in Lipid Trial.

Time to first occurrence of nonfatal myocardial infarction, nonfatal stroke, cardiovascular death, revascularization procedure or hospitalization for CHF in Lipid Trial participants. (NCT00000620)
Timeframe: 4.7 years

Interventionparticipants (Number)
Lipid Trial: Fenofibrate641
Lipid Trial: Placebo667

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Stroke in the Blood Pressure Trial.

Time to first occurrence of nonfatal or fatal stroke among participants in the BP Trial. (NCT00000620)
Timeframe: 4.7 years

Interventionparticipants (Number)
BP Trial: Intensive Control36
BP Trial: Standard Control62

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Time-to-event Analysis of Percentage of Patients With a Cardiovascular (CV) Mortality Event, Non-fatal Myocardial Infarction (MI), or Non-fatal Stroke

CV mortality was defined as death due to sudden cardiac death, fatal MI, fatal stroke, coronary intervention, congestive heart failure (CHF), or other CV causes. (NCT00170950)
Timeframe: For each patient, baseline to time of first CV mortality event, MI (non-fatal), or stroke (non-fatal) (or last exposure if no event occurred). (Median duration of exposure was 33.4 months. [25th to 75th percentiles: 21 to 41 months.])

InterventionPercentage of Patients with an Event (Number)
Benazepril/Amlodipine5.0
Benazepril/Hydrochlorothiazide6.3

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Time-to-event Analysis of Percentage of Patients With a Composite Cardiovascular (CV) Morbidity or Mortality Event

CV morbidity was defined as non-fatal myocardial infarction (MI), non-fatal stroke, hospitalization for unstable angina, resuscitated sudden death, or coronary revascularization procedure. CV mortality was defined as death due to MI, stroke, coronary intervention, congestive heart failure (CHF), sudden cardiac death, or other CV causes. (NCT00170950)
Timeframe: For each patient, baseline to time of first CV morbidity or mortality event (or last exposure if no event occurred). (Median duration of exposure was 33.4 months. [25th to 75th percentiles: 21 to 41 months.])

InterventionPercentage of Patients with an event (Number)
Benazepril/Amlodipine9.6
Benazepril/Hydrochlorothiazide11.8

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Time-to-event Analysis of Percentage of Patients With a Composite Cardiovascular (CV) Morbidity Event

Cardiovascular morbidity was defined as including any of the following events: non-fatal MI, non-fatal stroke, hospitalization for unstable angina, resuscitated sudden death, or coronary revascularization procedure (PCI or CABG). (NCT00170950)
Timeframe: For each patient, baseline to time of first CV morbidity event (or last exposure if no event occurred). (Median duration of exposure was 33.4 months. [25th to 75th percentiles: 21 to 41 months.])]

InterventionPercentage of Patients with an Event (Number)
Benazepril/Amlodipine8.6
Benazepril/Hydrochlorothiazide10.3

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Change From Baseline to Week 38 in the Carotid-femoral Pulse Wave Velocity (PWV)

PWV was determined from transcutaneous Doppler flow recordings and the foot-to-foot method triggered by the simultaneous ECG. Two simultaneous Doppler flow tracings were taken at the left common carotid and the right femoral artery in the groin with a linear array probe. The time delay (t) was measured between R wave of the ECG and the base of the flow waves recorded at these points, and averaged over 10 beats. The distance (D) traveled by the pulse wave was measured over body surface as the distance from the suprasternal notch to the carotid artery. PWV was calculated as PWV=D/t. (NCT00171054)
Timeframe: Baseline and Week 38

Interventionm/s (Least Squares Mean)
Valsartan 320 mg-1.9
Amlodipine 10 mg-1.7

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Changes in Mean Right Carotid Distensibility at Week 38

For carotid distensibility, the left and right bulbs and common carotid arteries are measured using tissue Doppler imaging with the linear array probe. Absolute diameter and diameter changes over the cardiac cycles will be recorded. Distensibility of each bulb will be calculated for three consecutive heart cycles and averaged and corrected for blood pressure. (NCT00171054)
Timeframe: Baseline and Week 38

Interventionpercent (Least Squares Mean)
Valsartan 320 mg-0.2
Amlodipine 10 mg0.0

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Changes in Mean Right Carotid Distensibility at Week 12

For carotid distensibility, the left and right bulbs and common carotid arteries are measured using tissue Doppler imaging with the linear array probe. Absolute diameter and diameter changes over the cardiac cycles will be recorded. Distensibility of each bulb will be calculated for three consecutive heart cycles and averaged and corrected for blood pressure. (NCT00171054)
Timeframe: Baseline and Week 12

Interventionpercent (Least Squares Mean)
Valsartan 320 mg-0.4
Amlodipine 10 mg0.1

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Change in Left Ventricular Mass Index (LVMI) and Diastolic Function Using Echocardiography From Baseline to Week 38

(NCT00171054)
Timeframe: Baseline and Week 38

Interventionpercent (Least Squares Mean)
Valsartan 320 mg-4.8
Amlodipine 10 mg-6.2

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Changes in Baroreflex Sensitivity as it Relates to Changes in Carotid Distensibility From Baseline to Week 12

The calculation of spontaneous baroflex sensitivity was obtained by the sequence method. Baroflex sequences are defined by at least three consecutive beats in which the systolic blood pressure and the RR interval of the following beat either both increased or decreased. The slope of each individual sequence is computed and the mean slope is determined as the average of all slopes within a given period of time and taken as the gain of the cardiac baroflex (BRSs). (NCT00171054)
Timeframe: Baseline and Week 12

InterventionEP (Least Squares Mean)
Valsartan 320 mg1.5
Amlodipine 10 mg-1.5

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Change From Baseline for Endothelial Function Measured by Brachial Artery Flow-mediated Vasodilatation (FMD) Using the Brachial Artery Reactivity Test (BART) at Week 12

Endothelial function will be assessed using high-resolution duplex ultrasound with wall tracking to measure FMD of the brachial artery during reactive hyperemia. FMD of the brachial artery in response to reactive hyperemia in the distal forearm (and glyceryl trinitrate as a non-endothelium dependent control) will be measured from B-mode ultrasound images using a standard 7 MHz linear array transducer and HDI 5000 system with edge detection. (NCT00171054)
Timeframe: Baseline and Week 12

Interventionpercent (Least Squares Mean)
Valsartan 320 mg-8.7
Amlodipine 10 mg-8.6

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Changes in Mean Left Carotid Distensibility at Week 12

For carotid distensibility, the left and right bulbs and common carotid arteries are measured using tissue Doppler imaging with the linear array probe. Absolute diameter and diameter changes over the cardiac cycles will be recorded. Distensibility of each bulb will be calculated for three consecutive heart cycles and averaged and corrected for blood pressure. (NCT00171054)
Timeframe: Baseline and Week 12

Interventionpercent (Least Squares Mean)
Valsartan 320 mg0.0
Amlodipine 10 mg0.0

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Change From Baseline for Endothelial Function Measured by Brachial Artery Flow-mediated Vasodilatation (FMD) Using the Brachial Artery Reactivity Test (BART) at End-point (Week 38)

Endothelial function will be assessed using high-resolution duplex ultrasound with wall tracking to measure FMD of the brachial artery during reactive hyperemia. FMD of the brachial artery in response to reactive hyperemia in the distal forearm (and glyceryl trinitrate as a non-endothelium dependent control) will be measured from B-mode ultrasound images using a standard 7 MHz linear array transducer and HDI 5000 system with edge detection. (NCT00171054)
Timeframe: Baseline and Week 38

Interventionpercent (Least Squares Mean)
Valsartan 320 mg-8.1
Amlodipine 10 mg-8.2

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Changes in Baroreflex Sensitivity as it Relates to Changes in Carotid Distensibility From Baseline to Week 38

The calculation of spontaneous baroflex sensitivity was obtained by the sequence method. Baroflex sequences are defined by at least three consecutive beats in which the systolic blood pressure and the RR interval of the following beat either both increased or decreased. The slope of each individual sequence is computed and the mean slope is determined as the average of all slopes within a given period of time and taken as the gain of the cardiac baroflex (BRSs). (NCT00171054)
Timeframe: Baseline and Week 38

InterventionEP (Least Squares Mean)
Valsartan 320 mg-2.0
Amlodipine 10 mg0.1

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Changes in Mean Left Carotid Distensibility at Week 38

For carotid distensibility, the left and right bulbs and common carotid arteries are measured using tissue Doppler imaging with the linear array probe. Absolute diameter and diameter changes over the cardiac cycles will be recorded. Distensibility of each bulb will be calculated for three consecutive heart cycles and averaged and corrected for blood pressure. (NCT00171054)
Timeframe: Baseline and Week 38

Interventionpercent (Least Squares Mean)
Valsartan 320 mg0.0
Amlodipine 10 mg0.1

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Changes in Central Blood Pressure, Evaluated by Applanation Tonometry From Baseline at Weeks 12 and 38

Central Blood Pressure was measured via applanation tonometry recordings of the common carotid artery and from brachial oscillometric recordings. The Simultaneously obtained carotid artery pressure and standard brachial artery blood pressure are computed to obtain the central systolic pressure. (NCT00171054)
Timeframe: Baseline, Week 12 and Week 38

,
Interventionmm Hg (Least Squares Mean)
Week 12Week 36
Amlodipine 10 mg-14.2-13.9
Valsartan 320 mg-9.1-11.1

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Change From Baseline in Post-ischemic Forearm Skin Reactive Hyperemia at Endpoint (Week 38)

Cutaneous blood flow was continuously recorded by a laser Doppler flowmeter. The laser Doppler flow probe was applied on the volar part of the right forearm with a plastic holder 10 cm proximal to the wrist. All measurements were made with a pressure cuff on the arm and inflated 20 mmHg above systolic BP and maintained for 2 min then rapidly deflated. All measurements were made in a quiet room with a patient in the supine position. The maximal reactive hyperemia was measured after cuff deflation, which allows measurement of the right forearm postischemic skin reactive hyperemia (SRH). (NCT00171054)
Timeframe: Week 38

InterventionPerfusion units (Least Squares Mean)
Valsartan 320 mg-9.7
Amlodipine 10 mg-94.6

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Change From Baseline in Post-ischemic Forearm Skin Reactive Hyperemia at Week 12

Cutaneous blood flow was continuously recorded by a laser Doppler flowmeter. The laser Doppler flow probe was applied on the volar part of the right forearm with a plastic holder 10 cm proximal to the wrist. All measurements were made with a pressure cuff on the arm and inflated 20 mmHg above systolic BP and maintained for 2 min then rapidly deflated. All measurements were made in a quiet room with a patient in the supine position. The maximal reactive hyperemia was measured after cuff deflation, which allows measurement of the right forearm postischemic skin reactive hyperemia (SRH). (NCT00171054)
Timeframe: Baseline and Week 12

InterventionPerfusion units (Least Squares Mean)
Valsartan 320 mg25.4
Amlodipine 10 mg-105.6

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Blood Pressure Response (Delta BP (After 18 Weeks of Medication - Baseline)).

(NCT00246519)
Timeframe: baseline to 18 weeks of treatment

InterventionmmHg (Mean)
Atenolol +HCTZ Arm-12.06
HCTZ + Atenolol-13.33

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Mean Change in Diastolic Blood Pressure Overall and for Each Treatment From Baseline to the Completion of the Treatment

(NCT00311155)
Timeframe: Baseline to ≤20 weeks

Interventionmm Hg (Mean)
Overall N=691OLM 20 mg N=688OLM 20 mg + HCTZ 12.5 mg N=580OLM 20 mg + HCTZ 25 mg N=446OLM 20 mg + HCTZ 25 mg + AML 5 mg N=296OLM 20 mg + HCTZ 25 mg + AML 10 mg N=176
Olmesartan+Hydrochlorothiazide,if Needed+Amlodipine, if Needed-15.73-6.44-10.15-13.04-14.03-14.47

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Mean Change in Systolic Blood Pressure Overall and for Each Treatment From Baseline to the Completion of the Treatment

(NCT00311155)
Timeframe: Baseline to ≤20 weeks

Interventionmm Hg (Mean)
Overall N=691OLM 20 mg N=688OLM 20 mg + HCTZ 12.5 mg N=580OLM 20 mg + HCTZ 25 mg N=446OLM 20 mg + HCTZ 25 mg + AML 5 mg N=296OLM 20 mg + HCTZ 25 mg + AML 10 mg N=176
Olmesartan+Hydrochlorothiazide,if Needed+Amlodipine, if Needed-29.58-11.97-19.55-24.51-27.06-28.02

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Percentage of Participants Who Achieved Normalized Blood Pressure Overall and for Each Treatment From Baseline to Completion of the Treatment During Which Blood Pressure Goals Were Achieved

Normalized blood pressure is defined as a mean sitting systolic blood (sBP) pressure at trough of <140 mmHg and mean sitting diastolic blood pressure (dBP)of <90 mmHg for non-diabetic patients or a mean sitting sBP at trough of <130 mmHg and mean sitting dBP <80 mmHg for diabetic patients. (NCT00311155)
Timeframe: Baseline to ≤20 weeks

InterventionPercentage of participants (Number)
Overall N=691OLM 20 mg N=688OLM 20 mg + HCTZ 12.5 mg N=580OLM 20 mg + HCTZ 25 mg N=446OLM 20 mg + HCTZ 25 mg + AML 5 mg N=296OLM 20 mg + HCTZ 25 mg + AML 10 mg N=176
Olmesartan+Hydrochlorothiazide,if Needed+Amlodipine, if Needed84.522.731.132.723.914.8

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Percentage of Participants Who Were Diastolic Responders Overall and for Each Treatment From Baseline to the Completion of Treatment During Which Blood Pressure Goals Were Achieved.

Diastolic responders were defined as a participant who is a normaliser or has a lowering of the mean sitting diastolic blood pressure of ≥10 mmHg at trough. (NCT00311155)
Timeframe: Baseline to ≤20 weeks

InterventionPercentage of participants (Number)
Overall N=691OLM 20 mg N=688OLM 20 mg + HCTZ 12.5 mg N=580OLM 20 mg + HCTZ 25 mg N=446OLM 20 mg + HCTZ 25 mg + AML 5 mg N=296OLM 20 mg + HCTZ 25 mg + AML 10 mg N=176
Olmesartan+Hydrochlorothiazide,if Needed+Amlodipine, if Needed93.336.652.448.633.420.4

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Percentage of Participants Who Were Systolic Responders Overall and for Each Treatment From Baseline to the Completion of the Treatment During Which Blood Pressure Goals Were Achieved

Systolic responders defined as a participant who is a normaliser or has a lowering of the mean sitting systolic blood pressure of ≥20 mmHg at trough (NCT00311155)
Timeframe: Baseline to ≤20 weeks

InterventionPercentage of Participants (Number)
Overall N=691OLM 20 mg N=688OLM 20 mg + HCTZ 12.5 mg N=580OLM 20 mg + HCTZ 25 mg N=446OLM 20 mg + HCTZ 25 mg + AML 5 mg N=296OLM 20 mg + HCTZ 25 mg + AML 10 mg N=176
Olmesartan+Hydrochlorothiazide,if Needed+Amlodipine, if Needed92.634.249.646.633.320.5

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The Percentage of Participants Treated to Target Blood Pressure Goals Overall and for Each Treatment Step From Baseline to Completion of Treatment During Which the Goal Was Achieved.

For non-diabetic participants the target seated blood pressure goals were: Systolic - ≤130 mm Hg; Diastolic - ≤85 mm Hg. For diabetic participants the target seated blood pressure goals were: Systolic - <130 mm Hg; Diastolic - <80 mm Hg. (NCT00311155)
Timeframe: Baseline to ≤20 weeks

InterventionPercentage of participants (Number)
Overall N=691OLM 20 mg N=688OLM 20 mg+HCTZ 12.5 mg N=580OLM 20 mg+HCTZ 25 mg N=446OLM 20 mg+HCTZ 25 mg+AML 5 mg N=296OLM 20 mg+HCTZ 25 mg+AML 10 mg N=176
Olmesartan+Hydrochlorothiazide,if Needed+Amlodipine, if Needed71.812.316.419.214.98.5

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Change From Baseline in Mean Sitting Systolic Blood Pressure to Week 12

(NCT00368277)
Timeframe: Baseline and Week 12

Interventionmm Hg (Least Squares Mean)
Aliskiren Based Treatment Regimen-13.96
Ramipril Based Treatment Regimen-11.64

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Percentage of Patients Achieving Blood Pressure Control at Weeks 12 and 36 Endpoints

Blood pressure control is defined as a mean sitting blood pressure < 140/90 mm Hg (NCT00368277)
Timeframe: Weeks 12 and 36

,
InterventionPercentage of participants (Number)
week 12 endpointweek 36 endpoint
Aliskiren Based Treatment Regimen46.365.6
Ramipril Based Treatment Regimen39.357.5

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Percentage of Patients With Cough

(NCT00368277)
Timeframe: Weeks 12 and 36

,
InterventionPercentage of Participants (Number)
Week 12Week 36
Aliskiren Based Treatment Regimen3.14.4
Ramipril Based Treatment Regimen9.914.2

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Change From Baseline in the Mean Sitting Diastolic Blood Pressure to Week 36

(NCT00368277)
Timeframe: Baseline and week 36

Interventionmm Hg (Least Squares Mean)
Aliskiren Based Treatment Regimen-8.24
Ramipril Based Treatment Regimen-7.02

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Change From Baseline in Mean Sitting Diastolic Blood Pressure

(NCT00386607)
Timeframe: Baseline and Month 18

InterventionmmHg (Mean)
Extension Treatment-18.3

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Change From Baseline in Mean Sitting Systolic Blood Pressure.

(NCT00386607)
Timeframe: Baseline and Weeks 2, 4, 6, 10, 14, 18, 28, 41 and 54

InterventionmmHg (Mean)
Week 2 (Visit 5)Week 4 (Visit 6)Week 6 (Visit 7)Week 10 (Visit 8)Week 14 (Visit 9)Week 18 (Visit 10)Week 28 (Visit 11)Week 41 (Visit 12)Week 54 (Visit 13)Endpoint (value at week 54 or LOCF)
Core Treatment-11.0-15.0-17.6-18.4-20.7-22.6-24.3-24.3-22.3-20.5

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Change From Baseline in Mean Sitting Diastolic Blood Pressure.

(NCT00386607)
Timeframe: Baseline and Weeks 2, 4, 6, 10, 14, 18, 28, 41, and 54

InterventionmmHg (Mean)
Week 2 (Visit 5)Week 4 (Visit 6)Week 6 (Visit 7)Week 10 (Visit 8)Week 14 (Visit 9)Week 18 (Visit 10)Week 28 (Visit 11)Week 41 (Visit 12)Week 54 (Visit 13)Endpoint (value at week 54 or LOCF)
Core Treatment-7.9-10.8-11.8-12.5-13.7-15.0-15.2-15.2-14.2-13.4

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Change From Baseline in Mean Sitting Systolic Blood Pressure

(NCT00386607)
Timeframe: Baseline and Month 18

InterventionmmHg (Mean)
Extension Treatment-28.8

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Overall Percentage of Patients With Adverse Events

(NCT00386607)
Timeframe: Month 12

Interventionpercentage of patients (Number)
Core Treatment- Aliskiren/Valsartan & Aliskiren/Valsartan/HCTZ76.2

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Overall Percentage of Patients With Adverse Events

adverse event data obtained from both the core study and the 6 month extension study. (NCT00386607)
Timeframe: Month 18

Interventionpercentage of patients (Number)
Core and Extension Treatment - Aliskiren/Valsartan/HCTZ61.6

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Percentage of Patients Achieving Blood Pressure Control Target of < 140/90 mmHg in Extension Treatment

(NCT00386607)
Timeframe: Month 18

InterventionPercentage of patients (Number)
Extension Treatment86.6

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Percentage of Patients Achieving Blood Pressure Control Target of < 140/90 mmHg

(NCT00386607)
Timeframe: .Weeks 2, 4, 6, 10, 14, 18, 28, 41, and 54

InterventionPercentage of patients (Number)
Week 2 (Visit 5)Week 4 (Visit 6)Week 6 (Visit 7)Week 10 (Visit 8)Week 14 (Visit 9)Week 18 (Visit 10)Week 28 (Visit 11)Week 41 (Visit 12)Week 54 (Visit 13)Endpoint (value at week 54 or LOCF)
Core Treatment32.845.952.460.868.776.477.978.271.766.9

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Mean Post-treatment Microcirculation at NaCl Injected Sites

10 µl of NaCl was injected intra-dermally at 2 sites on the forearms. Microcirculation was measured using laser doppler velocimetry before and 12 times in the 30 minutes following injection. The mean difference of the 12 post-injection measurements to the pre-injection measurement was calculated. A mean for the 2 NaCl sites was calculated. Microcirculation was measured in perfusion units which is an arbitrary measure specific to each laser doppler scanner. (NCT00396656)
Timeframe: At end of each treatment period (Week 21 and Week 43)

InterventionPerfusion units (Mean)
Valsartan44.78
Atenolol + Hydrochlorothiazide50.96

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Difference in Mean Post-treatment Microcirculation at Acetylcholine (ACH) Plus L-NMMA Injected Sites Compared to NaCl Injected Sites

10 µl of acetylcholine (ACH) at 3 concentrations (10-7, 10-8, 10-9 M) plus 10 µl L-NMMA (10-6 M) was injected intra-dermally at 3 sites on the forearms. NaCl was injected at 2 sites. Microcirculation was measured using laser doppler velocimetry before and 12 times in the 30 minutes following injection. The mean difference of the 12 post-injection measurements to the pre-injection measurement was calculated. Means for the 3 ACH and the 2 NaCl sites were calculated and compared. Microcirculation was measured in perfusion units which is an arbitrary measure specific to each laser doppler scanner. (NCT00396656)
Timeframe: At end of each treatment period (Week 21 and Week 43)

InterventionPerfusion units (Mean)
Valsartan-9.11
Atenolol + Hydrochlorothiazide-5.60

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Difference in Mean Post-treatment Microcirculation at Acetylcholine (ACH) Injected Sites Compared to NaCl Injected Sites

10 µl of acetylcholine (ACH) at 3 concentrations (10-7, 10-8, 10-9 M) was injected intra-dermally at 3 sites on the forearms. NaCl was injected at 2 sites on the forearms. Microcirculation was measured using laser doppler velocimetry before and 12 times in the 30 minutes following injection. The mean difference of the 12 post-injection measurements to the pre-injection measurement was calculated. Means for the 3 ACH and the 2 NaCl sites were calculated and compared. Microcirculation was measured in perfusion units which is an arbitrary measure specific to each laser doppler scanner. (NCT00396656)
Timeframe: At end of each treatment period (Week 21 and Week 43)

InterventionPerfusion units (Mean)
Valsartan61.21
Atenolol + Hydrochlorothiazide61.04

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Difference in Mean Post-treatment Microcirculation at a Sodium Nitroprusside Injected Site Compared to NaCl Injected Sites

10 µl of sodium nitroprusside at a concentration of 10-7 M was injected intra-dermally at 1 site on the forearms. NaCl was injected at 2 sites on the forearms. Microcirculation was measured using laser doppler velocimetry before and 12 times in the 30 minutes following injection. The mean difference of the 12 post-injection measurements to the pre-injection measurement was calculated. A mean for the 2 NaCl sites was calculated and compared to the sodium nitroprusside mean. Microcirculation was measured in perfusion units which is an arbitrary measure specific to each laser doppler scanner. (NCT00396656)
Timeframe: At end of each treatment period (Week 21 and Week 43)

InterventionPerfusion units (Mean)
Valsartan120.65
Atenolol + Hydrochlorothiazide128.14

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Arterial Pressure Waveform Augmentation Index at the End of Treatment

Using applanation tonometry, the arterial pulse form measured at the wrist was analyzed using computerized pulse wave analysis. The arterial pressure waveform has two components; the first is the forward traveling wave when the left ventricle contracts and the second is the reflected wave returning from the periphery. The augmentation index is the ratio of the first and second systolic peaks and is used as a surrogate measure of arterial stiffness. (NCT00396656)
Timeframe: At end of each treatment period (Week 21 and Week 43)

InterventionRatio (Mean)
Valsartan139.05
Atenolol + Hydrochlorothiazide144.51

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Arterial Pressure Waveform Pulse Wave Velocity at the End of Treatment

Using applanation tonometry, the arterial pulse form measured at the wrist was analyzed using computerized pulse wave analysis. The arterial pressure waveform has two components; the first is the forward traveling wave when the left ventricle contracts and the second is the reflected wave returning from the periphery. Pulse wave velocity is the speed of the forward traveling wave and can be used as a measure of arterial stiffness since the more rigid the wall of the artery, the faster the wave moves. (NCT00396656)
Timeframe: At end of each treatment period (Week 21 and Week 43)

InterventionMeters per second (Mean)
Valsartan8.07
Atenolol + Hydrochlorothiazide7.60

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Overall Percentage of Patients With Adverse Events

(NCT00402103)
Timeframe: 52 weeks

InterventionPercentage of Participants (Number)
Aliskiren 150mg/ Amlodipine 5mg Alone23.6
Aliskiren 300mg/ Amlodipine 10mg Alone71.2
Aliskiren 300mg/ Amlodipine 10mg/ HCTZ57.0

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Percentage of Patients Achieving a Response in Mean Sitting Diastolic Blood Pressure (msDBP)

(NCT00402103)
Timeframe: Baseline, Week 2, Week 10, Week 28 and Week 54

,
InterventionPercentage of patients (Number)
Week 2 (Visit 5)Week 10 (Visit 8)Week 28 (Visit 10)Week 54 (Visit 12)Week 54 (Visit 12) (LOCF)
Aliskiren/Amlodipine61.296.895.993.290.6
Aliskiren/Amlodipine/HCTZ38.461.685.289.284.9

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Percentage of Patients Achieving a Blood Pressure Control Target of <140/90 mmHg

(NCT00402103)
Timeframe: Baseline, Week 2, Week 10, Week 28 and Week 54

,
InterventionPercentage of patients (Number)
Week 2 (Visit 5)Week 10 (Visit 8)Week 28 (Visit 10)Week 54 (Visit 12)Week 54 (Visit 12) (LOCF)
Aliskiren/Amlodipine35.388.088.282.077.3
Aliskiren/Amlodipine/HCTZ8.116.356.862.258.1

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Change in Mean Sitting Diastolic Blood Pressure (msDBP)From Baseline to the Indicated Time Points

(NCT00402103)
Timeframe: Baseline, Week 2, Week 4, Week 6, Week 10, Week 14, Week 28, Week 41 and Week 54

,
Interventionmm Hg (Mean)
Week 2 (Visit 5)Week 4 (Visit 6)Week 6 (Visit 7)Week 10 (Visit 8)Week 14 (Visit 9)Week 28 (Visit 10)Week 41 (Visit 11)Week 54 (Visit 12)Week 54 (Visit 12) (LOCF)
Aliskiren/Amlodipine-8.7-14.0-15.7-16.3-17.1-16.7-17.0-16.3-15.7
Aliskiren/Amlodipine/HCTZ-5.9-11.9-11.5-9.3-13.1-14.7-15.4-15.3-14.2

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Change From Baseline to Week 12 in Ambulatory BP Measurement (Systolic)During the Last 2 Hours of the Last (Week 12) 24-hour Dosing Period.

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
Overall Study Population-18.6

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Change From Baseline to Week 12 in Ambulatory BP Measurement (Systolic)During the Last 4 Hours of the Last (Week 12 ) 24-hour Dosing Period.

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
Overall Study Population-18.2

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Change From Baseline to Week 12 in Ambulatory BP Measurement (Systolic)During the Last 6 Hours of the Last (Week 12 ) 24-hour Dosing Period.

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
Overall Study Population-18.6

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Change From Baseline to Week 12 in Mean 24-hour Ambulatory BP (Diastolic)

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
Overall Study Population-11.1

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Change From Baseline to Week 12 in Systolic BP (SBP) as Measured by 24-hour ABPM.

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
Overall Study Population-20.4

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Change in Ambulatory Blood Pressure (Diastolic) From Baseline to Week 12 During the Last 2 Hours of the Last (Week 12 ) 24-hour Dosing Period.

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 Weeks

Interventionmm Hg (Mean)
Overall Study Population-10.6

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Change From Baseline to Week 12 in Mean Daytime and Nighttime Ambulatory Blood Pressure Measurement (Systolic).

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
DaytimeNighttime
Overall Study Population-22.3-18.8

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Change in Daytime and Nighttime Ambulatory Blood Pressure (Diastolic) From Baseline to Week 12

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
DaytimeNighttime
Overall Study Population-12.0-10.2

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Change in Ambulatory BP (Diastolic) From Baseline to Week 12 During the Last (Week 12 ) 4 and 6 Hours of the Last 24-hour Dosing Period.

Participants had a 24-hour ambulatory blood pressure session at baseline and after 12 weeks of treatment. This outcome measure pooled all participants regardless of their titration history during the study. (NCT00403481)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
4 hours6 hours
Overall Study Population-10.7-10.8

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Number of Subjects Who Achieved Mean Nighttime (10pm - 6am) Ambulatory Blood Pressure of <140/90 mm Hg, Systolic Blood Pressure <140 mm Hg, and Diastolic Blood Pressure <90 mm Hg After 12 Weeks of Active Treatment.

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionparticipants (Number)
BP<140/90 mm HgSBP<140 mm HgDBP<90 mm Hg
Overall Study143143149

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Change From Baseline in Mean 24-hour Ambulatory Diastolic Blood Pressure After 12 Weeks of Active Treatment.

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Mean)
Overall Study-12.3

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Change From Baseline in Mean 24-hour Ambulatory Systolic Blood Pressure After 12 Weeks of Active Treatment

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Mean)
Overall Study-25.7

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Change From Baseline in Mean Daytime (8am-4pm) and Mean Nighttime (10 Pm-6am) Ambulatory Blood Pressure Monitored Diastolic Blood Pressure After 12 Weeks of Active Treatment

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Mean)
DaytimeNighttime
Overall Study-13.0-11.5

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Change From Baseline in Mean Daytime (8am-4pm) and Mean Nighttime (10pm-6am)Ambulatory Systolic Blood Pressure After 12 Weeks of Active Treatment

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Mean)
DaytimeNighttime
Overall Study-26.5-24.4

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Number of Subjects Who Achieved Mean 24-hour Ambluatory Blood Pressure of <140/90 mm Hg, Systolic Blood Pressure <140 mm Hg, and Diastolic Blood Pressure <90 mm Hg After 12 Weeks of Active Treatment

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionparticipants (Number)
BP<140/90 mm HgSBP<140 mm HgDBP<90 mm Hg
Overall Study133133149

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Number of Subjects Who Achieved Mean Daytime (8am - 4pm) Ambulatory Blood Pressure of <140/90 mm Hg, Systolic Blood Pressure <140 mm Hg, and Diastolic Blood Pressure <90 mm Hg After 12 Weeks of Active Treatment.

All participants started the treatment arm with 20 mg olmesartan medoxomil (Olm). If their blood pressure was not controlled, participants were titrated at 3-week intervals to: Olm 40 mg, then, if needed Olm 40 mg + hydrochlorothiazide (HCTZ) 12.5 mg, then, if needed Olm 40 mg + HCTZ 25 mg This outcome measure included all participants at the end of the 12-week treatment period regardless of whether or not they were titrated. They had to have both baseline and 12-week ambulatory blood pressure measurements. (NCT00412932)
Timeframe: baseline to 12 weeks

Interventionparticipants (Number)
BP<140/90 mm HgSBP<140 mm HgDBP<90 mm Hg
Overall Study120120145

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Change in Mean Trough Sitting Systolic Blood Pressure From Week 8(Baseline) to Week 12.

Change = Week 12 - Week 8 (baseline). (NCT00430508)
Timeframe: 4 weeks, change = week 12 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-13.16
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-10.90
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-9.65
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-6.60

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Number of Patients Achieving Target Blood Pressure at Week 16

Target Blood Pressure is diastolic blood pressure (dBP) < 90 mmHg and systolic blood pressure (sBP) < 140 mmHg for non-diabetics, and dBP < 80 mmHg and sBP < 130 mmHg for diabetics (NCT00430508)
Timeframe: 8 weeks

Interventionparticipants (Number)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo59
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo110
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo88
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo68

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Change in Mean Trough Sitting Systolic Blood Pressure From Week 8(Baseline) to Week 16.

Change = Week 16 - Week 8 (baseline). (NCT00430508)
Timeframe: 8 weeks, change = week 16 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-16.17
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-13.52
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-11.46
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-8.85

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Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 16

Change = Week 16 - Week 8 (baseline). (NCT00430508)
Timeframe: 8 weeks, change = week 16 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-11.16
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-9.13
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-8.10
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-5.66

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Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 12.

Change = Week 12 - Week 8 (baseline). (NCT00430508)
Timeframe: 4 weeks, change = week 12 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-8.74
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-7.72
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-6.66
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-4.47

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Change in Mean Night-time Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16.

Change = Week 16 - Week 8 (baseline). (NCT00430508)
Timeframe: 8 weeks, change = week 16 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-7.9
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-4.5
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-4.2
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-2.3

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Change in Mean Daytime Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16.

Change = Week 16 - Week 8 (baseline). (NCT00430508)
Timeframe: 8 weeks, change = week 16 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-7.0
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-5.5
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-4.0
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-1.8

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Change in Mean 24-hour Ambulatory Blood Pressure Monitoring Diastolic Blood Pressure From Week 8(Baseline) to Week 16.

Change = Week 16 - Week 8 (baseline). (NCT00430508)
Timeframe: 8 weeks, change = week 16 - week 8

Interventionmm Hg (Mean)
OM/HCTZ 40/25mg + 20/12.5 Matching Placebo-7.2
OM/HCTZ 40/12.5mg + 20/12.5 Matching Placebo-5.3
OM/HCTZ 20/12.5mg + 40/0 Matching Placebo-4.1
OM/HCTZ 40/0mg + 20/12.5 Matching Placebo-2.0

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Change From Baseline in Mean Diastolic Blood Pressure (DBP) After 12 Weeks of Randomized Treatment as Measured by Omron Device.

Change from study baseline (average of triplicate DBP measurements at the last 2 qualifying visits during placebo run-in period) in DBP to the end of 12 weeks of randomized treatment using a last observation carried forward (LOCF) approach. (NCT00430638)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Least Squares Mean)
Placebo Group-0.8
Olmesartan Group-12.1

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Black Participants.

(NCT00430638)
Timeframe: Baseline to week 12

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-21.3-12.5

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Females.

The difference in the change from baseline to week 12 in seated blood pressure for females in the olmesartan group vs. the placebo group was analyzed. (NCT00430638)
Timeframe: Baseline to week 12

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-21.6-12.0

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Males.

The difference in the change from baseline to week 12 in seated systolic and diastolic blood pressure for males in the olmesartan group vs. the placebo group was analyzed. (NCT00430638)
Timeframe: Baseline to week 12

Interventionmm Hg (Least Squares Mean)
Systolic Blood PressureDiastolic Blood Pressure
Olmesartan vs. Placebo-22.6-13.5

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Non-Black Participants.

(NCT00430638)
Timeframe: Baseline to 12 weeks

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-22.3-12.8

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Participants Greater Than or Equal to 65 Years Old.

(NCT00430638)
Timeframe: Baseline to 12 weeks

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-16.1-9.0

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Change From Baseline in Mean Systolic Blood Pressure (SBP) After 12 Weeks of Randomized Treatment as Measured by Omron Device.

The change from baseline in mean systolic blood pressure (SBP) after 12 weeks of randomized treatment was compared between the olmesartan based treatment group and the placebo treatment group. (NCT00430638)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Least Squares Mean)
Placebo-0.1
Olmesartan Group-22.3

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Participants Less Than 65 Years Old.

(NCT00430638)
Timeframe: Baseline to 12 weeks

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-23.8-13.6

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Stage 1 Hypertensives

(NCT00430638)
Timeframe: Baseline to 12 weeks

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-22.1-12.2

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The Difference in the Change From Baseline to Week 12 in Seated Systolic and Diastolic Blood Pressure Between the Olmesartan Group and the Placebo Group for Stage 2 Hypertensives

(NCT00430638)
Timeframe: Baseline to 12 months

Interventionmm Hg (Least Squares Mean)
Systolic blood pressureDiastolic blood pressure
Olmesartan vs. Placebo-22.5-13.2

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Change in Mean Trough Sitting Diastolic Blood Pressure

"Change in mean trough sitting diastolic Blood Pressure between OM/HCTZ 20/25 mg vs. 40/25 mg, in those patients inadequately controlled on OM 40 mg monotherapy, after eight weeks of double blind treatment, as compared to baseline.~Change = Week 16 - Week 8 (baseline)." (NCT00430950)
Timeframe: 8 weeks

Interventionmm Hg (Mean)
OM/HCTZ 40/25 mg + 20/25 mg Matching Placebo-11.16
OM/HCTZ 20/25 mg + 40/25 mg Matching Placebo-10.45

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Number of Participants Achieving Blood Pressure Goal.

(NCT00430950)
Timeframe: 8 weeks

Interventionparticipants (Number)
OM/HCTZ 40/25 mg + 20/25 mg Matching Placebo260
OM/HCTZ 20/25 mg + 40/25 mg Matching Placebo255

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Change in Sitting Systolic Blood Pressure 4 Weeks and 8 Weeks After Baseline.

4 weeks Change = Week 12 - Week 8 (baseline). 8 weeks Change = Week 16 - Week 8 (baseline). (NCT00430950)
Timeframe: 8 weeks

,
Interventionmm Hg (Mean)
Change from baseline (Week 8) to Week 16 in sBPChange from baseline (Week 8) to Week 12 in sBP
OM/HCTZ 20/25 mg + 40/25 mg Matching Placebo-17.09-13.80
OM/HCTZ 40/25 mg + 20/25 mg Matching Placebo-17.41-14.07

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Change in Daytime, Nighttime and 24-hour Blood Pressure Evaluated by Ambulatory Blood Pressure Monitoring 8 Weeks After Baseline.

Change = Week 16 - Week 8 (baseline). (NCT00430950)
Timeframe: 8 weeks

,
Interventionmm Hg (Mean)
Change from Week 8 to Wk 16 in mean 24-hr ABPM dBPChange from Week 8 to wk16 in daytime ABPM dBPChange from Week 8 to wk16 in nighttime ABPM dBPChange from Week 8 to wk16 in mean 24-hr ABPM sBPChange from Week 8 to wk16 in daytime ABPM sBPChange from Week 8 to wk16 in nighttime ABPM sBP
OM/HCTZ 20/25 mg + 40/25 mg Matching Placebo-7.6-7.7-7.0-12.0-12.3-10.7
OM/HCTZ 40/25 mg + 20/25 mg Matching Placebo-9.2-9.3-8.6-14.7-15.0-13.4

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Change in Mean Trough Sitting Diastolic Blood Pressure From Week 8(Baseline) to Week 12

Change = Week 12 - Week 8 (baseline). (NCT00430950)
Timeframe: 4 weeks

Interventionmm Hg (Mean)
OM/HCTZ 40/25 mg + 20/25 mg Matching Placebo-9.32
OM/HCTZ 20/25 mg + 40/25 mg Matching Placebo-8.83

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Change in Sitting Systolic Blood Pressure (SBP) From Baseline to the End of the Study (Baseline to 8 Weeks)

Change (reduction) in sitting SBP at the end of the study, when compared to sitting SBP at baseline. (NCT00434967)
Timeframe: 8 weeks

Interventionmm Hg (Least Squares Mean)
Placebo-3.7
Candesartan 32 mg-13.1
HCT 25 mg-11.6
Candesartan/HCT 32/25 mg-21.4

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The Number of Patients With Controlled Sitting DBP and Sitting SBP in Each Treatment Group at the End of the Study

Controlled sitting SBP and sitting DBP are defined as having sitting SBP < 140 mmHg and sitting DBP < 90 mmHg at the end of the study (NCT00434967)
Timeframe: 8 weeks

Interventionparticipants (Number)
Placebo8
Candesartan 32 mg198
HCT 25 mg168
Candesartan/HCT 32/25 mg304

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Change in Sitting Diastolic Blood Pressure (DBP) From Baseline to the End of the Study (From Baseline to 8 Weeks).

Change (reduction) in sitting DBP at the end of the study, when compared to sitting DBP at baseline. (NCT00434967)
Timeframe: 8 weeks

Interventionmm Hg (Least Squares Mean)
Placebo-3.3
Candesartan 32 mg-9.3
HCT 25 mg-7.7
Candesartan/HCT 32/25 mg-13.9

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Change From Baseline in Postprandial Non-esterified Fatty Acids

After a 75 gram anhydrous glucose challenge 2 hours after an oral glucose tolerance test (NCT00439738)
Timeframe: Week 16

,
Interventionmg/dL (Mean)
Baseline visit (0 minutes)Week 16 (0 minutes)Change from baseline to week 16 (0 minutes)Baseline visit (120 minutes)Week 16 (120 minutes)Change from baseline to week 16 (120 minutes)
HCTZ +Amlodipine0.470.470.000.100.10-0.01
Valsartan/HCTZ (Hydrochlorothiazide)0.450.460.010.110.10-0.01

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Change in Mean Sitting Systolic Blood Pressure (MSSBP)

(NCT00439738)
Timeframe: Baseline to Week 8

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from baseline
HCTZ +Amlodipine159.0137.5-21.5
Valsartan/HCTZ (Hydrochlorothiazide)159.7131.2-28.6

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Number of Patients Achieving Blood Pressure (BP)Control by Visit (< 130/80 mm Hg)

Mean sitting systolic blood pressure/mean sitting diastolic blood pressure < 130/80 mm Hg (NCT00439738)
Timeframe: Week 4, 8, 12, 16, End of Study (for patients that did not complete the last visit at week 16)

,
Interventionparticipants (Number)
Week 4Week 8Week 12Week 16End of Study
HCTZ +Amlodipine1823466568
Valsartan/HCTZ (Hydrochlorothiazide)3359576268

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Change From Baseline in Postprandial Glucose

After a 75 gram anhydrous glucose challenge 2 hours after an oral glucose tolerance test (NCT00439738)
Timeframe: Week 16

,
Interventionmg/dL (Mean)
Baseline visit (0 minutes)Week 16 (0 minutes)Change from baseline to week 16 (0 minutes)Baseline visit (120 minutes)Week 16 (120 minutes)Change from baseline to week 16 (120 minutes)
HCTZ +Amlodipine99.4102.83.4127.7146.518.9
Valsartan/HCTZ (Hydrochlorothiazide)98.098.1-0.5123.9126.32.1

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Change From Baseline in Postprandial Insulin

After a 75 gram anhydrous glucose challenge 2 hours after an oral glucose tolerance test (NCT00439738)
Timeframe: Week 16

,
Interventionmg/dL (Mean)
Baseline visit (0 minutes)Week 16 (0 minutes)Change from baseline to week 16 (0 minutes)Baseline visit (120 minutes)Week 16 (120 minutes)Change from baseline to week 16 (120 minute)
HCTZ +Amlodipine20.3723.623.6795.95120.0128.07
Valsartan/HCTZ (Hydrochlorothiazide)19.6623.453.4192.04116.0424.68

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Change in Mean Sitting Diastolic Blood Pressure (MSDBP)

(NCT00439738)
Timeframe: Baseline to Weeks 4, 8, 12 and 16

,
Interventionmm Hg (Mean)
BaselineWeek 4Week 8Week 12Week 16Change from baseline to week 16
HCTZ +Amlodipine93.687.685.182.880.9-12.7
Valsartan/HCTZ (Hydrochlorothiazide)94.985.781.981.180.8-14.0

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Number of Patients Achieving Blood Pressure (BP) Control by Visit (< 140/90 mm Hg)

Mean sitting systolic blood pressure/mean sitting diastolic blood pressure < 140/90 mm Hg (NCT00439738)
Timeframe: Weeks 4, 8, 12 16 and End of Study (for patients that did not complete the last visit at week 16)

,
Interventionparticipants (Number)
Week 4Week 8Week 12Week 16End of study
HCTZ +Amlodipine69102112140146
Valsartan/HCTZ (Hydrochlorothiazide)91123122124133

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Change From Baseline to End of Study in Levels of N-terminal Pro-B Type Natriuretic Peptide (NT-proBNP)

(NCT00446563)
Timeframe: Baseline to week 52

Interventionpg/ml (Mean)
Valsartan and Amlodipine-4.5
Losartan and HCTZ-40.1

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Change From Baseline to End of Study in Levels of High-sensitivity C-reactive Protein (Hs-CRP)

(NCT00446563)
Timeframe: Baseline to week 52

Interventionmg/l (Mean)
Valsartan and Amlodipine0.8
Losartan and HCTZ-2.1

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Change From Baseline in Left Ventricular Mass Index (LVMI) Measured Via Magnetic Resonance Imaging (MRI)

(NCT00446563)
Timeframe: Baseline to week 52

Interventiong/m˄2 (Mean)
Valsartan and Amlodipine-7.1
Losartan and HCTZ-9.1

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Change From Baseline to the End of Study in Interventricular Septum Thickness (IVS) Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionmm (Mean)
Valsartan and Amlodipine-1.1
Losartan and HCTZ-0.6

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Percentage of Participants Who Experienced Adverse Events (AEs)

An adverse event was the appearance or worsening of any undesirable sign, symptom, or medical condition occurring after obtaining informed consent even if the event was not considered to be related to study drug. Medical conditions/diseases present before obtaining informed consent were only considered adverse events if they worsened after study start. Abnormal laboratory values or test results constituted adverse events only if they induced clinical signs or symptoms, required study drug discontinuation or required therapy. (NCT00446563)
Timeframe: Baseline to week 52

InterventionPercentage of participants (Number)
Valsartan and Amlodipine69.8
Losartan and HCTZ68.1

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Percentage of Participants Achieving Target Blood Pressure at Week 52

Target blood pressure defined as having a mean sitting systolic blood pressure (MSSBP) < 140 mm Hg and a mean sitting diastolic blood pressure (MSDBP) < 90 mm Hg. (NCT00446563)
Timeframe: Week 52

InterventionPercentage of participants (Number)
Valsartan and Amlodipine53.5
Losartan and HCTZ14.9

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Change From Baseline to the End of Study in Left Atrial (LA) Area Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventioncm˄2 (Mean)
Valsartan and Amlodipine-0.6
Losartan and HCTZ-1.0

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Change From Baseline to the End of Study in the Ascending Aortic Diameter Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionmm (Mean)
Valsartan and Amlodipine0.1
Losartan and HCTZ-0.8

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Change From Baseline to the End of Study in Left Ventricular End-Systolic Volume (LVESV) Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionml (Mean)
Valsartan and Amlodipine0.4
Losartan and HCTZ-1.5

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Change From Baseline to the End of Study in Posterior Wall Thickness Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionmm (Mean)
Valsartan and Amlodipine-0.4
Losartan and HCTZ-0.3

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Change From Baseline to the End of Study in Left Ventricular End-diastolic Volume (LVEDV) Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionml (Mean)
Valsartan and Amlodipine0.1
Losartan and HCTZ-6.4

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Change From Baseline to the End of Study in Left Ventricular Ejection Fraction (LVEF) Assessed by MRI

Ejection fraction is a measurement of the percentage of blood that is pumped out of a filled ventricle with each heartbeat. (NCT00446563)
Timeframe: Baseline to week 52

InterventionPercentage (Mean)
Valsartan and Amlodipine-0.8
Losartan and HCTZ-0.4

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Change From Baseline to the End of Study in Left Ventricular End-diastolic Volume (LVEDV) Normalized to Body Surface Area Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionml (Mean)
Valsartan and Amlodipine0.0
Losartan and HCTZ-3.0

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Change From Baseline to the End of Study in Left Ventricular End-Systolic Volume (LVESV) Normalized to Body Surface Area Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventionml (Mean)
Valsartan and Amlodipine0.2
Losartan and HCTZ-0.8

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Change From Baseline to the End of Study in Left Ventricular Mass Index (LVMI) Normalized to Body Surface Area Assessed by MRI

(NCT00446563)
Timeframe: Baseline to week 52

Interventiong/m˄2 (Mean)
Valsartan and Amlodipine-3.5
Losartan and HCTZ-4.4

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Change in Reactive Hyperemic Index by Period (Carvedilol CR + Lisinopril vs. Lisinopril + HCTZ)

Reactive hyperemic index is a measure of endothelial function. This is measured by the ratio of post-occlusion blood volume flow versus the baseline blood volume flow. The outcome reported is the change in this ratio after the first intervention phase compared to after the second intervention phase. (NCT00459056)
Timeframe: Change from three months to seven months

InterventionRatio (Mean)
Carvedilol CR + Lisinopril, Then Lisinopril +HCTZ-0.26
Lisinopril + HCTZ, Then Carvedilol CR + Lisinopril-0.14

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24h Urine Volume

urine volume in mL/d (NCT00478335)
Timeframe: 4-days

,
Interventionurine volume in mL/d (Mean)
Period 1Period 2
Experimental First Then Standard64756652
Standard First Then Experimental41784188

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Diastolic Blood Pressure (DBP) Mean Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug

(NCT00496834)
Timeframe: Baseline and 24 weeks

Interventionmm Hg (Mean)
Losartan-8.43
Carvedilol-7.81

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Pulse Wave Velocity (PWV) Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug

Analysis was performed in the modified intention to treat (mITT) population. (NCT00496834)
Timeframe: Baseline and 24 Weeks

Interventionmeters/second (Mean)
Losartan0.28
Carvedilol-0.12

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PWV Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug

Analysis was performed in the per protocol (PP) population which additionally excludes certain protocol violations as described in the analysis plan. (NCT00496834)
Timeframe: Baseline and 24 Weeks

Interventionmeters/second (Mean)
Losartan0.16
Carvedilol-0.20

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Systolic Blood Pressure (SBP) Mean Changes From Baseline (Visit 2) to 24 Weeks (Visit 6) After the Administration of the Study Drug

(NCT00496834)
Timeframe: Baseline and 24 weeks

Interventionmm Hg (Mean)
Losartan-15.08
Carvedilol-14.81

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Percentage of Patients Who Achieved Normalized Blood Pressure During the Extension Phase of the Study

Normalized Blood Pressure was defined as a msSBP < 140 mmHg and/or a msDBP < 90 mmHg. (NCT00523744)
Timeframe: Baseline Phase 3 (Week 8) to end of Phase 3 (Week 12)

InterventionPercentage of participants (Number)
msSBP < 140 mmHgmsDBP < 90 mmHg
Amlodipine+Valsartan+HCTZ - Phase 359.383.5

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Percentage of Patients Who Achieved Normalized Blood Pressure During the Core Phase of the Study

Normalized Blood Pressure was defined as a msSBP < 140 mmHg and/or a msDBP < 90 mmHg. (NCT00523744)
Timeframe: Baseline Phase 2 (Week 4) to end of Phase 2 (Week 8)

InterventionPercentage of participants (Number)
msSBP < 140 mmHgmsDBP < 90 mmHg
Amlodipine+Valsartan - Phase 244.672.6

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Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Extension Phase of the Study

Blood pressure response was defined as msSBP < 140 mmHg or a 20 mmHg decrease in msSBP at the end of Phase 3 compared to Baseline in Phase 3 or a msDBP < 90 mmHg or a 10 mmHg decrease in msDBP at the end of Phase 3 compared to Baseline in Phase 3. (NCT00523744)
Timeframe: Baseline of Phase 3 (Week 8) to end of Phase 3 (Week 12)

InterventionPercentage of participants (Number)
msSBP responsemsDBP response
Amlodipine+Valsartan+HCTZ - Phase 361.583.5

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Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Core Phase of the Study

Blood pressure response was defined as msSBP < 140 mmHg or a 20 mmHg decrease in msSBP at the end of Phase 2 (Week 8) compared to Baseline in Phase 2 (week 4) or a msDBP < 90 mmHg or a 10 mmHg decrease in msDBP at the end of Phase 2 compared to Baseline in Phase 2. (NCT00523744)
Timeframe: Baseline of Phase 2 (Week 4) to end of Phase 2 (Week 8)

InterventionPercentage of participants (Number)
msSBP responsemsDBP response
Amlodipine+Valsartan - Phase 247.473.1

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Change in Sitting Pulse Rate During the Extension Phase of the Study

Pulse rate was measured once for 30 seconds just prior to blood pressure measurements in the sitting position. (NCT00523744)
Timeframe: Baseline Phase 3 (Week 8) to end of Phase 3 (week 12)

InterventionBPM (beats per minute) (Mean)
Amlodipine+Valsartan+HCTZ - Phase 30.09

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Change in Sitting Pulse Rate During the Core Phase of the Study

Pulse rate was measured once for 30 seconds just prior to blood pressure measurements in the sitting position. (NCT00523744)
Timeframe: Baseline Phase 2 (Week 4) to end of Phase 2 (Week 8)

InterventionBPM (beats per minute) (Mean)
Amlodipine+Valsartan - Phase 2-1.93

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Change in Sitting Pulse Pressure During the Extension Phase of the Study

Pulse pressure is systolic pressure (SP) minus diastolic pressure (DP). The arm in which the highest sitting DPs were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, SP and DP were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00523744)
Timeframe: Baseline Phase 3 (Week 8) to end of Phase 3 (Week 12)

InterventionmmHg (Mean)
Amlodipine+Valsartan+HCTZ - Phase 3-5.62

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Change in Sitting Pulse Pressure During the Core Phase of the Study

Pulse pressure is systolic pressure (SP) minus diastolic pressure (DP). The arm in which the highest sitting DPs were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, SP and DP were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00523744)
Timeframe: Baseline Phase 2 (Week 4) to end of Phase 2 (Week 8)

InterventionmmHg (Mean)
Amlodipine+Valsartan - Phase 21.26

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Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Extension Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00523744)
Timeframe: Baseline Phase 3 (Week 8) to end of Phase 3 (Week 12)

InterventionmmHg (Mean)
Amlodipine+Valsartan+HCTZ - Phase 3-10.84

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Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Core Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00523744)
Timeframe: Baseline Phase 2 (Week 4) to end of Phase 2 (Week 8)

InterventionmmHg (Mean)
Amlodipine+Valsartan - Phase 2-7.87

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Extension Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00523744)
Timeframe: Baseline Phase 3 (Week 8) to end of Phase 3 (Week 12)

InterventionmmHg (Mean)
Amlodipine+Valsartan+HCTZ - Phase 3-5.22

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Core Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00523744)
Timeframe: Baseline Phase 2 (Week 4) to end of Phase 2 (Week 8)

InterventionmmHg (Mean)
Amlodipine+Valsartan - Phase 2-9.13

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"Number of Participants With Overall Fatal and Non-fatal, Major Adverse Cardiovascular Events (MACEs)"

number of MACEs in the two groups are reported. In addition, The primary endpoint was analyzed with event curves for the time-to-first event based on Kaplan-Meier analysis. Cox regression model was used to calculate hazard ratio (HR) and 95% Confidence Interval (CI). Due to the cluster randomized study design, a Cox shared-frailty model was fitted. multivariable model was adjusted for selected potential confounders: age, sex, systolic blood pressure (SBP), hemoglobin, estimated glomerular filtration rate (eGFR), albuminuria, HbA1c, total cholesterol and triglycerides (log-scaled) to reduce risk of bias. (NCT00535925)
Timeframe: 4 years (in the case the number of events needed by sample size is not reached at the expected 4-year time frame, primary end point will be assessed after the follow-up phase)

InterventionParticipants (Count of Participants)
Conventional Therapy146
Intensified Therapy116

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"Number of Participants Who Achieved of BP, HbA1c and Total, HDL and LDL Cholesterol Goals at the End of Intervention Phase"

Achievement of targets at end of intervention was performed applying generalized estimating equation (GEE) models, further adjusting for baseline values as covariate. (NCT00535925)
Timeframe: 13 years

InterventionParticipants (Count of Participants)
Standard of Care (SoC) Therapy150
Multifactorial Intensified Therapy191

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Change in Body Mass Index Between Baseline and 52 Week Assessments

Absolute change in Body Mass Index Baseline and 52 week assessments (NCT00546052)
Timeframe: 52 Weeks - Baseline

InterventionKg/m2 (Mean)
Losartan +/- Hydrochlorothiazide-7.3

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Absolute Change in C Reactive Protein Between Baseline and 52 Week Assessments

Absolute Change in C Reactive Protein Between Baseline and 52 week assessments: C Reactive Protein 52 weeks - C Reactive Protein Baseline. (NCT00546052)
Timeframe: 52 Weeks - Baseline

Interventionmg/L (Mean)
Losartan +/- Hydrochlorothiazide-0.36

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Absolute Change in Uric Acid Between Baseline and 52 Week Assessments

Absolute Change in Uric Acid Between Baseline and 52 week assessments: Uric Acid 52 weeks - Uric Acid Baseline. (NCT00546052)
Timeframe: 52 Weeks - Baseline

Interventionmmol/L (Mean)
Losartan +/- Hydrochlorothiazide-19.17

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Target Blood Pressure

Target Blood Pressure defined as Systolic Blood Pressure/Diastolic Blood Pressure ≤ 140/90 mm Hg at 52 weeks (NCT00546052)
Timeframe: 52 Weeks

,,
InterventionParticipants (Number)
Achieved Target Blood PressureDid NOT achieve target Blood Pressure
Overall Intend to Treat1200514
Overall Per Protocol1200311
Overall Total1200538

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Percent Change in Triglycerides Between Baseline and 52 Week Assessments

Percent Change in Triglycerides Between Baseline and 52 week assessments: 100% x [(Triglycerides 52 Weeks - Triglycerides Baseline) / (Triglycerides Baseline)]. (NCT00546052)
Timeframe: 52 Weeks - Baseline

InterventionPercent Change (Median)
Losartan +/- Hydrochlorothiazide1.09

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Percent Change in Total Cholesterol Between Baseline and 52 Week Assessments

Percent Change in Total Cholesterol Between Baseline and 52 week assessments: 100% x [(Total Cholesterol 52 weeks - Total Cholesterol Baseline) / (Total Cholesterol Baseline)]. (NCT00546052)
Timeframe: 52 Weeks - Baseline

InterventionPercent Change (Mean)
Losartan +/- Hydrochlorothiazide-2.98

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Percent Change in Low Density Lipoprotein-C Between Baseline and 52 Week Assessments

Percent Change in LDL-C Between Baseline and 52 week assessments: 100% x [(LDL-C 52 Weeks - LDL-C Baseline) / (LDL-C Baseline)]. (NCT00546052)
Timeframe: 52 Weeks - Baseline

InterventionPercent Change (Mean)
Losartan +/- Hydrochlorothiazide-1.49

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Percent Change in High Density Lipoprotein-C Between Baseline and 52 Week Assessments

Percent Change in HDL-C Between Baseline and 52 week assessments: 100% x [(HDL-C 52 Weeks - HDL-C 52 Baseline) / (HDL-C Baseline)]. (NCT00546052)
Timeframe: 52 Weeks - Baseline

InterventionPercent Change (Mean)
Losartan +/- Hydrochlorothiazide0.21

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Change in Waist Circumference Between Baseline and 52 Week Assessments

Absolute change in Waist Circumference between baseline and 52 week assessments (NCT00546052)
Timeframe: 52 Weeks - Baseline

Interventioncm (Mean)
Losartan +/- Hydrochlorothiazide-1.28

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Change in Systolic Blood Pressure Between Baseline and 52 Week Assessments

Absolute change in Systolic Blood Pressure between baseline and 52 week assessments. (NCT00546052)
Timeframe: 52 Weeks - Baseline

Interventionmm Hg (Mean)
Losartan +/- Hydrochlorothiazide-16.95

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Change in Hemoglobin A1c Between 52 Weeks and Baseline

Absolute Change in Hemoglobin A1c between 52 week measurement and baseline value. (NCT00546052)
Timeframe: 52 Weeks - Baseline

InterventionPercent (Median)
Losartan +/- Hydrochlorothiazide0.04

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Change in Fasting Blood Glucose Between Baseline and 52 Weeks Assessments

Absolute Change in Fasting Blood Glucose Measurements between Baseline and 52 week assessments. (NCT00546052)
Timeframe: 52 Weeks - Baseline

Interventionmmol/L (Mean)
Losartan +/- Hydrochlorothiazide0.02

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Change in Diastolic Blood Pressure Between Baseline and 52 Week Assessments

Absolute change in Diastolic Blood Pressure between baseline and 52 week assessments. (NCT00546052)
Timeframe: 52 Weeks - Baseline

Interventionmm Hg (Mean)
Losartan +/- Hydrochlorothiazide-9.84

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Number of Patients Achieving Target Blood Pressure at Week 6

Number of Patients Achieving Target Blood Pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics) at week 6 (NCT00546754)
Timeframe: Week 6

,
InterventionPatients (Number)
Achieved Target Blood PressureDid Not Achieve Target Blood Pressure
Losartan 50 mg/HCTZ 12.5 mg253140
Valsartan 80 mg/HCTZ 12.5 mg241104

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Change in Diastolic Blood Pressure From Baseline to Week 12

(NCT00546754)
Timeframe: Baseline and Week 12

Interventionmm Hg (Mean)
Losartan 50 mg/HCTZ 12.5 mg-10.6
Valsartan 80 mg/HCTZ 12.5 mg-10.5

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Change in Diastolic Blood Pressure From Baseline to Week 6

(NCT00546754)
Timeframe: Baseline and Week 6

Interventionmm Hg (Mean)
Losartan 50 mg/HCTZ 12.5 mg-8.4
Valsartan 80 mg/HCTZ 12.5 mg-9.1

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Change in Gamma-Glutamyl Transpeptidase (Gamma-GT) From Baseline to Week 12

(NCT00546754)
Timeframe: Baseline and Week 12

InterventionIU/L (Mean)
Losartan 50 mg/HCTZ 12.5 mg-0.7
Valsartan 80 mg/HCTZ 12.5 mg-0.0

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Change in Gamma-Glutamyl Transpeptidase (Gamma-GT) From Baseline to Week 6

(NCT00546754)
Timeframe: Baseline and Week 6

InterventionIU/L (Mean)
Losartan 50 mg/HCTZ 12.5 mg-1.8
Valsartan 80 mg/HCTZ 12.5 mg-0.1

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Change in Serum Highly Sensitive C-reactive Protein From Baseline to Week 12

(NCT00546754)
Timeframe: Baseline and Week 12

Interventionumol/L (Mean)
Losartan 50 mg/HCTZ 12.5 mg-0.3
Valsartan 80 mg/HCTZ 12.5 mg0.5

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Change in Serum Highly Sensitive C-reactive Protein From Baseline to Week 6

(NCT00546754)
Timeframe: Baseline and Week 6

Interventionmg/L (Mean)
Losartan 50 mg/HCTZ 12.5 mg0.8
Valsartan 80 mg/HCTZ 12.5 mg0.6

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Change in Systolic Blood Pressure From Baseline to Week 12

(NCT00546754)
Timeframe: Baseline and Week 12

Interventionmm Hg (Mean)
Losartan 50 mg/HCTZ 12.5 mg-19.9
Valsartan 80 mg/HCTZ 12.5 mg-20.8

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Change in Systolic Blood Pressure From Baseline to Week 6

(NCT00546754)
Timeframe: Baseline and Week 6

Interventionmm Hg (Mean)
Losartan 50 mg/HCTZ 12.5 mg-16.7
Valsartan 80 mg/HCTZ 12.5 mg-18.2

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Change in Uric Acid From Baseline to Week 12

(NCT00546754)
Timeframe: Baseline and Week 12

Interventionumol/L (Mean)
Losartan 50 mg/HCTZ 12.5 mg-0.4
Valsartan 80 mg/HCTZ 12.5 mg29.9

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Change in Uric Acid From Baseline to Week 6

(NCT00546754)
Timeframe: Baseline and Week 6

Interventionumol/L (Mean)
Losartan 50 mg/HCTZ 12.5 mg0.3
Valsartan 80 mg/HCTZ 12.5 mg21.7

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Time to Achieve Target Blood Pressure

Time to achieve the target blood pressure (<140/90 mmHg and <130/80 mmHg for diabetics) (NCT00546754)
Timeframe: 12 weeks

InterventionDays (Mean)
Losartan 50 mg/HCTZ 12.5 mg62.3
Valsartan 80 mg/HCTZ 12.5 mg57.3

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Number of Patients Achieving Target Blood Pressure at Week 12

Number of Patients Achieving Target Blood Pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics) at week 12 (NCT00546754)
Timeframe: 12 Weeks

,
InterventionPatients (Number)
Achieved Target Blood PressureDid Not Achieve Target Blood Pressure
Losartan 50 mg/HCTZ 12.5 mg27894
Valsartan 80 mg/HCTZ 12.5 mg25379

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Changes in Insulin Sensitivity

Measures of change in endogenous glucose production from baseline to final 30 minutes of clamp studies after 6 months of treatment. (NCT00574834)
Timeframe: 6 months

Interventionmg/kg/min (Mean)
Ramipril0.98
HCTZ1.5
Ramipril+HCTZ1.2

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Blood Pressure Outcome: Systolic BP

Blood pressure was measured as follows: the participant was in the sitting position, rested for 5 minutes, no caffeine or smoking 2 hours prior to measurement, using appropriate cuff size (covering 60% of upper arm length and 80% of arm circumference), correct cuff placement (1-2 inches above brachial pulse on bare arm), and the bell of the stethoscope. The systolic blood pressure was defined as the pressure corresponding to the first korotkoff sounds (K1) and the diastolic as the pressure corresponding to the last korotkoff sound (K5). Blood pressure was measured in both arms and recorded (NCT00605072)
Timeframe: Baseline-12 months

Interventionmm Hg (Least Squares Mean)
ACEI (Lisinopril)28
ARB (Candesartan)27
HCTZ21

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Cognitive Assessment: Forward Digit Span Test

This test consists of series of digits of increasing length, some of which are recited as presented, and some of which are to be recited in reversed order. The forward digit span score ranges from 0 (ie cannot repeat two digits) to 8 ( participant can repeat up to 8 digits) (NCT00605072)
Timeframe: Baseline-12 months

Interventionnumber of digits repeated (Least Squares Mean)
ACEI (Lisinopril)-0.3
ARB (Candesartan)0.02
HCTZ-0.04

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Cognitive Assessment: Trail Making Test Part B

This test requires the connection of sequentially numbered circles (A), and the connection of circles marked by numbers and letters in alternating sequence (B). This test is considered a benchmark of executive function. The test score is the time required to complete the task in seconds. (NCT00605072)
Timeframe: Baseline-12 months

Interventionseconds (Least Squares Mean)
ACEI (Lisinopril)-14
ARB (Candesartan)17
HCTZ4

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Cognitive Assessment: Hopkins Verbal Learning- Immediate Recall

This is a 12-item list learning test in which individuals are presented three learning and recall trials followed by a delayed recall and 24 item recognition test. The HVLT-R has been identified as an ideal memory measure for elderly patients, and appropriate reliability and validity have been shown in older individuals. The test score is the number of correct answers in the delayed recall ( score range 0-12) (NCT00605072)
Timeframe: Baseline-12 months

Interventionnumber words remembered (Least Squares Mean)
ACEI (Lisinopril)-1
ARB (Candesartan)-2
HCTZ-3

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Blood Flow Velocity, Sitting

This reports the change in the least square mean from baseline to 12 months, adjusted for age (NCT00605072)
Timeframe: Baseline-12 months

Interventioncm/sec (Least Squares Mean)
ACEI (Lisinopril)-0.3
ARB (Candesartan)-2.85
HCTZ0.35

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Plasma Potassium

Plasma potassium measured with indirect ion specific electrode method (NCT00605202)
Timeframe: Baseline and 2 weeks

,
Interventionmmol/l (Mean)
Baseline2 weeks
Licorice4.04.1
Licorice and HCTZ4.03.7

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Changes in Mean Sitting DBP From Baseline After 4 Weeks of Therapy

Mean of the changed DBP from baseline after 4 weeks (NCT00621153)
Timeframe: 4 weeks

InterventionmmHg (Least Squares Mean)
Candesartan Cilexetil/Hydroclorozide Combination Therapy-17.0
Candesartan Cilexetil Monotherapy-14.1

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Change in Mean 24-hour Ambulatory Blood Pressure From Baseline to Week 12 or Early Termination

(NCT00649389)
Timeframe: Baseline to 12 weeks or early termination

,,,
Interventionmm Hg (Mean)
Diastolic blood pressureSystolic blood pressure
AML10/HCTZ25-10.7-18.5
OM40/AML10-13.9-23.5
OM40/AML10/HCTZ25-18.0-30.3
OM40/HCTZ25-14.5-23.9

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Percentage of Subjects Who Reached Blood Pressure Goal (<140/90 mmHg; <130/80 mmHg for Subjects With Diabetes, Chronic Renal Disease, or Chronic Cardiovascular Disease)by 12 Weeks

(NCT00649389)
Timeframe: Baseline to 12 weeks

InterventionPercentage of subjects (Number)
OM40/AML1046.0
OM40/HCTZ2546.6
AML10/HCTZ2534.9
OM40/AML10/HCTZ2564.3

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Change in Seated Systolic Blood Pressure From Baseline to Week 12

(NCT00649389)
Timeframe: Baseline to week 12

Interventionmm Hg (Mean)
OM40/AML10-31.1
OM40/HCTZ25-31.2
AML10/HCTZ25-28.9
OM40/AML10/HCTZ25-38.1

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Change From Baseline to Week 12 in Seated Diastolic Blood Pressure (SeDBP).

(NCT00649389)
Timeframe: baseline to 12 weeks

Interventionmm Hg (Mean)
OM40/AML10-17.8
OM40/HCTZ25-16.5
AML10/HCTZ25-14.8
OM40/AML10/HCTZ25-21.5

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Number of Participants Achieving Mean Last 6 Hour Ambulatory Blood Pressure Thresholds at Week 12

number participants achieving mean last 6 hour ambulatory blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean last 6 hour BP < 135/85mean last 6 hour BP < 130/80mean last 6 hour BP < 125/75mean last 6 hour BP < 120/80mean last 6 hour SBP < 135mean last 6 hour SBP < 130mean last 6 hour SBP < 125mean last 6 hour SBP < 120mean last 6 hour DBP < 85mean last 6 hour DBP < 80mean last 6 hour DBP < 75
Aml + Olm + Hctz1351241018514312710885157146130

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Number of Participants Achieving Mean Last 4 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions

number of participants achieving mean last 4 hour ambulatory systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean last 4 hour SBP reduction =<15 mm Hgmean last 4 hour SBP reduction >15 & =<30 mm Hgmean last 4 hour SBP reduction >30 & =<45 mm Hgmean last 4 hour SBP reduction >45 mm Hgmean last 4 hour DBP reduction =<10 mm Hgmean last 4 hour DBP reduction >10 & =<15 mm Hgmean last 4 hour DBP reduction >15 & =<20 mm Hgmean last 4 hour DBP reduction >20 mm Hg
Aml + Olm + Hctz676528576362528

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Number of Participants Achieving Mean Last 4 Hour Ambulatory Blood Pressure Thresholds at Week 12

number of participants achieving mean last 4 hour ambulatory blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean last 4 hour BP < 135/85mean last 4 hour BP < 130/80mean last 4 hour BP < 125/75mean last 4 hour BP < 120/80mean last 4 hour SBP < 135mean last 4 hour SBP < 130mean last 4 hour SBP < 125mean last 4 hour SBP < 120mean last 4 hour DBP < 85mean last 4 hour DBP < 80mean last 4 hour DBP < 75
Aml + Olm + Hctz129107927213111410272150137120

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Number of Participants Achieving Mean Last 2 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12

number of participants achieving mean last 2 hour ambulatory systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean last 2 hour SBP reduction =<15 mm Hgmean last 2 hour SBP reduction >15 & =<30 mm Hgmean last 2 hour SBP reduction >30 & =<45 mm Hgmean last 2 hour SBP reduction >45 mm Hgmean last 2 hour DBP reduction =<10 mm Hgmean last 2 hour DBP reduction >10 & =<15 mm Hgmean last 2 hour DBP reduction >15 & =<20 mm Hgmean last 2 hour DBP reduction >20 mm Hg
Aml + Olm + Hctz636235577282931

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Number of Participants Achieving Mean Last 2 Hour Ambulatory Blood Pressure Thresholds at Week 12

number of participants achieving mean last 2 hour ambulatory blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean last 2 hour BP < 135/85mean last 2 hour BP < 130/80mean last 2 hour BP < 125/75mean last 2 hour BP < 120/80mean last 2 hour SBP < 135mean last 2 hour SBP < 130mean last 2 hour SBP < 125mean last 2 hour SBP < 120mean last 2 hour DBP < 85mean last 2 hour DBP < 80mean last 2 hour DBP < 75
Aml + Olm + Hctz11085634911592765114512594

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Number of Participants Achieving Mean Daytime Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12

number of participants achieving mean daytime ambulatory systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean daytime SBP reduction =<15 mm Hgmean daytime SBP reduction >15 & =<30 mm Hgmean daytime SBP reduction >30 & =<45 mm Hgmean daytime SBP reduction >45 mm Hgmean daytime DBP reduction =<10 mm Hgmean daytime DBP reduction >10 & =<15 mm Hgmean daytime DBP reduction >15 & =<20 mm Hgmean daytime DBP reduction >20 mm Hg
Aml + Olm + Hctz478431368413323

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Number of Participants Achieving Mean Daytime Ambulatory Blood Pressure Thresholds at Week 12

number of participants achieving mean daytime ambulatory blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean daytime BP < 135/85mean daytime BP < 130/80mean daytime BP < 125/75mean daytime BP < 120/80mean daytime SBP < 135mean daytime SBP < 130mean daytime SBP < 125mean daytime SBP < 120mean daytime DBP < 85mean daytime DBP < 80mean daytime DBP < 75
Aml + Olm + Hctz11683484211894674215112491

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Number of Participants Achieving Mean 24-hour Ambulatory Blood Pressure Thresholds at Week 12

number of participants achieving mean 24-hour ambulatory blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean 24-hour BP <135/85mean 24-hour BP <130/80mean 24-hour BP <125/75mean 24-hour BP <120/80mean 24-hour SBP <135mean 24-hour SBP <130mean 24-hour SBP <125mean 24-hour SBP <120mean 24-hour DBP <85mean 24-hour DBP <80mean 24-hour DBP <75
Aml + Olm + Hctz14011676591401209259158146121

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Number of Participants Achieving Mean 24 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12

number of participants achieving mean 24 hour ambulatory systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean 24-hour SBP reduction =<15 mm Hgmean 24-hour SBP reduction >15 & =<30 mm Hgmean 24-hour SBP reduction >30 & =<45 mm Hgmean 24-hour SBP reduction >45 mm Hgmean 24-hour DBP reduction =<10 mm Hgmean 24-hour DBP reduction >10 & =<15 mm Hgmean 24-hour DBP reduction >15 & =<20 mm Hgmean 24-hour DBP reduction >20 mm Hg
Aml + Olm + Hctz509122272473115

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Change in Mean Seated Systolic Blood Pressure (SeSBP) From Week 0 (Baseline) After 3, 6, 9, 12, 15, and 18 Weeks

change in mean SeSBP from week 0 (baseline) to Weeks 3, 6, 9, 12, 15, and 18. (NCT00654745)
Timeframe: week 0 - weeks 3, 6, 9, 12, 15, 18

Interventionmm Hg (Mean)
week 3 mean SBP change from baselineweek 6 mean SBP change from baselineweek 9 mean SBP change from baselineweek 12 mean SBP change from baselineweek 15 mean SBP change from baselineweek 18 mean SBP change from baseline
Aml + Olm + Hctz-10.3-17.9-20.0-23.7-28.5-31.1

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Change in Mean Seated Diastolic Blood Pressure (SeDBP) From Week 0 (Baseline) After 3, 6, 9, 12, 15, and 18 Weeks

change in mean SeDBP from week 0 (baseline) to Weeks 3, 6, 9, 12, 15, and 18. (NCT00654745)
Timeframe: week 0 - weeks 3, 6, 9, 12, 15, 18

Interventionmm Hg (Mean)
week 3 mean seDBP change from baselineweek 6 mean seDBP change from baselineweek 9 mean seDBP change from baselineweek 12 mean seDBP change from baselineweek 15 mean seDBP change from baselineweek 18 mean seDBP change from baseline
Aml + Olm + Hctz-4.1-8.2-9.7-11.2-14.4-15.1

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Change From Week 0 (Baseline) in Mean ABPM SBP After 12 Weeks of Active Treatment

Daytime mean SBP, Nighttime mean SBP, Last 6 hour mean SBP, Last 4 hour mean SBP, Last 2 hour mean SBP (NCT00654745)
Timeframe: week 0 - week 12 (24-hour, Daytime, Nighttime, Last 6 hour, Last 4 hour, Last 2 hour)

Interventionmm Hg (Mean)
daytime mean SBP change from baselinenighttime mean SBP change from baselinelast 6 hours mean SBP change from baselinelast 4 hours mean SBP change from baselinelast 2 hours mean SBP change from baseline
Aml + Olm + Hctz-20.8-18.5-18.9-19.1-19.5

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Change From Week 0 (Baseline) in Mean ABPM Diastolic Blood Pressure (DBP) After 12 Weeks of Active Treatment

24-hour mean DBP, Daytime mean DBP, Nighttime mean DBP, Last 6 hour mean DBP, Last 4 hour mean DBP, Last 2 hour mean DBP (NCT00654745)
Timeframe: week 0 - week 12 (24-hour, Daytime, Nighttime, Last 6 hour, Last 4 hour, Last 2 hour)

Interventionmm Hg (Mean)
24-hour mean DBP change from baselinedaytime mean DBP change from baselinenighttime mean DBP change from baselinelast 6 hour mean DBP change from baselinelast 4 hour mean DBP change from baselinelast 2 hour mean DBP change from baseline
Aml + Olm + Hctz-11.2-11.7-10.4-10.9-11.1-11.5

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Change From Week 0 (Baseline) in Mean 24-hour Ambulatory Blood Pressure Monitoring (ABPM) Systolic Blood Pressure (SBP) After 12 Weeks of Active Treatment

Change from week 0 (baseline) in mean 24-hour Ambulatory Blood Pressure Monitoring (ABPM) Systolic Blood Pressure (SBP) after 12 weeks of active treatment. change = week 12 - week 0. (NCT00654745)
Timeframe: week 0 - week 12

Interventionmm Hg (Mean)
Aml + Olm + Hctz-19.9

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Number of Participants Achieving Mean Nighttime Ambulatory Blood Pressure Thresholds at Week 12

number of participants achieving mean nighttime ambulatory blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, BP<120/70, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75, DBP<70 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean nighttime BP < 135/85mean nighttime BP < 130/80mean nighttime BP < 125/75mean nighttime BP < 120/80mean nighttime BP < 120/70mean nighttime SBP < 135mean nighttime SBP < 130mean nighttime SBP < 125mean nighttime SBP < 120mean nighttime DBP < 85mean nighttime DBP < 80mean nighttime DBP < 75mean nighttime DBP < 70
Aml + Olm + Hctz152137119112101154139123112160158147124

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Number of Participants Achieving Mean Nighttime Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12

number of participants achieving mean nighttime ambulatory systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean nighttime SBP reduction =<15 mm Hgmean nighttime SBP reduction >15 & =<30 mm Hgmean nighttime SBP reduction >30 & =<45 mm Hgmean nighttime SBP reduction >45 mm Hgmean nighttime DBP reduction =<10 mm Hgmean nighttime SBP reduction >10 & =<15 mm Hgmean nighttime SBP reduction >15 & =<20 mm Hgmean nighttime DBP reduction >20 mm Hg
Aml + Olm + Hctz607921580412123

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Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 12

number of participants achieving mean seated systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean seated SBP reduction =<15 mm Hgmean seated SBP reduction >15 & =<30 mm Hgmean seated SBP reduction >30 & =<45 mm Hgmean seated SBP reduction >45 mm Hgmean seated DBP reduction =<10 mm Hgmean seated DBP reduction >10 & =<15 mm Hgmean seated DBP reduction >15 & =<20 mm Hgmean seated DBP reduction >20 mm Hg
Aml + Olm + Hctz4873451185422723

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Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 15

number of participants achieving mean seated systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 15 (NCT00654745)
Timeframe: week 0 - week 15

Interventionparticipants (Number)
mean seated SBP reduction =<15 mm Hgmean seated SBP reduction >15 & =<30 mm Hgmean seated SBP reduction >30 & =<45 mm Hgmean seated SBP reduction >45 mm Hgmean seated DBP reduction =<10 mm Hgmean seated DBP reduction >10 & =<15 mm Hgmean seated DBP reduction >15 & =<20 mm Hgmean seated DBP reduction >20 mm Hg
Aml + Olm + Hctz3166552052453243

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Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 18

number of participants achieving mean seated systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 18 (NCT00654745)
Timeframe: week 0 - week 18

Interventionparticipants (Number)
mean seated SBP reduction =<15 mm Hgmean seated SBP reduction >15 & =<30 mm Hgmean seated SBP reduction >30 & =<45 mm Hgmean seated SBP reduction >45 mm Hgmean seated DBP reduction =<10 mm Hgmean seated DBP reduction >10 & =<15 mm Hgmean seated DBP reduction >15 & =<20 mm Hgmean seated DBP reduction >20 mm Hg
Aml + Olm + Hctz2253642550332952

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Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 3

number of participants achieving mean seated systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 3 (NCT00654745)
Timeframe: week 0 - week 3

Interventionparticipants (Number)
mean seated SBP reduction =<15 mm Hgmean seated SBP reduction >15 & =<30 mm Hgmean seated SBP reduction >30 & =<45 mm Hgmean seated SBP reduction >45 mm Hgmean seated DBP reduction =<10 mm Hgmean seated DBP reduction >10 & =<15 mm Hgmean seated DBP reduction >15 & =<20 mm Hgmean seated DBP reduction >20 mm Hg
Aml + Olm + Hctz131626216325103

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Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 6

number of participants achieving mean seated systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 6 (NCT00654745)
Timeframe: week 0 - week 6

Interventionparticipants (Number)
mean seated SBP reduction =<15 mm Hgmean seated SBP reduction >15 & =<30 mm Hgmean seated SBP reduction >30 & =<45 mm Hgmean seated SBP reduction >45 mm Hgmean seated DBP reduction =<10 mm Hgmean seated DBP reduction >10 & =<15 mm Hgmean seated DBP reduction >15 & =<20 mm Hgmean seated DBP reduction >20 mm Hg
Aml + Olm + Hctz6990312120332415

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Number of Participants Achieving Mean Seated Systolic and Diastolic Blood Pressure Reductions at Week 9

number of participants achieving mean seated systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 9 (NCT00654745)
Timeframe: week 0 - week 9

Interventionparticipants (Number)
mean seated SBP reduction =<15 mm Hgmean seated SBP reduction >15 & =<30 mm Hgmean seated SBP reduction >30 & =<45 mm Hgmean seated SBP reduction >45 mm Hgmean seated DBP reduction =<10 mm Hgmean seated DBP reduction >10 & =<15 mm Hgmean seated DBP reduction >15 & =<20 mm Hgmean seated DBP reduction >20 mm Hg
Aml + Olm + Hctz7269349100431823

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Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 12

number of participants achieving seated systolic and diastolic blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean BP < 135/85mean BP < 130/80mean BP < 125/75mean BP < 120/80mean SBP < 135mean SBP < 130mean SBP < 125mean SBP < 120mean DBP < 85mean DBP < 80mean DBP < 75
Aml + Olm + Hctz866133289370462813410574

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Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 15

number of participants achieving seated systolic and diastolic blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 15 (NCT00654745)
Timeframe: week 0 - week 15

Interventionparticipants (Number)
mean BP < 135/85mean BP < 130/80mean BP < 125/75mean BP < 120/80mean SBP < 135mean SBP < 130mean SBP < 125mean SBP < 120mean DBP < 85mean DBP < 80mean DBP < 75
Aml + Olm + Hctz11483514511695694815312296

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Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 18

number of participants achieving seated systolic and diastolic blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 18 (NCT00654745)
Timeframe: week 0 - week 18

Interventionparticipants (Number)
mean BP < 135/85mean BP < 130/80mean BP < 125/75mean BP < 120/80mean SBP < 135mean SBP < 130mean SBP < 125mean SBP < 120mean DBP < 85mean DBP < 80mean DBP < 75
Aml + Olm + Hctz117875649123101745114712894

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Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 3

number of participants achieving seated systolic and diastolic blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 3 (NCT00654745)
Timeframe: week 0 - week 3

Interventionparticipants (Number)
mean BP < 135/85mean BP < 130/80mean BP < 125/75mean BP < 120/80mean SBP < 135mean SBP < 130mean SBP < 125mean SBP < 120mean DBP < 85mean DBP < 80mean DBP < 75
Aml + Olm + Hctz311042411792995829

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Number of Participants Achieving Mean Last 6 Hour Ambulatory Systolic and Diastolic Blood Pressure Reductions at Week 12

number of participants achieving mean last 6 hour ambulatory systolic and diastolic blood pressure reductions of; SBP reduction <= 15 mmHg, SBP reduction > 15 mmHg & <= 30 mmHg, SBP reduction > 30 mmHg & <= 45 mmHg, SBP reduction > 45 mmHg, DBP reduction <= 10 mmHg, DBP reduction > 10 mmHg & <= 15 mmHg, DBP reduction > 15 mmHg & <= 20 mmHg, DBP reduction > 20 mmHg at week 12 (NCT00654745)
Timeframe: week 0 - week 12

Interventionparticipants (Number)
mean last 6 hour SBP reduction =<15 mm Hgmean last 6 hour SBP reduction >15 & =<30 mm Hgmean last 6 hour SBP reduction >30 & =<45 mm Hgmean last 6 hour SBP reduction >45 mm Hgmean last 6 hour DBP reduction =<10 mm Hgmean last 6 hour DBP reduction >10 & =<15 mm Hgmean last 6 hour DBP reduction >15 & =<20 mm Hgmean last 6 hour DBP reduction >20 mm Hg
Aml + Olm + Hctz617623576412721

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Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 6

number of participants achieving seated systolic and diastolic blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 6 (NCT00654745)
Timeframe: week 0 - week 6

Interventionparticipants (Number)
mean BP < 135/85mean BP < 130/80mean BP < 125/75mean BP < 120/80mean SBP < 135mean SBP < 130mean SBP < 125mean SBP < 120mean DBP < 85mean DBP < 80mean DBP < 75
Aml + Olm + Hctz61361813734831141279148

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Number of Participants Achieving Seated Systolic and Diastolic Blood Pressure Thresholds at Week 9

number of participants achieving seated systolic and diastolic blood pressure thresholds BP<135/85, BP<130/80, BP<125/75, BP<120/80, SBP<135, SBP<130, SBP<125, SBP<120, DBP<85, DBP<80, DBP<75 at week 9 (NCT00654745)
Timeframe: week 0 - week 9

Interventionparticipants (Number)
mean BP < 135/85mean BP < 130/80mean BP < 125/75mean BP < 120/80mean SBP < 135mean SBP < 130mean SBP < 125mean SBP < 120mean DBP < 85mean DBP < 80mean DBP < 75
Aml + Olm + Hctz76472519826141201329564

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Percentage of Subjects Achieving Blood Pressure Goals

Percentage of subjects who achieved JNC-VII defined blood pressure goals. (NCT00661895)
Timeframe: 3 month intervals

Interventionpercentage of participants (Number)
Intervention81
Control57

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Percentage of Participants Who Achieved a Blood Pressure Response in Mean Sitting Systolic Blood Pressure

Systolic blood pressure response was defined as a mean sitting systolic blood pressure <140 mmHg or a >=20 mmHg reduction from baseline value. Week 28 Endpoint was the last non-missing post-baseline measurement value on or before Week 28, and Week 54 Endpoint was the last non-missing measurement value after Week 28. (NCT00667719)
Timeframe: Weeks 28 and 54 endpoints

Interventionpercentage of participants (Number)
Week 28 EndpointWeek 54 Endpoint
Aliskiren/Amlodipine/Hydrochlorothiazide90.293.7

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the participant in a sitting position for five minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. Week 28 Endpoint was the last non-missing post-baseline measurement value on or before Week 28, and Week 54 Endpoint was the last non-missing measurement value after Week 28. (NCT00667719)
Timeframe: Baseline, Weeks 28 and 54 endpoints

Interventionmillimeters of mercury (Mean)
BaselineChange from baseline to Week 28 EndpointChange from Baseline to Week 54 Endpoint
Aliskiren/Amlodipine/Hydrochlorothiazide166.1-34.2-37.3

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Number of Participants With Any Adverse Events (AEs), Serious Adverse Events (SAEs) and Death

An AE was defined as the appearance or worsening of any undesirable sign, symptom, or medical condition occurring after starting the study drug, even if the event is not considered to be related to study drug. An SAE was defined as an event which was fatal or life-threatening, resulted in persistent or significant disability/incapacity, constituted a congenital anomaly/birth defect, required inpatient hospitalization or prolongation of existing hospitalization, was medically significant, i.e. defined as an event that jeopardizes the participant or may require medical or surgical intervention to prevent one of the outcomes listed above. (NCT00667719)
Timeframe: 54 weeks

,,
InterventionParticipants (Count of Participants)
Any Adverse EventsSerious Adverse EventsDeath
Aliskiren/Amlodipine/Hydrochlorothiazide 300/10/25 mg255140
Aliskiren/Amlodipine/Hydrochlorothiazide 300/5/12.5 mg5410
Aliskiren/Hydrochlorothiazide 300/12.5 mg5700

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Percentage of Participants Achieving the Blood Pressure Control Target of <140/90 mmHg

Blood pressure control was defined as having a mean sitting diastolic blood pressure <90 mmHg and a mean sitting systolic blood pressure <140 mmHg. Percentage of participants achieving the blood pressure control of < 140/90 mmHg were reported. Week 28 Endpoint was the last non-missing post-baseline measurement value on or before Week 28 and Week 54 Endpoint was the last non-missing measurement value after Week 28. (NCT00667719)
Timeframe: Weeks 28 and 54 endpoints

Interventionpercentage of participants (Number)
Week 28 EndpointWeek 54 Endpoint
Aliskiren/Amlodipine/Hydrochlorothiazide69.177.1

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the participant in a sitting position for five minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. Week 28 Endpoint was the last non-missing post-baseline measurement value on or before Week 28, and Week 54 Endpoint was the last non-missing measurement value after Week 28. (NCT00667719)
Timeframe: Baseline, Weeks 28 and 54 endpoint

InterventionmmHg (Mean)
BaselineChange from Baseline to Week 28 EndpointChange from Baseline to Week 54 Endpoint
Aliskiren/Amlodipine/Hydrochlorothiazide101.8-20.3-21.8

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Percentage of Participants Who Achieved a Blood Pressure Response in Mean Sitting Diastolic Blood Pressure

Diastolic Blood pressure response was defined as a mean sitting diastolic blood pressure <90 mmHg or a >=10 mmHg reduction from baseline value. Week 28 Endpoint was the last non-missing post-baseline measurement value on or before Week 28, and Week 54 Endpoint was the last non-missing measurement value after Week 28. (NCT00667719)
Timeframe: Weeks 28 and 54 endpoints

Interventionpercentage of participants (Number)
Week 28 EndpointWeek 54 Endpoint
Aliskiren/Amlodipine/Hydrochlorothiazide91.896.6

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Change From Baseline in Sitting Clinic Systolic Blood Pressure - Cohort 2

The change between sitting clinic systolic blood pressure measured at each week assessed relative to the baseline measurement. Mean calculated by using the average (arithmetic mean) of 3 measurements performed at each visit. (NCT00695955)
Timeframe: 52 weeks

InterventionmmHg (Mean)
Week 4Week 8Week 12Week 16Week 26Week 36Week 46Week 56Final Visit
Cohort 2-14.4-17.5-23.8-26.2-24.8-22.5-23.8-24.2-22.7

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Change From Baseline in Sitting Clinic Diastolic Blood Pressure - Cohort 1.

The change between sitting clinic diastolic blood pressure measured at each week assessed relative to the baseline measurement. Mean calculated by using the average (arithmetic mean) of 3 measurements performed at each visit. (NCT00695955)
Timeframe: 52 weeks.

InterventionmmHg (Mean)
Week 4Week 8Week 12Week 16Week 26Week 36Week 46Week 56Final Visit
Cohort 1-8.9-11.0-15.9-18.7-18.6-19.9-19.8-18.4-16.5

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Change From Baseline in Sitting Clinic Diastolic Blood Pressure - Cohort 2.

The change between sitting clinic diastolic blood pressure measured at each week assessed relative to the baseline measurement. Mean calculated by using the average (arithmetic mean) of 3 measurements performed at each visit. (NCT00695955)
Timeframe: 52 weeks.

InterventionmmHg (Mean)
Week 4Week 8Week 12Week 16Week 26Week 36Week 46Week 56Final Visit
Cohort 2-10.6-12.3-16.8-18.2-17.7-16.2-17.2-17.9-16.2

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Change From Baseline in Sitting Clinic Systolic Blood Pressure - Cohort 1.

The change between sitting clinic systolic blood pressure measured at each week assessed relative to the baseline measurement. Mean calculated by using the average (arithmetic mean) of 3 measurements performed at each visit. (NCT00695955)
Timeframe: 52 weeks

InterventionmmHg (Mean)
Week 4Week 8Week 12Week 16Week 26Week 36Week 46Week 56Final Visit
Cohort 1-10.1-13.1-21.5-25.4-26.3-27.3-28.1-25.2-22.1

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Number of Participants Reporting One or More Treatment-emergent Adverse Events From Day 1 Through End of the Study - Cohort 1.

Treatment-emergent adverse events are defined as any unfavorable and unintended sign, symptom or disease temporally associated with the use of a medicinal product reported from first dose of study drug through 14 days after the last dose of study drug, or if a serious adverse event, within 30 days after the last dose of study drug. (NCT00695955)
Timeframe: 56 weeks.

Interventionparticipants (Number)
Number of ParticipantsPercentage of Participants
Cohort 126773.8

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Number of Participants Reporting One or More Treatment-emergent Adverse Events From Day 1 Through End of the Study - Cohort 2.

Treatment-emergent adverse events are defined as any unfavorable and unintended sign, symptom or disease temporally associated with the use of a medicinal product reported from first dose of study drug through 14 days after the last dose of study drug, or if a serious adverse event, within 30 days after the last dose of study drug. (NCT00695955)
Timeframe: 56 weeks.

Interventionparticipants (Number)
Number of ParticipantsPercentage of Participants
Cohort 224178.5

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Change From Baseline to Week 4 in Office Cuff Mean Sitting Systolic Blood Pressure (MSSBP)

(NCT00698646)
Timeframe: Baseline and Week 4

,,
Interventionmm Hg (Mean)
BaselineWeek 4Change in MSSBP from Baseline to Week 4
HCTZ164.5150.9-13.6
Valsartan166.2157.5-8.6
Valsartan + HCTZ164.5147.1-17.3

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Cumulative Percentage of Patients Achieving the Blood Pressure Control of < 140/90 mmHg

Cumulative refers to achieving of blood pressure control before or at the corresponding visit. (NCT00698646)
Timeframe: Weeks 4, 8, 12 and 16

,,
InterventionPercentage of Participants (Number)
Week 4Week 8Week 12Week 16
HCTZ37.350.7961.1166.67
Valsartan2540.635055.47
Valsartan + HCTZ49.2163.4969.0572.22

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Cumulative Percentage of Patients Achieving Blood Pressure Goal (MSSBP < 140 mmHg)

Cumulative refers to achieving blood pressure goal before or at the corresponding visit. (NCT00698646)
Timeframe: Weeks 4, 8, 12 and 16

,,
InterventionPercentage of Participants (Number)
Week 4Week 8Week 12Week 16
HCTZ38.8952.3862.7068.25
Valsartan2540.635056.25
Valsartan + HCTZ49.2163.4969.0572.22

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Change From Baseline to Weeks 8, 12 and 16 in Office Cuff Mean Sitting Systolic Blood Pressure (MSSBP)

(NCT00698646)
Timeframe: Baseline and Weeks 8, 12, and 16

,,
Interventionmm Hg (Mean)
BaselineWeek 8Change in MSSBP from Baseline to Week 8Week 12Change in MSSBP from Baseline to Week 12Week 16Change in MSSBP from Baseline to Week 16
HCTZ164.5147.4-17.1145.1-19.4144.9-19.7
Valsartan166.2150.4-15.7148.6-17.5148.7-17.5
Valsartan + HCTZ164.5144.2-20.2142.0-22.5143.5-20.9

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Change From Baseline to Week 4, 8, 12 and 16 in Office Cuff Mean Sitting Diastolic Blood Pressure (MSDBP)

(NCT00698646)
Timeframe: Baseline and Weeks 4, 8, 12 and 16

,,
Interventionmm Hg (Mean)
BaselineWeek 4Change in MSDBP from Baseline to Week 4Week 8Change in MSDBP from Baseline to Week 8Week 12Change in MSDBP from Baseline to Week 12Week 16Change in MSDBP from Baseline to Week 16
HCTZ85.581.6-3.979.1-6.478.1-7.377.9-7.5
Valsartan84.981.0-3.978.3-6.677.6-7.377.8-7.1
Valsartan + HCTZ84.877.8-7.176.5-8.475.4-9.576.6-8.3

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Time in Weeks to Achieving the First Treatment Success (Defined as the Time of the First Achievement of the Target Blood Pressure Goal [MSSBP/MSDBP <140/90 mmHg])

(NCT00698646)
Timeframe: During 16 weeks

InterventionWeeks (Median)
Valsartan12.0
HCTZ8.0
Valsartan + HCTZ4.0

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Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to End of Study (Week 12)

At the first visit, blood pressure (BP) was measured in both arms and the arm having the higher BP reading was the arm used for all subsequent readings throughout the study. Patients were required to sit for five minutes with feet flat on the floor, with arm resting so that the bottom of the cuff was at the same level as the heart. BP was measured three times at 1 to 2-minute intervals at each visit using the correct cuff size. The mean BP was calculated from the 3 readings. (NCT00705575)
Timeframe: Baseline to end of study (Week 12)

Interventionmm Hg (Least Squares Mean)
Aliskiren/Hydrochlorothiazide (HCTZ) (300/25 mg)-30.01
Aliskiren (300 mg)-20.29

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Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to Week 8

At the first visit, blood pressure (BP) was measured in both arms and the arm having the higher BP reading was the arm used for all subsequent readings throughout the study. Patients were required to sit for five minutes with feet flat on the floor, with arm resting so that the bottom of the cuff was at the same level as the heart. BP was measured three times at 1 to 2-minute intervals at each visit using the correct cuff size. The mean BP was calculated from the 3 readings. (NCT00705575)
Timeframe: Baseline to Week 8

Interventionmm Hg (Least Squares Mean)
Aliskiren/Hydrochlorothiazide (HCTZ) (300/25 mg)-30.09
Aliskiren (300 mg)-20.75

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Percentage of Patients Achieving the Target Blood Pressure (msSBP < 140 mm Hg and msDBP < 90 mm Hg, and msSBP < 130 mm Hg and msDBP < 80 mm Hg for Diabetics) at Week 8 and Week 12

At the first visit, blood pressure (BP) was measured in both arms and the arm having the higher BP reading was the arm used for all subsequent readings throughout the study. Patients were required to sit for five minutes with feet flat on the floor, with arm resting so that the bottom of the cuff was at the same level as the heart. BP was measured three times at 1 to 2-minute intervals at each visit using the correct cuff size. The mean BP was calculated from the 3 readings. (NCT00705575)
Timeframe: Baseline to Week 12

,
InterventionPercentage (Number)
Baseline to Week 8Baseline to Week 12
Aliskiren (300 mg)30.432.2
Aliskiren/Hydrochlorothiazide (HCTZ) (300/25 mg)53.554.6

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) From Baseline to Week 8 and to Week 12

At the first visit, blood pressure (BP) was measured in both arms and the arm having the higher BP reading was the arm used for all subsequent readings throughout the study. Patients were required to sit for five minutes with feet flat on the floor, with arm resting so that the bottom of the cuff was at the same level as the heart. BP was measured three times at 1 to 2-minute intervals at each visit using the correct cuff size. The mean BP was calculated from the 3 readings. (NCT00705575)
Timeframe: Baseline to Week 12

,
Interventionmm Hg (Least Squares Mean)
Baseline to Week 8Baseline to Week 12
Aliskiren (300 mg)-7.99-8.18
Aliskiren/Hydrochlorothiazide (HCTZ) (300/25 mg)-13.69-12.64

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Percentage of Responders After 8 Weeks of Treatment.

To compare the percentage of responders after 8 weeks of treatment with an aliskiren HCTZ based treatment regimen (aliskiren HCTZ 150/12.5 mg, 300/25 mg) versus an amlodipine-based treatment regimen (amlodipine 5 mg, 10 mg) in African American patients with stage 2 hypertension: [ Responders were defined as patients with MSSBP < 140 mm Hg or a decrease from baseline ≥ 20 mm Hg at 1st response. A response was counted when a patient first achieved MSSBP < 140 mm Hg or a decrease from baseline ≥ 20 mm Hg.] (NCT00739596)
Timeframe: 8 weeks

InterventionCumulative percentage of responders (Number)
Aliskiren HCTZ84.6
Amlodipine90.7

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Percentage of Participants Achieving BP Control After 8 Weeks of Treatment

To compare the percentage of patients achieving BP control (<140/90 mm Hg) after 8 weeks of treatment with an aliskiren HCTZ-based treatment regimen (aliskiren HCTZ 150/12.5 mg, 300/25 mg) versus an amlodipine-based treatment regimen (amlodipine 5 mg, 10 mg) in African American patients with stage 2 hypertension. (NCT00739596)
Timeframe: 8 weeks

InterventionCumulative percentage of participants (Number)
Aliskiren HCTZ63.6
Amlodipine62.3

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Change in Mean Sitting Diastolic Blood Pressure (MSDBP) After 8 Weeks of Treatment

To assess the change from baseline in mean sitting diastolic blood pressure (MSDBP) after 8 weeks of treatment with an aliskiren HCTZ-based treatment regimen (aliskiren HCTZ 150/12.5 mg, 300/25 mg) versus an amlodipine-based treatment regimen (amlodipine 5 mg, 10 mg) in African American patients with stage 2 hypertension. (NCT00739596)
Timeframe: Baseline and 8 weeks

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from Baseline to Week 8
Aliskiren HCTZ96.086.0-10.0
Amlodipine95.084.0-11.0

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Change in Mean Sitting Systolic Blood Pressure (MSSBP) After 8 Weeks of Treatment

To assess the change from baseline in MSSBP after 8 weeks of treatment with an aliskiren HCTZ-based treatment regimen (aliskiren HCTZ 150/12.5 mg, 300/25 mg) versus an amlodipine-based treatment regimen (amlodipine 5 mg, 10 mg) in African American patients with stage 2 hypertension. (NCT00739596)
Timeframe: Baseline and 8 weeks

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from baseline to Week 8
Aliskiren HCTZ168.2138.8-29.4
Amlodipine168.1139.1-29.0

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Change in Mean Sitting Pulse Pressure (MSPP) After 8 Weeks of Treatment

To compare the change from baseline in mean sitting pulse pressure (MSPP) after 8 weeks of treatment with an aliskiren HCTZ-based treatment regimen (aliskiren HCTZ 150/12.5 mg, 300/25 mg) versus an amlodipine-based treatment regimen (amlodipine 5 mg, 10 mg) in African American patients with stage 2 hypertension. (NCT00739596)
Timeframe: Baseline and 8 weeks

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from Baseline to Week 8
Aliskiren HCTZ72.252.7-19.4
Amlodipine73.155.1-18.0

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Change in Diastolic Blood Pressure From Baseline to Week 6

(NCT00739674)
Timeframe: 6 Weeks

Interventionmm Hg (Mean)
Losartan-Based Regimen Alone (L Group)-8.34
Diet Management and Losartan-Based Regimen (DML Group)-9.76

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Change in Diastolic Blood Pressure From Baseline to Week 14

(NCT00739674)
Timeframe: 14 Weeks

Interventionmm Hg (Mean)
Losartan-Based Regimen Alone (L Group)-10.19
Diet Management and Losartan-Based Regimen (DML Group)-12.05

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Change in Diastolic Blood Pressure From Baseline to Week 10

(NCT00739674)
Timeframe: 10 Weeks

Interventionmm Hg (Mean)
Losartan-Based Regimen Alone (L Group)-9.48
Diet Management and Losartan-Based Regimen (DML Group)-11.42

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Number of Patients Achieving Target Blood Pressure at Week 6 From Baseline

Number of Patients Achieving Target Blood Pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics) from baseline after 6 weeks of treatment (NCT00739674)
Timeframe: 6 Weeks

,
InterventionParticipants (Number)
Achieve Target Blood PressureDid not Achieve Target Blood Pressure
Diet Management and Losartan-Based Regimen (DML Group)231152
Losartan-Based Regimen Alone (L Group)239192

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Number of Patients Achieving Target Blood Pressure at Week 40 From Baseline

Number of Patients Achieving Target Blood Pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics) from baseline after 40 weeks of treatment (NCT00739674)
Timeframe: 40 Weeks

,
InterventionParticipants (Number)
Achieve Target Blood PressureDid not Achieve Target Blood Pressure
Diet Management and Losartan-Based Regimen (DML Group)24091
Losartan-Based Regimen Alone (L Group)26487

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Number of Patients Achieving Target Blood Pressure at Week 14 From Baseline

Number of Patients Achieving Target Blood Pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics) from baseline after 14 weeks of treatment (NCT00739674)
Timeframe: 14 Weeks

,
InterventionParticipants (Number)
Achieve Target Blood PressureDid not Achieve Target Blood Pressure
Diet Management and Losartan-Based Regimen (DML Group)27087
Losartan-Based Regimen Alone (L Group)276116

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Time to Achieve the Target Blood Pressure From Baseline

Time to achieve the target blood pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics). (NCT00739674)
Timeframe: 14 Weeks

InterventionWeeks (Median)
Losartan-Based Regimen Alone (L Group)7.43
Diet Management and Losartan-Based Regimen (DML Group)6.57

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Change in Systolic Blood Pressure From Baseline to Week 6

(NCT00739674)
Timeframe: 6 Weeks

Interventionmm Hg (Mean)
Losartan-Based Regimen Alone (L Group)-16.81
Diet Management and Losartan-Based Regimen (DML Group)-18.85

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Change in Systolic Blood Pressure From Baseline to Week 14

(NCT00739674)
Timeframe: 14 Weeks

Interventionmm Hg (Mean)
Losartan-Based Regimen Alone (L Group)-21.01
Diet Management and Losartan-Based Regimen (DML Group)-22.74

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Change in Systolic Blood Pressure From Baseline to Week 10

(NCT00739674)
Timeframe: 10 Weeks

Interventionmm Hg (Mean)
Losartan-Based Regimen Alone (L Group)-19.11
Diet Management and Losartan-Based Regimen (DML Group)-20.95

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Number of Patients Achieving Target Blood Pressure at Week 10 From Baseline

Number of Patients Achieving Target Blood Pressure (<140/90 mm Hg and <130/80 mm Hg for diabetics) from baseline after 10 weeks of treatment (NCT00739674)
Timeframe: 10 Weeks

,
InterventionParticipants (Number)
Achieve Target Blood PressureDid not Achieve Target Blood Pressure
Diet Management and Losartan-Based Regimen (DML Group)254116
Losartan-Based Regimen Alone (L Group)257142

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Percentage of Subjects Achieving Blood Pressure Control at Weeks 4 and 8

Blood pressure control defined as mean sitting Systolic Blood Pressure < 140 mm Hg and mean sitting Diastolic Blood Pressure < 90 mm Hg (NCT00760266)
Timeframe: At Weeks 4 and 8

,
InterventionPercentage of Participants (Number)
week 4week 8
Aliskiren/HCTZ49.862.2
HCTZ33.339.2

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Percentage of Responders at Week 4 and Week 8

Responders defined as mean sitting Systolic Blood Pressure < 140 mmHg or reduction of ≥ 20 mmHg from baseline (NCT00760266)
Timeframe: At 4 weeks and 8 weeks

,
InterventionPercentage of Participants (Number)
Week 4Week 8
Aliskiren/HCTZ73.383.1
HCTZ55.967.6

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Change in Mean Sitting Systolic Blood Pressure (msSBP) and Mean Sitting Diastolic Blood Pressure (msDBP) (in Patients With msDBP ≥90 mmHg at Baseline) From Baseline to Week 8

(NCT00760266)
Timeframe: Baseline and Week 8

,
Interventionmm Hg (Least Squares Mean)
msSBPmsDBP (N = 130 , 133)
Aliskiren/HCTZ-33.2-13.3
HCTZ-25.7-10.1

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Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to Week 4

(NCT00760266)
Timeframe: Baseline and Week 4

Interventionmm Hg (Least Squares Mean)
Aliskiren/HCTZ-29.6
HCTZ-22.3

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) From Baseline to Week 4

(NCT00760266)
Timeframe: Baseline and Week 4

Interventionmm Hg (Least Squares Mean)
Aliskiren/HCTZ-11.1
HCTZ-9.2

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Change in Mean 24-hour Ambulatory Systolic and Diastolic Blood Pressure From Baseline to End of Study (Week 8)

Twenty-four hour ambulatory blood pressure monitoring (ABPM) was performed in a subset of patients twice during the study, once at baseline and again at Week 8. The ABPM device was placed on the non-dominant arm between 7:00 and 10:00 am and verification readings obtained. If they were successful, the investigator initiated the 24 hour reading and instructed the patient regarding ABPM procedures. On the next day, the ABPM device was removed if it had been worn for a minimum of 24 hours. The ABPM data were downloaded and evaluated on site. (NCT00765674)
Timeframe: Baseline to end of study (Week 8)

,,,
InterventionmmHg (Least Squares Mean)
Systolic BPDiastolic BP
Aliskiren / Amlodipine-20.30-13.29
Aliskiren / Amlodipine / Hydrochlorothiazide-25.29-15.90
Aliskiren / Hydrochlorothiazide-16.27-9.57
Amlodipine / Hydrochlorothiazide-18.67-11.20

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Percentage of Patients Achieving Blood Pressure Control at the End of the Study (Week 8)

Blood pressure control was defined as a msSBP/msDBP < 140/90 mmHg at the end of the study (Week 8). Blood pressure (BP) was measured at trough (24±3 hours post-dose). The arm in which the highest sitting diastolic BP was found at study entry was used for all subsequent readings. At each visit, after the patient was in a sitting position with the back supported and both feet placed on the floor for 5 minutes, systolic and diastolic BP were measured 3 times with an automated BP monitor and appropriate size cuff. Means of the 3 measurements were calculated. (NCT00765674)
Timeframe: End of study (Week 8)

InterventionPercentage of patients (Number)
Aliskiren / Amlodipine41.3
Aliskiren / Hydrochlorothiazide33.1
Amlodipine / Hydrochlorothiazide39.0
Aliskiren / Amlodipine / Hydrochlorothiazide62.3

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) From Baseline to End of Study (Week 8)

Blood pressure (BP) was measured at trough (24±3 hours post-dose). The arm in which the highest sitting diastolic BP was found at study entry was used for all subsequent readings. If there was < 0.5 mmHg difference in BP between the 2 arms, the non-dominant arm was used. At each visit, after the patient was in a sitting position with the back supported and both feet placed on the floor for 5 minutes, systolic and diastolic BP were measured 3 times with an automated BP monitor and appropriate size cuff. Means of the 3 measurements were calculated. A negative change indicates lowered BP. (NCT00765674)
Timeframe: Baseline to end of study (Week 8)

InterventionmmHg (Least Squares Mean)
Aliskiren / Amlodipine-18.03
Aliskiren / Hydrochlorothiazide-14.32
Amlodipine / Hydrochlorothiazide-17.03
Aliskiren / Amlodipine / Hydrochlorothiazide-20.63

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Change in Mean Sitting Systolic Blood Pressure (msSBP) From Baseline to End of Study (Week 8)

Blood pressure (BP) was measured at trough (24±3 hours post-dose). The arm in which the highest sitting diastolic BP was found at study entry was used for all subsequent readings. If there was < 0.5 mmHg difference in BP between the 2 arms, the non-dominant arm was used. At each visit, after the patient was in a sitting position with the back supported and both feet placed on the floor for 5 minutes, systolic and diastolic BP were measured 3 times with an automated BP monitor and appropriate size cuff. Means of the 3 measurements were calculated. A negative change indicates lowered BP. (NCT00765674)
Timeframe: Baseline to end of study (Week 8)

InterventionmmHg (Least Squares Mean)
Aliskiren / Amlodipine-31.37
Aliskiren / Hydrochlorothiazide-27.99
Amlodipine / Hydrochlorothiazide-30.77
Aliskiren / Amlodipine / Hydrochlorothiazide-37.92

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Percentage of Participants (Defined as Estimated Cumulative Control Rate) Reaching Blood Pressure Target in a Stepped Care, Aliskiren-based Regimen

For non diabetic patients the Blood Pressure target is defined as mean sitting Systolic Blood Pressure [msSBP] < 140 mmHg and mean sitting Diastolic Blood Pressure [msDBP] < 90 mmHg and for diabetic patients the Blood Pressure target is mean sitting Systolic Blood Pressure [msSBP] < 130 mmHg and mean sitting Diastolic Blood Pressure [msDBP] < 80 mmHg. (NCT00765947)
Timeframe: 24 weeks

InterventionPercentage of participants (Number)
Aliskiren-based Regimen86.12

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Changes From Baseline to Week 24 in Mean Sitting Systolic Blood Pressure [msSBP] and Mean Sitting Diastolic Blood Pressure [msDBP]

(NCT00765947)
Timeframe: Baseline and Week 24

Interventionmm Hg (Mean)
msSBPmsDBP
Aliskiren-based Regimen-25.33-12.40

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Percent of Responders for Mean Sitting Systolic Blood Pressure [msSBP] and for Mean Sitting Diastolic Blood Pressure [msDBP]

Response for mean sitting Systolic Blood Pressure [msSBP] is defined as a reduction of ≥ 20 mmHg from baseline or mean sitting Systolic Blood Pressure [msSBP] < 140 mmHg (non diabetics) or < 130 mmHg (diabetics). Response for mean sitting Diastolic Blood Pressure [msDBP] is defined as a reduction of ≥10 mmHg from baseline or mean sitting Diastolic Blood Pressure [msDBP] < 90 mmHg (non diabetic) or < 80 mmHg (diabetics). (NCT00765947)
Timeframe: 24 weeks

InterventionPercentage of Participants (Number)
msSBPmsDBP
Aliskiren-based Regimen96.8097.78

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Percentage of Patients (Defined as Estimated Cumulative Control Rate) Reaching Blood Pressure Target in a Stepped-care, Aliskiren-based Regimen by Patient Subgroups of Mild and Moderate Hypertensive Patients, and Non-diabetic and Diabetic Patients.

For non diabetic patients the Blood Pressure target is defined as mean sitting Systolic Blood Pressure [msSBP] < 140 mmHg and mean sitting Diastolic Blood Pressure [msDBP] < 90 mmHg and for diabetic patients the Blood Pressure target is mean sitting Systolic Blood Pressure [msSBP] < 130 mmHg and mean sitting Diastolic Blood Pressure [msDBP] < 80 mmHg. (NCT00765947)
Timeframe: 24 weeks

InterventionPercentage of Participants (Number)
Mild HypertensiveModerate HypertensiveNon-diabeticDiabetic
Aliskiren-based Regimen91.4879.2492.7472.58

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Change From Baseline in Mean Sitting Systolic Blood Pressure (MSSBP)

To assess the change in mean sitting systolic blood pressure (MSSBP) after 8 weeks of treatment with aliskiren HCTZ (150/12.5 mg, 300/25 mg) versus ramipril (5 mg, 10 mg). (NCT00772577)
Timeframe: Baseline to week 8

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from baseline to week 8
Aliskiren HCTZ167.0138.9-28.1
Ramipril168.2151.6-16.6

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Percentage of Responders (MSSBP < 140 mmHg or ≥ 20 mmHg Decrease From Baseline in MSSBP)

To compare the percentage of responders (as defined by patients with MSSBP < 140 mm Hg or a decrease from baseline ≥ 20 mm Hg) during 8 weeks of treatment with aliskiren HCTZ (150/12.5 mg, 300/25 mg) versus ramipril (5 mg, 10 mg). Data presented are cumulative. Cumulative refers to achieving the response before or at the 8 week visit. If response occurred more than once, only the first occurrence was counted. (NCT00772577)
Timeframe: 8 weeks

InterventionPercentage of patients (Number)
Aliskiren HCTZ87.9
Ramipril63.2

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (MSDBP)

To evaluate the difference in mean sitting diastolic blood pressure (MSDBP) after 8 weeks of treatment with aliskiren HCTZ (150/12.5 mg, 300/25 mg) versus ramipril (5 mg, 10 mg). (NCT00772577)
Timeframe: Baseline to week 8

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from baseline to week 8
Aliskiren HCTZ94.384.2-10.1
Ramipril96.392.7-3.6

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Change From Baseline in Mean Sitting Pulse Pressure (MSPP)

To compare the change in mean sitting pulse pressure (MSPP) after 8 weeks of treatment with aliskiren HCTZ (150/12.5 mg, 300/25 mg) versus ramipril (5 mg, 10 mg). (NCT00772577)
Timeframe: Baseline to week 8

,
Interventionmm Hg (Mean)
BaselineWeek 8Change from baseline to week 8
Aliskiren HCTZ72.754.7-18.0
Ramipril71.958.9-13.0

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Percentage of Patients Achieving Blood Pressure Control During 8 Weeks

The percentage of patients achieving the Blood Pressure control (defined as patients achieving a MSSBP < 140 mm Hg and MSDBP < 90 mm Hg) during 8 weeks of treatment with aliskiren HCTZ (150/12.5 mg, 300/25 mg) versus ramipril (5 mg, 10 mg). Data presented are cumulative. Cumulative refers to achieving blood pressure control before or at the 8 week visit. If achieving blood pressure control occurred more than once, only the first occurrence was counted. (NCT00772577)
Timeframe: 8 weeks

InterventionPercentage of patients (Number)
Aliskiren HCTZ63.7
Ramipril30.0

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Percentage of Responders

Response defined by mean sitting Systolic Blood Pressure < 130 mm Hg or a reduction of mean sitting Systolic Blood Pressure >= 20 mm Hg from baseline (NCT00787605)
Timeframe: Week 8

InterventionPercentage of Participants (Number)
Aliskiren/HCTZ74.2
Amlodipine68.5

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)

(NCT00787605)
Timeframe: Baseline and Week 8

InterventionmmHg (Least Squares Mean)
Aliskiren/HCTZ-9.92
Amlodipine-8.97

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Biomarker Measurements

Geometric mean of the post to baseline ratio in biomarkers of plasma renin activity (ng/ml/h), plasma renin concentration (ng/L), and cystatin C (mg/L) (NCT00787605)
Timeframe: Baseline and Week 8

,
Interventionratio (Geometric Mean)
Plasma Renin activity (ng/ml/h) (N= 317, 300)Plasma Renin concentration (ng/L) (N=315, 299)Cystatin C (mg/L) (N = 327 , 310)
Aliskiren/HCTZ0.429.531.04
Amlodipine1.751.490.98

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)

(NCT00787605)
Timeframe: Baseline and Week 8

InterventionmmHg (Least Squares Mean)
Aliskiren/HCTZ-28.82
Amlodipine-26.22

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Evaluate the Safety and Tolerability

Percentage of patients with Adverse Event and percentage of patients with edema (NCT00787605)
Timeframe: after 8 weeks of treatment

,
InterventionPercentage of participants (Number)
Any Adverse Eventedema
Aliskiren/HCTZ36.02.6
Amlodipine48.317.6

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Percentage of Patients Achieving Blood Pressure Control

Blood pressure control is defined as patient achieving a target Blood Pressure of mean sitting Systolic BloodPressure / mean sitting Diastolic Blood Pressure < 130/80 mmHg. (NCT00787605)
Timeframe: after 8 weeks of treatment

InterventionPercentage of Participants (Number)
Aliskiren/HCTZ23.2
Amlodipine13.8

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Percentage of Obese Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=4954 weeks: >15 and ≤ 30 mm Hg, N=4954 weeks: >30 and ≤ 45 mm Hg, N=4954 weeks: >45 mm Hg, N=4958 weeks: ≤ 15 mm Hg, N=4688 weeks: >15 and ≤ 30 mm Hg, N=4688 weeks: >30 and ≤ 45 mm Hg, N=4688 weeks: >45 mm Hg, N=46812 weeks: ≤ 15 mm Hg, N=43612 weeks: >15 and ≤ 30 mm Hg, N=43612 weeks: >30 and ≤ 45 mm Hg, N=43612 weeks: >45 mm Hg, N=43616 weeks: ≤ 15 mm Hg, N=40016 weeks: >15 and ≤ 30 mm Hg, N=40016 weeks: >30 and ≤ 45 mm Hg, N=40016 weeks: >45 mm Hg, N=40020 weeks: ≤ 15 mm Hg, N=37920 weeks: >15 and ≤ 30 mm Hg, N=37920 weeks: >30 and ≤ 45 mm Hg, N=37920 weeks: >45 mm Hg, N=379
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide56.035.28.50.452.435.910.31.537.842.417.42.527.836.027.58.820.637.533.38.7

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Percentage of Participants Previously on an Angiotensin Converting Enzyme Inhibitor Achieving the Blood Pressure Goals From Baseline to 20 Weeks

(NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide91.584.571.447.498.289.878.590.571.061.544.5

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Percentage of Participants Previously on an Angiotensin Converting Enzyme Inhibitor Achieving the Blood Pressure Goals From Baseline to 12 Weeks

(NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide81.369.353.031.594.480.664.378.552.743.527.9

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Percentage of Participants Previously on a Nondihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks

(NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide100.0100.095.045.0100.095.095.0100.095.095.040.0

[back to top]

Percentage of Patients With Metabolic Syndrome Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=4544 weeks: <85 mm Hg, N=4544 weeks: <80 mm Hg, N=4548 weeks: <90 mm Hg, N=4578 weeks: <85 mm Hg, N=4578 weeks: <80 mm Hg, N=45712 weeks: <90 mm Hg, N=45712 weeks: <85 mm Hg, N=45712 weeks: <80 mm Hg, N=45716 weeks: <90 mm Hg, N=45716 weeks: <85 mm Hg, N=45716 weeks: <80 mm Hg, N=45720 weeks: <90 mm Hg, N=45720 weeks: <85 mm Hg, N=45720 weeks: <80 mm Hg, N=457
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide69.653.531.982.166.143.590.476.656.594.883.265.995.486.272.0

[back to top]

Percentage of Patients With Metabolic Syndrome Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=4534 weeks: >10 and ≤ 15 mm Hg, N=4534 weeks: >15 and ≤ 20 mm Hg, N=4534 weeks: >20 mm Hg, N=4538 weeks: ≤ 10 mm Hg, N=4318 weeks: >10 and ≤ 15 mm Hg, N=4318 weeks: >15 and ≤ 20 mm Hg, N=4318 weeks: >20 mm Hg, N=43112 weeks: ≤ 10 mm Hg, N=40212 weeks: >10 and ≤15 mm Hg, N=40212 weeks: >15 and ≤ 20 mm Hg, N=40212 weeks: >20 mm Hg, N=40216 weeks: ≤ 10 mm Hg, N=37116 weeks: >10 and ≤ 15 mm Hg, N=37116 weeks: >15 and ≤ 20 mm Hg, N=37116 weeks: >20 mm Hg, N=37120 weeks: ≤ 10 mm Hg, N=35620 weeks: >10 and ≤ 15 mm Hg, N=35620 weeks: >15 and ≤ 20 mm Hg, N=35620 weeks: >20 mm Hg, N=356
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide62.722.38.66.456.619.715.38.444.322.117.416.232.424.021.022.633.219.422.525.0

[back to top]

Percentage of Patients With Metabolic Syndrome Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=4544 weeks: <135 mm Hg, N=4544 weeks: <130 mm Hg, N=4544 weeks: <120 mm Hg, N=4548 weeks: <140 mm Hg, N=4578 weeks: <135 mm Hg, N=4578 weeks: <130 mm Hg, N=4578 weeks: <120 mm Hg, N=45712 weeks: <140 mm Hg, N=45712 weeks: <135 mm Hg, N=45712 weeks: <130 mm Hg, N=45712 weeks: <120 mm Hg, N=45716 weeks: <140 mm Hg, N=45716 weeks: <135 mm Hg, N=45716 weeks: <130 mm Hg, N=45716 weeks: <120 mm Hg, N=45720 weeks: <140 mm Hg, N=45720 weeks: <135 mm Hg, N=45720 weeks: <130 mm Hg, N=45720 weeks: <120 mm Hg, N=457
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide56.441.427.17.967.654.340.916.281.467.254.127.688.880.367.039.091.585.674.847.1

[back to top]

Percentage of Patients With Metabolic Syndrome Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=4534 weeks: >15 and ≤ 30 mm Hg, N=4534 weeks: >30 and ≤ 45 mm Hg, N=4534 weeks: >45 mm Hg, N=4538 weeks: ≤ 15 mm Hg, N=4318 weeks: >15 and ≤ 30 mm Hg, N=4318 weeks: >30 and ≤ 45 mm Hg, N=4318 weeks: >45 mm Hg, N=43112 weeks: ≤ 15 mm Hg, N=40212 weeks: >15 and ≤ 30 mm Hg, N=40212 weeks: >30 and ≤ 45 mm Hg, N=40212 weeks: >45 mm Hg, N=40216 weeks: ≤ 15 mm Hg, N=37116 weeks: >15 and ≤ 30 mm Hg, N=37116 weeks: >30 and ≤ 45 mm Hg, N=37116 weeks: >45 mm Hg, N=37120 weeks: ≤ 15 mm Hg, N=35620 weeks: >15 and ≤ 30 mm Hg, N=35620 weeks: >30 and ≤ 45 mm Hg, N=35620 weeks: >45 mm Hg, N=356
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide49.538.411.50.748.035.514.42.130.443.822.63.224.037.729.19.219.736.536.07.9

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Percentage of Asain Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=1284 weeks: <85 mm Hg, N=1284 weeks: <80 mm Hg, N=1288 weeks: <90 mm Hg, N=1288 weeks: <85 mm Hg, N=1288 weeks: <80 mm Hg, N=12812 weeks: <90 mm Hg, N=12812 weeks: <85 mm Hg, N=12812 weeks: <80 mm Hg, N=12816 weeks: <90 mm Hg, N=12816 weeks: <85 mm Hg, N=12816 weeks: <80 mm Hg, N=12820 weeks: <90 mm Hg, N=12820 weeks: <85 mm Hg, N=12820 weeks: <80 mm Hg, N=128
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide83.669.545.389.179.760.295.387.571.196.993.082.096.993.085.2

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Percentage of Participants Previously on a Nondihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks

(NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide100.090.075.025.0100.095.075.0100.070.065.020.0

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Percentage of Participants Previously on a Diuretic Achieving the Blood Pressure Goals From Baseline to 20 Weeks

(NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide92.882.578.351.294.686.871.788.667.565.148.2

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Percentage of Participants Previously on a Diuretic Achieving the Blood Pressure Goals From Baseline to 12 Weeks

(NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide92.882.578.351.294.686.871.788.667.565.148.2

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Percentage of Participants Achieving the Mean 24-hour Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 12 Weeks

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. (NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
24-hour mean systolic blood pressure <140 mmHg24-hour mean systolic blood pressure <135 mmHg24-hour mean systolic blood pressure <130 mmHg24-hour mean systolic blood pressure <120 mmHg24-hour mean diastolic blood pressure <90 mmHg24-hour mean diastolic blood pressure <85 mmHg24-hour mean diastolic blood pressure <80 mmHg24-hour mean blood pressure <140/90 mmHg24-hour mean blood pressure <135/95 mmHg24-hour mean blood pressure <135/80 mmHg24-hour mean blood pressure <130/80 mmHg24-hour mean blood pressure <125/75 mmHg24-hour mean blood pressure <120/80 mmHg24-hour mean blood pressure <120/70 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide95.690.479.947.298.796.184.794.389.180.373.452.445.927.5

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The Percentage of Subjects Who Achieve BP Goal (<140/90 mmHg for Non-diabetics or <130/80 mmHg for Diabetics) From Baseline to 12 and 20 Weeks

(NCT00791258)
Timeframe: Baseline to 12 and 20 weeks

InterventionPercentage of participants (Number)
12 weeks20 weeks
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide71.384.8

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Percentage of Type 2 Diabetic Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=1894 weeks: >15 and ≤ 30 mm Hg, N=1894 weeks: >30 and ≤ 45 mm Hg, N=1894 weeks: >45 mm Hg, N=1898 weeks: ≤ 15 mm Hg, N=1818 weeks: >15 and ≤ 30 mm Hg, N=1818 weeks: >30 and ≤ 45 mm Hg, N=1818 weeks: >45 mm Hg, N=18112 weeks: ≤ 15 mm Hg, N=17012 weeks: >15 and ≤ 30 mm Hg, N=17012 weeks: >30 and ≤ 45 mm Hg, N=17012 weeks: >45 mm Hg, N=17016 weeks: ≤ 15 mm Hg, N=15616 weeks: >15 and ≤ 30 mm Hg, N=15616 weeks: >30 and ≤ 45 mm Hg, N=15616 weeks: >45 mm Hg, N=15620 weeks: ≤ 15 mm Hg, N=15020 weeks: >15 and ≤ 30 mm Hg, N=15020 weeks: >30 and ≤ 45 mm Hg, N=15020 weeks: >45 mm Hg, N=150
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide56.136.07.90.054.134.311.60.035.338.222.93.528.240.426.35.126.040.026.77.3

[back to top]

Percentage of Type 2 Diabetic Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=1904 weeks: <135 mm Hg, N=1904 weeks: <130 mm Hg, N=1904 weeks: <120 mm Hg, N=1908 weeks: <140 mm Hg, N=1908 weeks: <135 mm Hg, N=1908 weeks: <130 mm Hg, N=1908 weeks: <120 mm Hg, N=19012 weeks: <140 mm Hg, N=19012 weeks: <135 mm Hg, N=19012 weeks: <130 mm Hg, N=19012 weeks: <120 mm Hg, N=19016 weeks: <140 mm Hg, N=19016 weeks: <135 mm Hg, N=19016 weeks: <130 mm Hg, N=19016 weeks: <120 mm Hg, N=19020 weeks: <140 mm Hg, N=19020 weeks: <135 mm Hg, N=19020 weeks: <130 mm Hg, N=19020 weeks: <120 mm Hg, N=190
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide54.741.126.310.069.056.342.615.881.669.557.930.087.979.069.039.591.184.275.348.4

[back to top]

Percentage of Type 2 Diabetic Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=1894 weeks: >10 and ≤ 15 mm Hg, N=1894 weeks: >15 and ≤ 20 mm Hg, N=1894 weeks: >20 mm Hg, N=1898 weeks: ≤ 10 mm Hg, N=1818 weeks: >10 and ≤ 15 mm Hg, N=1818 weeks: >15 and ≤ 20 mm Hg, N=1818 weeks: >20 mm Hg, N=18112 weeks: ≤ 10 mm Hg, N=17012 weeks: >10 and ≤15 mm Hg, N=17012 weeks: >15 and ≤ 20 mm Hg, N=17012 weeks: >20 mm Hg, N=17016 weeks: ≤ 10 mm Hg, N=15616 weeks: >10 and ≤ 15 mm Hg, N=15616 weeks: >15 and ≤ 20 mm Hg, N=15616 weeks: >20 mm Hg, N=15620 weeks: ≤ 10 mm Hg, N=15020 weeks: >10 and ≤ 15 mm Hg, N=15020 weeks: >15 and ≤ 20 mm Hg, N=15020 weeks: >20 mm Hg, N=150
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide67.716.911.63.760.820.414.93.941.232.412.913.532.726.921.818.637.318.026.018.7

[back to top]

Percentage of Type 2 Diabetic Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=1904 weeks: <85 mm Hg, N=1904 weeks: <80 mm Hg, N=1908 weeks: <90 mm Hg, N=1908 weeks: <85 mm Hg, N=1908 weeks: <80 mm Hg, N=19012 weeks: <90 mm Hg, N=19012 weeks: <85 mm Hg, N=19012 weeks: <80 mm Hg, N=19016 weeks: <90 mm Hg, N=19016 weeks: <85 mm Hg, N=19016 weeks: <80 mm Hg, N=19020 weeks: <90 mm Hg, N=19020 weeks: <85 mm Hg, N=19020 weeks: <80 mm Hg, N=190
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide75.864.239.085.872.651.194.283.263.797.989.070.599.090.576.8

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Percentage of Participants Achieving the Mean 24-hour Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 20 Weeks

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. (NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
24-hour mean systolic blood pressure <140 mmHg24-hour mean systolic blood pressure <135 mmHg24-hour mean systolic blood pressure <130 mmHg24-hour mean systolic blood pressure <120 mmHg24-hour mean diastolic blood pressure <90 mmHg24-hour mean diastolic blood pressure <85 mmHg24-hour mean diastolic blood pressure <80 mmHg24-hour mean blood pressure <140/90 mmHg24-hour mean blood pressure <135/95 mmHg24-hour mean blood pressure <135/80 mmHg24-hour mean blood pressure <130/80 mmHg24-hour mean blood pressure <125/75 mmHg24-hour mean blood pressure <120/80 mmHg24-hour mean blood pressure <120/70 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide99.597.594.570.4100.097.593.099.596.092.590.575.470.455.3

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Percentage of Participants Achieving the Mean Daytime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 12 Weeks

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. Daytime is defined as 8AM - 4PM. (NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Daytime mean systolic blood pressure <140 mmHgDaytime mean systolic blood pressure <135 mmHgDaytime mean systolic blood pressure <130 mmHgDaytime mean systolic blood pressure <120 mmHgDaytime mean diastolic blood pressure <90 mmHgDaytime mean diastolic blood pressure <85 mmHgDaytime mean diastolic blood pressure <80 mmHgDaytime mean blood pressure <140/90 mmHgDaytime mean blood pressure <135/95 mmHgDaytime mean blood pressure <135/80 mmHgDaytime mean blood pressure <130/80 mmHgDaytime mean blood pressure <125/75 mmHgDaytime mean blood pressure <120/80 mmHgDaytime mean blood pressure <120/70 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide88.279.966.428.895.683.065.586.972.961.153.331.927.913.1

[back to top]

Percentage of Participants Achieving the Mean Daytime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 20 Weeks

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. Daytime is defined as 8AM - 4PM. (NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Daytime mean systolic blood pressure <140 mmHgDaytime mean systolic blood pressure <135 mmHgDaytime mean systolic blood pressure <130 mmHgDaytime mean systolic blood pressure <120 mmHgDaytime mean diastolic blood pressure <90 mmHgDaytime mean diastolic blood pressure <85 mmHgDaytime mean diastolic blood pressure <80 mmHgDaytime mean blood pressure <140/90 mmHgDaytime mean blood pressure <135/95 mmHgDaytime mean blood pressure <135/80 mmHgDaytime mean blood pressure <130/80 mmHgDaytime mean blood pressure <125/75 mmHgDaytime mean blood pressure <120/80 mmHgDaytime mean blood pressure <120/70 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide96.593.583.951.898.592.583.995.088.481.977.456.851.333.2

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Percentage of Participants Achieving the Mean Nighttime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 12 Weeks

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. Nighttime is defined as 10p.m. - 6 a.m. (NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Nighttime mean systolic blood pressure <140 mmHgNighttime mean systolic blood pressure <135 mmHgNighttime mean systolic blood pressure <130 mmHgNighttime mean systolic blood pressure <120 mmHgNighttime mean diastolic blood pressure <90 mmHgNighttime mean diastolic blood pressure <85 mmHgNighttime mean diastolic blood pressure <80 mmHgNighttime mean blood pressure <140/90 mmHgNighttime mean blood pressure <135/95 mmHgNighttime mean blood pressure <135/80 mmHgNighttime mean blood pressure <130/80 mmHgNighttime mean blood pressure <125/75 mmHgNighttime mean blood pressure <120/80 mmHgNighttime mean blood pressure <120/70 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide97.894.392.674.799.698.394.897.493.490.889.177.774.262.0

[back to top]

Percentage of Participants Achieving the Mean Nighttime Blood Pressure Goals, as Measured by Ambulatory Blood Pressure Monitor, From Baseline to 20 Weeks

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. Nighttime is defined as 10 p.m. - 6 a.m. (NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Nighttime mean systolic blood pressure <140 mmHgNighttime mean systolic blood pressure <135 mmHgNighttime mean systolic blood pressure <130 mmHgNighttime mean systolic blood pressure <120 mmHgNighttime mean diastolic blood pressure <90 mmHgNighttime mean diastolic blood pressure <85 mmHgNighttime mean diastolic blood pressure <80 mmHgNighttime mean blood pressure <140/90 mmHgNighttime mean blood pressure <135/95 mmHgNighttime mean blood pressure <135/80 mmHgNighttime mean blood pressure <130/80 mmHgNighttime mean blood pressure <125/75 mmHgNighttime mean blood pressure <120/80 mmHgNighttime mean blood pressure <120/70 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide99.599.597.586.499.598.596.099.098.596.095.088.985.978.9

[back to top]

Percentage of Participants Previously on a Dihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks

(NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide89.783.869.241.091.585.569.285.564.159.836.8

[back to top]

Percentage of Obese Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=4974 weeks: <135 mm Hg, N=4974 weeks: <130 mm Hg, N=4974 weeks: <120 mm Hg, N=4978 weeks: <140 mm Hg, N=5008 weeks: <135 mm Hg, N=5008 weeks: <130 mm Hg, N=5008 weeks: <120 mm Hg, N=50012 weeks: <140 mm Hg, N=50012 weeks: <135 mm Hg, N=50012 weeks: <130 mm Hg, N=50012 weeks: <120 mm Hg, N=50016 weeks: <140 mm Hg, N=50016 weeks: <135 mm Hg, N=50016 weeks: <130 mm Hg, N=50016 weeks: <120 mm Hg, N=50020 weeks: <140 mm Hg, N=50020 weeks: <135 mm Hg, N=50020 weeks: <130 mm Hg, N=50020 weeks: <120 mm Hg, N=500
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide51.337.223.37.963.249.237.013.876.661.649.223.285.875.663.634.690.282.672.243.0

[back to top]

Percentage of Obese Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=4954 weeks: >10 and ≤ 15 mm Hg, N=4954 weeks: >15 and ≤ 20 mm Hg, N=4954 weeks: >20 mm Hg, N=4958 weeks: ≤ 10 mm Hg, N=4688 weeks: >10 and ≤ 15 mm Hg, N=4688 weeks: >15 and ≤ 20 mm Hg, N=4688 weeks: >20 mm Hg, N=46812 weeks: ≤ 10 mm Hg, N=43612 weeks: >10 and ≤15 mm Hg, N=43612 weeks: >15 and ≤ 20 mm Hg, N=43612 weeks: >20 mm Hg, N=43616 weeks: ≤ 10 mm Hg, N=40016 weeks: >10 and ≤ 15 mm Hg, N=40016 weeks: >15 and ≤ 20 mm Hg, N=40016 weeks: >20 mm Hg, N=40020 weeks: ≤ 10 mm Hg, N=37920 weeks: >10 and ≤ 15 mm Hg, N=37920 weeks: >15 and ≤ 20 mm Hg, N=37920 weeks: >20 mm Hg, N=379
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide67.517.88.56.359.419.913.07.748.922.516.112.633.323.019.024.831.918.722.426.9

[back to top]

Percentage of Obese Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=4974 weeks: <85 mm Hg, N=4974 weeks: <80 mm Hg, N=4978 weeks: <90 mm Hg, N=4978 weeks: <85 mm Hg, N=5008 weeks: <80 mm Hg, N=50012 weeks: <90 mm Hg, N=50012 weeks: <85 mm Hg, N=50012 weeks: <80 mm Hg, N=50016 weeks: <90 mm Hg, N=50016 weeks: <85 mm Hg, N=50016 weeks: <80 mm Hg, N=50020 weeks: <90 mm Hg, N=50020 weeks: <85 mm Hg, N=50020 weeks: <80 mm Hg, N=500
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide63.246.326.077.259.438.886.669.848.493.280.460.494.683.867.6

[back to top]

Percentage of Asian Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=1264 weeks: >10 and ≤ 15 mm Hg, N=1264 weeks: >15 and ≤ 20 mm Hg, N=1264 weeks: >20 mm Hg, N=1268 weeks: ≤ 10 mm Hg, N=1238 weeks: >10 and ≤ 15 mm Hg, N=1238 weeks: >15 and ≤ 20 mm Hg, N=1238 weeks: >20 mm Hg, N=12312 weeks: ≤ 10 mm Hg, N=12012 weeks: >10 and ≤15 mm Hg, N=12012 weeks: >15 and ≤ 20 mm Hg, N=12012 weeks: >20 mm Hg, N=12016 weeks: ≤ 10 mm Hg, N=11216 weeks: >10 and ≤ 15 mm Hg, N=11216 weeks: >15 and ≤ 20 mm Hg, N=11216 weeks: >20 mm Hg, N=11220 weeks: ≤ 10 mm Hg, N=10520 weeks: >10 and ≤ 15 mm Hg, N=10520 weeks: >15 and ≤ 20 mm Hg, N=10520 weeks: >20 mm Hg, N=105
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide47.626.213.512.738.224.422.015.533.325.819.221.727.717.020.534.836.216.218.129.5

[back to top]

Percentage of Participants Previously on an Angiotensin II Receptor Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks

(NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide80.869.256.026.189.776.959.076.152.646.223.1

[back to top]

Percentage of Participants Previously on an Angiotensin II Receptor Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks

(NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide92.387.279.547.496.689.374.890.670.165.044.0

[back to top]

Percentage of Patients Achieving Seated Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140/90 mm Hg, N=9754 weeks: <135/80 mm Hg, N=9754 weeks: <130/80 mm Hg, N=9754 weeks: <120/80 mm Hg, N=9758 weeks: <140/90 mm Hg, N=9298 weeks: <135/80 mm Hg, N=9298 weeks: <130/80 mm Hg, N=9298 weeks: <120/80 mm Hg, N=92912 weeks: <140/90 mm Hg, N=86512 weeks: <135/80 mm Hg, N=86512 weeks: <130/80 mm Hg, N=86512 weeks: <120/80 mm Hg, N=86516 weeks: <140/90mm Hg, N=79716 weeks: <135/80mm Hg, N=79716 weeks: <130/80mm Hg, N=79716 weeks: <120/80mm Hg, N=79720 weeks: <140/90 mm Hg, N=74520 weeks: <135/80 mm Hg, N=74520 weeks: <130/80 mm Hg, N=74520 weeks: <120/80 mm Hg, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide49.123.017.37.852.429.824.811.268.140.034.317.677.851.346.228.781.355.650.128.2

[back to top]

Percentage of Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of participants (Number)
4 weeks: <90 mm Hg, N=9754weeks: <85 mm Hg, N=9754 weeks: <80 mm Hg, N=9758 weeks: <90 mm Hg, N=9298 weeks: <85 mm Hg, N=9298 weeks: <80 mm Hg, N=92912 weeks: <90 mm Hg, N=86512 weeks: <85 mm Hg, N=86512 weeks: <80 mm Hg, N=86516 weeks: <90 mm Hg, N=79716 weeks: <85 mm Hg, N=79716 weeks: <80 mm Hg, N=79720 weeks: <90 mm Hg, N=74520 weeks: <85 mm Hg, N=74520 weeks: <80 mm Hg, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide71.355.234.275.157.140.284.368.749.590.276.959.689.779.562.0

[back to top]

Percentage of Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=9754 weeks: >10 and ≤ 15 mm Hg, N=9754 weeks: >15 and ≤ 20 mm Hg, N=9754 weeks: >20 mm Hg, N=9758 weeks: ≤ 10 mm Hg, N=9298 weeks: >10 and ≤ 15 mm Hg, N=9298 weeks: >15 and ≤ 20 mm Hg, N=9298 weeks: >20 mm Hg, N=92912 weeks: ≤ 10 mm Hg, N=86512 weeks: >10 and ≤ 15 mm Hg, N=86512 weeks: >15 and ≤ 20 mm Hg, N=86512 weeks: >20 mm Hg, N=86516 weeks: ≤ 10 mm Hg, N=79716 weeks: >10 and ≤ 15 mm Hg, N=79716 weeks: >15 and ≤ 20 mm Hg, N=79716 weeks: >20 mm Hg, N=79720 weeks: ≤ 10 mm Hg, N=74520 weeks: >10 and ≤ 15 mm Hg, N=74520 weeks: >15 and ≤ 20 mm Hg, N=74520 weeks: >20 mm Hg, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide61.321.010.57.254.720.714.110.643.824.115.816.330.422.821.525.431.419.922.626.2

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Percentage of Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=9754 weeks: <135 mm Hg, N=9754 weeks: <130 mm Hg, N=9754 weeks: <120 mm Hg, N=9758 weeks: <140 mm Hg, N=9298 weeks: <135 mm Hg, N=9298 weeks: <130 mm Hg, N=9298 weeks: <120 mm Hg, N=92912 weeks: <140 mm Hg, N=86512 weeks: <135 mm Hg, N=86512 weeks: <130 mm Hg, N=86512 weeks: <120 mm Hg, N=86516 weeks: <140 mm Hg, N=79716 weeks: <135 mm Hg, N=79716 weeks: <130 mm Hg, N=79716 weeks: <120 mm Hg, N=79720 weeks: <140 mm Hg, N=74520 weeks: <135 mm Hg, N=74520 weeks: <130 mm Hg, N=74520 weeks: <120 mm Hg, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide54.239.825.38.957.245.935.012.972.659.045.319.480.970.358.930.984.375.264.231.5

[back to top]

Percentage of Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=9754 weeks: >15 and ≤ 30 mm Hg, N=9754 weeks: >30 and ≤ 45 mm Hg, N=9754 weeks: >45 mm Hg, N=9758 weeks: ≤ 15 mm Hg, N=9298 weeks: >15 and ≤ 30 mm Hg, N=9298 weeks: >30 and ≤ 45 mm Hg, N=9298 weeks: >45 mm Hg, N=92912 weeks: ≤ 15 mm Hg, N=86512 weeks: >15 and ≤ 30 mm Hg, N=86512 weeks: >30 and ≤ 45 mm Hg, N=86512 weeks: >45 mm Hg, N=86516 weeks: ≤ 15 mm Hg, N=79716 weeks: >15 and ≤ 30 mm Hg, N=79716 weeks: >30 and ≤ 45 mm Hg, N=79716 weeks: >45 mm Hg, N=79720 weeks: ≤ 15 mm Hg, N=74520 weeks: >15 and ≤ 30 mm Hg, N=74520 weeks: >30 and ≤ 45 mm Hg, N=74520 weeks: >45 mm Hg, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide51.436.610.51.545.837.714.32.330.543.122.43.923.235.932.08.920.436.234.09.4

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Percentage of Participants Previously on a Beta Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks

(NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide88.575.262.033.694.783.261.186.755.849.629.2

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Percentage of Participants Previously on a Beta Blocker Achieving the Blood Pressure Goals From Baseline to 20 Weeks

(NCT00791258)
Timeframe: Baseline to 20 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide93.887.679.747.898.289.477.092.974.369.943.4

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Percentage of Elderly Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=2244 weeks: >10 and ≤ 15 mm Hg, N=2244 weeks: >15 and ≤ 20 mm Hg, N=2244 weeks: >20 mm Hg, N=2248 weeks: ≤ 10 mm Hg, N=2178 weeks: >10 and ≤ 15 mm Hg, N=2178 weeks: >15 and ≤ 20 mm Hg, N=2178 weeks: >20 mm Hg, N=21712 weeks: ≤ 10 mm Hg, N=19912 weeks: >10 and ≤15 mm Hg, N=19912 weeks: >15 and ≤ 20 mm Hg, N=19912 weeks: >20 mm Hg, N=19916 weeks: ≤ 10 mm Hg, N=17916 weeks: >10 and ≤ 15 mm Hg, N=17916 weeks: >15 and ≤ 20 mm Hg, N=17916 weeks: >20 mm Hg, N=17920 weeks: ≤ 10 mm Hg, N=16620 weeks: >10 and ≤ 15 mm Hg, N=16620 weeks: >15 and ≤ 20 mm Hg, N=16620 weeks: >20 mm Hg, N=166
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide63.820.59.46.357.119.814.38.845.225.115.614.127.425.122.924.634.920.524.120.5

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Percentage of Participants Previously on a Dihydropyridine Calcium Channel Blocker Achieving the Blood Pressure Goals From Baseline to 12 Weeks

(NCT00791258)
Timeframe: Baseline to 12 weeks

InterventionPercentage of participants (Number)
Systolic blood pressure <140 mmHgSystolic blood pressure <135 mmHgSystolic blood pressure <130 mmHgSystolic blood pressure <120 mmHgDiastolic blood pressure <90 mmHgDiastolic blood pressure <85 mmHgDiastolic blood pressure <80 mmHgBlood pressure <140/90 mmHgBlood pressure <135/80 mmHgBlood pressure <130/80 mmHgBlood pressure <120/80 mmHg
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide73.559.047.918.886.372.748.768.440.234.216.2

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Percentage of Hispanic Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=984 weeks: >15 and ≤ 30 mm Hg, N=984 weeks: >30 and ≤ 45 mm Hg, N=984 weeks: >45 mm Hg, N=988 weeks: ≤ 15 mm Hg, N=918 weeks: >15 and ≤ 30 mm Hg, N=918 weeks: >30 and ≤ 45 mm Hg, N=918 weeks: >45 mm Hg, N=9112 weeks: ≤ 15 mm Hg, N=8312 weeks: >15 and ≤ 30 mm Hg, N=8312 weeks: >30 and ≤ 45 mm Hg, N=8312 weeks: >45 mm Hg, N=8316 weeks: ≤ 15 mm Hg, N=7516 weeks: >15 and ≤ 30 mm Hg, N=7516 weeks: >30 and ≤ 45 mm Hg, N=7516 weeks: >45 mm Hg, N=7520 weeks: ≤ 15 mm Hg, N=7120 weeks: >15 and ≤ 30 mm Hg, N=7120 weeks: >30 and ≤ 45 mm Hg, N=7120 weeks: >45 mm Hg, N=71
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide50.037.87.15.142.944.09.93.331.336.125.37.222.736.034.76.723.933.833.88.5

[back to top]

Percentage of Hispanic Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=984 weeks: <135 mm Hg, N=984 weeks: <130 mm Hg, N=984 weeks: <120 mm Hg, N=988 weeks: <140 mm Hg, N=1008 weeks: <135 mm Hg, N=1008 weeks: <130 mm Hg, N=1008 weeks: <120 mm Hg, N=10012 weeks: <140 mm Hg, N=10012 weeks: <135 mm Hg, N=10012 weeks: <130 mm Hg, N=10012 weeks: <120 mm Hg, N=10016 weeks: <140 mm Hg, N=10016 weeks: <135 mm Hg, N=10016 weeks: <130 mm Hg, N=10016 weeks: <120 mm Hg, N=10020 weeks: <140 mm Hg, N=10020 weeks: <135 mm Hg, N=10020 weeks: <130 mm Hg, N=10020 weeks: <120 mm Hg, N=100
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide55.139.831.610.264.051.041.015.077.067.054.030.084.077.066.037.088.083.072.041.0

[back to top]

Percentage of Hispanic Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=984 weeks: >10 and ≤ 15 mm Hg, N=984 weeks: >15 and ≤ 20 mm Hg, N=984 weeks: >20 mm Hg, N=988 weeks: ≤ 10 mm Hg, N=918 weeks: >10 and ≤ 15 mm Hg, N=918 weeks: >15 and ≤ 20 mm Hg, N=918 weeks: >20 mm Hg, N=9112 weeks: ≤ 10 mm Hg, N=8312 weeks: >10 and ≤15 mm Hg, N=8312 weeks: >15 and ≤ 20 mm Hg, N=8312 weeks: >20 mm Hg, N=8316 weeks: ≤ 10 mm Hg, N=7516 weeks: >10 and ≤ 15 mm Hg, N=7516 weeks: >15 and ≤ 20 mm Hg, N=7516 weeks: >20 mm Hg, N=7520 weeks: ≤ 10 mm Hg, N=7120 weeks: >10 and ≤ 15 mm Hg, N=7120 weeks: >15 and ≤ 20 mm Hg, N=7120 weeks: >20 mm Hg, N=71
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide65.316.38.210.252.818.714.314.341.020.514.524.130.725.316.028.031.012.726.829.6

[back to top]

Percentage of Hispanic Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=984 weeks: <85 mm Hg, N=984 weeks: <80 mm Hg, N=988 weeks: <90 mm Hg, N=1008 weeks: <85 mm Hg, N=1008 weeks: <80 mm Hg, N=10012 weeks: <90 mm Hg, N=10012 weeks: <85 mm Hg, N=10012 weeks: <80 mm Hg, N=10016 weeks: <90 mm Hg, N=10016 weeks: <85 mm Hg, N=10016 weeks: <80 mm Hg, N=10020 weeks: <90 mm Hg, N=10020 weeks: <85 mm Hg, N=10020 weeks: <80 mm Hg, N=100
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide66.353.134.785.070.048.092.078.062.096.090.075.096.090.075.0

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Percentage of Elderly Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=2244 weeks: >15 and ≤ 30 mm Hg, N=2244 weeks: >30 and ≤ 45 mm Hg, N=2244 weeks: >45 mm Hg, N=2248 weeks: ≤ 15 mm Hg, N=2178 weeks: >15 and ≤ 30 mm Hg, N=2178 weeks: >30 and ≤ 45 mm Hg, N=2178 weeks: >45 mm Hg, N=21712 weeks: ≤ 15 mm Hg, N=19912 weeks: >15 and ≤ 30 mm Hg, N=19912 weeks: >30 and ≤ 45 mm Hg, N=19912 weeks: >45 mm Hg, N=19916 weeks: ≤ 15 mm Hg, N=17916 weeks: >15 and ≤ 30 mm Hg, N=17916 weeks: >30 and ≤ 45 mm Hg, N=17916 weeks: >45 mm Hg, N=17920 weeks: ≤ 15 mm Hg, N=16620 weeks: >15 and ≤ 30 mm Hg, N=16620 weeks: >30 and ≤ 45 mm Hg, N=16620 weeks: >45 mm Hg, N=166
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide47.340.211.21.342.937.816.62.826.646.724.62.017.932.439.710.114.537.438.010.2

[back to top]

Percentage of Elderly Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=2274 weeks: <135 mm Hg, N=2274 weeks: <130 mm Hg, N=2274 weeks: <120 mm Hg, N=2278 weeks: <140 mm Hg, N=2278 weeks: <135 mm Hg, N=2278 weeks: <130 mm Hg, N=2278 weeks: <120 mm Hg, N=22712 weeks: <140 mm Hg, N=22712 weeks: <135 mm Hg, N=22712 weeks: <130 mm Hg, N=22712 weeks: <120 mm Hg, N=22716 weeks: <140 mm Hg, N=22716 weeks: <135 mm Hg, N=22716 weeks: <130 mm Hg, N=22716 weeks: <120 mm Hg, N=22720 weeks: <140 mm Hg, N=22720 weeks: <135 mm Hg, N=22720 weeks: <130 mm Hg, N=22720 weeks: <120 mm Hg, N=227
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide52.037.923.49.767.057.743.618.180.670.056.828.687.779.770.943.691.685.978.950.7

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Change in Mean Seated Systolic Blood Pressure From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

Interventionmm Hg (Mean)
4 weeks, N=9758 weeks, N=92912 weeks, N=86516 weeks, N=79720 weeks, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide-14.6-16.6-21.8-26.0-26.8

[back to top]

Percentage of Elderly Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=2274 weeks: <85 mm Hg, N=2274 weeks: <80 mm Hg, N=2278 weeks: <90 mm Hg, N=2278 weeks: <85 mm Hg, N=2278 weeks: <80 mm Hg, N=22712 weeks: <90 mm Hg, N=22712 weeks: <85 mm Hg, N=22712 weeks: <80 mm Hg, N=22716 weeks: <90 mm Hg, N=22716 weeks: <85 mm Hg, N=22716 weeks: <80 mm Hg, N=22720 weeks: <90 mm Hg, N=22720 weeks: <85 mm Hg, N=22720 weeks: <80 mm Hg, N=227
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide88.176.758.292.183.771.897.492.180.298.794.388.698.795.290.3

[back to top]

Percentage of Asian Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=1284 weeks: <135 mm Hg, N=1284 weeks: <130 mm Hg, N=1284 weeks: <120 mm Hg, N=1288 weeks: <140 mm Hg, N=1288 weeks: <135 mm Hg, N=1288 weeks: <130 mm Hg, N=1288 weeks: <120 mm Hg, N=12812 weeks: <140 mm Hg, N=12812 weeks: <135 mm Hg, N=12812 weeks: <130 mm Hg, N=12812 weeks: <120 mm Hg, N=12816 weeks: <140 mm Hg, N=12816 weeks: <135 mm Hg, N=12816 weeks: <130 mm Hg, N=12816 weeks: <120 mm Hg, N=12820 weeks: <140 mm Hg, N=12820 weeks: <135 mm Hg, N=12820 weeks: <130 mm Hg, N=12820 weeks: <120 mm Hg, N=128
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide64.851.635.211.776.667.251.625.089.178.966.438.395.389.881.347.797.793.085.951.6

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The Percentage of Patients Who Achieve Seated Systolic Blood Pressure Goal (<140 mm Hg for Non-diabetics and <130 mm Hg for Diabetics) From Baseline to 12 Weeks

(NCT00791258)
Timeframe: baseline to 12 weeks

InterventionPercentage of participants (Number)
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide75.8

[back to top]

Percentage of Asian Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=1264 weeks: >15 and ≤ 30 mm Hg, N=1264 weeks: >30 and ≤ 45 mm Hg, N=1264 weeks: >45 mm Hg, N=1268 weeks: ≤ 15 mm Hg, N=1238 weeks: >15 and ≤ 30 mm Hg, N=1238 weeks: >30 and ≤ 45 mm Hg, N=1238 weeks: >45 mm Hg, N=12312 weeks: ≤ 15 mm Hg, N=12012 weeks: >15 and ≤ 30 mm Hg, N=12012 weeks: >30 and ≤ 45 mm Hg, N=12012 weeks: >45 mm Hg, N=12016 weeks: ≤ 15 mm Hg, N=11216 weeks: >15 and ≤ 30 mm Hg, N=11216 weeks: >30 and ≤ 45 mm Hg, N=11216 weeks: >45 mm Hg, N=11220 weeks: ≤ 15 mm Hg, N=10520 weeks: >15 and ≤ 30 mm Hg, N=10520 weeks: >30 and ≤ 45 mm Hg, N=10520 weeks: >45 mm Hg, N=105
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide43.738.115.92.440.735.822.01.628.339.227.55.020.536.631.311.629.528.633.38.6

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The Percentage of Subjects Achieving Seated Diastolic BP Goal (<90 mmHg for Non-diabetics or < 80 mmHg for Subjects With Diabetes) From Baseline to 12 Weeks

(NCT00791258)
Timeframe: baseline to 12 weeks

InterventionPercentage of participants (Number)
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide84.3

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Change From Baseline to Week 12 in Ambulatory Systolic and Diastolic Blood Pressure Values

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. Daytime is defined as 8 a.m. to 4 p.m. Nighttime is defined as 10 p.m. to 6 a.m. (NCT00791258)
Timeframe: Baseline to 12 weeks

Interventionmm Hg (Mean)
24-hour mean systolic blood pressureMean daytime systolic blood pressureMean nighttime systolic blood pressureSystolic blood pressure - last 2 hours of doseSystolic blood pressure - last 4 hours of doseSystolic blood pressure - last 6 hours of dose24-hour mean diastolic blood pressureMean daytime diastolic blood pressureMean nighttime diastolic blood pressureDiastolic blood pressure - last 2 hours of doseDiastolic blood pressure - last 4 hours of doseDiastolic blood pressure - last 6 hours of dose
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide-14.8-16.3-12.5-13.6-13.0-12.6-9.4-10.6-7.6-8.6-8.0-7.7

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Change From Baseline to Week 20 in Ambulatory Systolic and Diastolic Blood Pressure Values

Once the Ambulatory Blood Pressure Monitor (ABPM) has been applied, the dose of medication was taken and the subject wore the ABPM for a period of 24 hours. Daytime is defined as 8 a.m. to 4 p.m. Nighttime is defined as 10 p.m. to 6 a.m. (NCT00791258)
Timeframe: Baseline to 20 weeks

Interventionmm Hg (Mean)
24-hour mean systolic blood pressureMean daytime systolic blood pressureMean nighttime systolic blood pressureSystolic blood pressure - last 2 hours of doseSystolic blood pressure - last 4 hours of doseSystolic blood pressure - last 6 hours of dose24-hour mean diastolic blood pressureMean daytime diastolic blood pressureMean nighttime diastolic blood pressureDiastolic blood pressure - last 2 hours of doseDiastolic blood pressure - last 4 hours of doseDiastolic blood pressure - last 6 hours of dose
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide-21.0-23.2-17.5-19.6-18.2-17.9-13.3-15.0-11.1-12.3-11.6-11.3

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Change in Mean Seated Diastolic Blood Pressure From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

Interventionmm Hg (Mean)
4 weeks, N=9758 weeks, N=92912 weeks, N=86516 weeks, N=79720 weeks, N=745
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide-8.1-9.1-11.9-14.6-14.5

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Percentage of African American/Black Patients Achieving Seated Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140/90 mm Hg, N=2304 weeks: <135/80 mm Hg, N=2304 weeks: <130/80 mm Hg, N=2304 weeks: <120/80 mm Hg, N=2308 weeks: <140/90 mm Hg, N=2318 weeks: <135/80 mm Hg, N=2318 weeks: <130/80 mm Hg, N=2328 weeks: <120/80 mm Hg, N=23212 weeks: <140/90mm Hg, N=23212 weeks: <135/80 mm Hg, N=23212 weeks: <130/80 mm Hg, N=23212 weeks: <120/80 mm Hg, N=23216 weeks: <140/90 mm Hg, N=23216 weeks: <135/80 mm Hg, N=23216 weeks: <130/80 mm Hg, N=23216 weeks: <120/80 mm Hg, N=23220 weeks: <140/90 mm Hg, N=23220 weeks: <135/80 mm Hg, N=23220 weeks: <130/80 mm Hg, N=23220 weeks: <120/80 mm Hg, N=232
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide45.714.810.43.955.023.820.810.468.538.435.816.480.649.147.430.686.657.855.239.7

[back to top]

Percentage of African American/Black Patients Achieving Seated Diastolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <90 mm Hg, N=2304 weeks: <85 mm Hg, N=2304 weeks: <80 mm Hg, N=2308 weeks: <90 mm Hg, N=2318 weeks: <85 mm Hg, N=2318 weeks: <80 mm Hg, N=23112 weeks: <90 mm Hg, N=23212 weeks: <85 mm Hg, N=23212 weeks: <80 mm Hg, N=23216 weeks: <90 mm Hg, N=23216 weeks: <85 mm Hg, N=23216 weeks: <80 mm Hg, N=23220 weeks: <90 mm Hg, N=23220 weeks: <85 mm Hg, N=23220 weeks: <80 mm Hg, N=232
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide60.942.219.671.953.730.382.366.045.392.276.355.294.880.661.2

[back to top]

Percentage of African American/Black Patients Achieving Seated Diastolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 10 mm Hg, N=2304 weeks: >10 and ≤ 15 mm Hg, N=2304 weeks: >15 and ≤ 20 mm Hg, N=2304 weeks: >20 mm Hg, N=2308 weeks: ≤ 10 mm Hg, N=2208 weeks: >10 and ≤ 15 mm Hg, N=2208 weeks: >15 and ≤ 20 mm Hg, N=2208 weeks: >20 mm Hg, N=22012 weeks: ≤ 10 mm Hg, N=20812 weeks: >10 and ≤15 mm Hg, N=20812 weeks: >15 and ≤ 20 mm Hg, N=20812 weeks: >20 mm Hg, N=20816 weeks: ≤ 10 mm Hg, N=19916 weeks: >10 and ≤ 15 mm Hg, N=19916 weeks: >15 and ≤ 20 mm Hg, N=19916 weeks: >20 mm Hg, N=19920 weeks: ≤ 10 mm Hg, N=18920 weeks: >10 and ≤ 15 mm Hg, N=18920 weeks: >15 and ≤ 20 mm Hg, N=18920 weeks: >20 mm Hg, N=189
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide70.017.87.94.466.815.010.97.354.821.212.012.038.719.623.118.636.019.620.623.8

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Percentage of African American/Black Patients Achieving Seated Systolic Blood Pressure Goal From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: <140 mm Hg, N=2304 weeks: <135 mm Hg, N=2304 weeks: <130 mm Hg, N=2304 weeks: <120 mm Hg, N=2308 weeks: <140 mm Hg, N=2318 weeks: <135 mm Hg, N=2318 weeks: <130 mm Hg, N=2318 weeks: <120 mm Hg, N=23112 weeks: <140 mm Hg, N=23212 weeks: <135 mm Hg, N=23212 weeks: <130 mm Hg, N=23212 weeks: <120 mm Hg, N=23216 weeks: <140 mm Hg, N=23216 weeks: <135 mm Hg, N=23216 weeks: <130 mm Hg, N=23216 weeks: <120 mm Hg, N=23220 weeks: <140 mm Hg, N=23220 weeks: <135 mm Hg, N=23220 weeks: <130 mm Hg, N=23220 weeks: <120 mm Hg, N=232
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide51.734.419.65.762.344.633.813.076.359.147.019.884.971.161.234.191.080.671.144.4

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Percentage of African American/Black Patients Achieving Seated Systolic Blood Pressure Reduction Ranges From Baseline to 4, 8, 12, 16, 20 Weeks

(NCT00791258)
Timeframe: Baseline to 4, 8, 12, 16, 20 weeks

InterventionPercentage of Participants (Number)
4 weeks: ≤ 15 mm Hg, N=2304 weeks: >15 and ≤ 30 mm Hg, N=2304 weeks: >30 and ≤ 45 mm Hg, N=2304 weeks: >45 mm Hg, N=2308 weeks: ≤ 15 mm Hg, N=2208 weeks: >15 and ≤ 30 mm Hg, N=2208 weeks: >30 and ≤ 45 mm Hg, N=2208 weeks: >45 mm Hg, N=22012 weeks: ≤ 15 mm Hg, N=20812 weeks: >15 and ≤ 30 mm Hg, N=20812 weeks: >30 and ≤ 45 mm Hg, N=20812 weeks: >45 mm Hg, N=20816 weeks: ≤ 15 mm Hg, N=19916 weeks: >15 and ≤ 30 mm Hg, N=19916 weeks: >30 and ≤ 45 mm Hg, N=19916 weeks: >45 mm Hg, N=19920 weeks: ≤ 15 mm Hg, N=18920 weeks: >15 and ≤ 30 mm Hg, N=18920 weeks: >30 and ≤ 45 mm Hg, N=18920 weeks: >45 mm Hg, N=189
Olmesartan Medoxomil/Amlodipine Tablets + Hydrochlorothiazide60.032.27.40.453.638.27.30.938.941.816.42.930.737.225.17.024.337.629.68.5

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Change From Baseline to Week 8 in Pulse Pressure

(NCT00797316)
Timeframe: Baseline and Week 8

Interventionmm Hg (Least Squares Mean)
Aliskiren/HCTZ-18.96
Aliskiren-13.33

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Percentage of Patients Achieving Blood Pressure Control at Week 8

Blood pressure control is defined as a patient who achieves a target Blood Pressure of mean sitting Systolic Blood Pressure / mean sitting Diastolic Blood pressure < 140/90 mmHg. (NCT00797316)
Timeframe: 8 weeks

InterventionPercentage of Participants (Number)
Aliskiren/HCTZ58.7
Aliskiren34.5

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Change From Baseline to Week 8 in Mean Sitting Diastolic Blood Pressure (msDBP)

(NCT00797316)
Timeframe: 8 weeks

Interventionmm Hg (Least Squares Mean)
Aliskiren/HCTZ-11.26
Aliskiren-6.90

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Change From Baseline to Week 8 in Mean Sitting Systolic Blood Pressure (msSBP)

(NCT00797316)
Timeframe: Baseline and Week 8

Interventionmm Hg (Least Squares Mean)
Aliskiren/HCTZ-30.38
Aliskiren-20.15

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Percentage of Participants With Blood Pressure Response at Week 8

Response is defined as a patient with msSBP < 140 mmHg or a decrease from baseline ≥ 20 mmHg in msSBP during eight weeks of treatment. (NCT00797316)
Timeframe: 8 weeks

InterventionPercentage of Participants (Number)
Aliskiren/HCTZ78.4
Aliskiren55.2

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Percentage of Participants Achieving Overall Blood Pressure Control at 8, 16, 24 and 32 Weeks Endpoints

Systolic & Diastolic Blood Pressure were measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and after 8, 16 , 24 and 32 weeks. Outcome is reported as percentage of participants achieving overall blood pressure control (msSBP <140 mmHg and msDBP <90 mmHg) at weeks 8, 16, 24 & 32 endpoints. (NCT00797862)
Timeframe: Baseline to week 8, 16, 24 and 32 endpoints

,,
InterventionPercentage of Participants (Number)
Week 8 endpointWeek 16 endpointWeek 24 endpointWeek 32 endpoint
Aliskiren Start-Amlodipine Add On22.833.362.859.0
Aliskiren+Amlodipine46.565.963.461.6
Amlodipine Start-Aliskiren Add On25.240.957.853.4

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP) at Week 24

Diastolic Blood pressure was measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and 24 weeks of study treatment. Analysis used a repeated measures ANCOVA model with treatment, visit and region, as factors, treatment by visit interaction and baseline msDBP as a covariate. (NCT00797862)
Timeframe: Baseline to 24 weeks

InterventionmmHg (Least Squares Mean)
Aliskiren+Amlodipine-13.64
Aliskiren Start-Amlodipine Add On-13.22
Amlodipine Start-Aliskiren Add On-12.25

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Overall Mean Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) Over 8, 16 and 24 Weeks

Systolic Blood Pressure was measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and over 8, 16 and 24 weeks of study treatment. The overall mean change in msSBP from baseline was estimated over three time points: Week 8, Week 16, and Week 24. Analysis used a repeated measures Analysis of Covariance (ANCOVA) model with treatment, visit, and region as factors, treatment by visit interaction and baseline msSBP as a covariate. (NCT00797862)
Timeframe: Baseline, 8 weeks, 16 weeks, and 24 weeks

InterventionmmHg (Least Squares Mean)
Aliskiren+Amlodipine-25.34
Aliskiren Start-Amlodipine Add On-17.94
Amlodipine Start-Aliskiren Add On-19.81

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP) at Week 32

Diastolic Blood Pressure was measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and 32 weeks of study treatment. Change at Week 32 used a separate repeated measures ANCOVA model containing Week 8, 16, 24 and 32 data. Treatment, visit and region were factors in the model, treatment by visit interaction and baseline msDBP a covariate. (NCT00797862)
Timeframe: Baseline to 32 weeks

InterventionmmHg (Least Squares Mean)
Aliskiren+Amlodipine-12.96
Aliskiren Start-Amlodipine Add On-12.96
Amlodipine Start-Aliskiren Add On-11.62

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) at Week 24

Systolic Blood pressure was measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and 24 weeks of study treatment. Analysis used a repeated measures ANCOVA model with treatment, visit and region as factors, treatment by visit interaction and baseline msSBP as a covariate. (NCT00797862)
Timeframe: Baseline to 24 weeks

InterventionmmHg (Least Squares Mean)
Aliskiren+Amlodipine-27.37
Aliskiren Start-Amlodipine Add On-26.34
Amlodipine Start-Aliskiren Add On-25.52

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) at Week 32

Systolic Blood pressure was measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and 32 weeks of study treatment. Change at week 32 used a separate repeated measures ANCOVA model containing Week 8, 16, 24 & 32 data. Treatment, visit and region were factors in the model, treatment by visit interaction and baseline msSBP was a covariate. (NCT00797862)
Timeframe: Baseline to 32 weeks

InterventionmmHg (Least Squares Mean)
Aliskiren+Amlodipine-26.42
Aliskiren Start-Amlodipine Add On-25.75
Amlodipine Start-Aliskiren Add On-24.32

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Overall Mean Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP) Over 8, 16, and 24 Weeks

Diastolic Blood pressure was measured in a sitting position using a validated automated blood pressure monitor (the Omron device) according to Guidelines of the British Hypertension Society, at Baseline and over 8, 16 and 24 weeks of study treatment. The overall mean change in msDBP from baseline was estimated over three time points: Week 8, Week 16, and Week 24. Analysis used a repeated measures ANCOVA model with treatment, visit and regions as factors, treatment by visit interaction and baseline msDBP as a covariate. (NCT00797862)
Timeframe: Baseline, 8 weeks, 16 weeks and 24 weeks

InterventionmmHg (Least Squares Mean)
Aliskiren+Amlodipine-12.39
Aliskiren Start-Amlodipine Add On-8.37
Amlodipine Start-Aliskiren Add On-9.02

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Percentage of Participants Who Reached Their Trough, Sitting, Clinic Systolic and Diastolic Blood Pressure Targets, Defined as <140/90 mm Hg Without Diabetes or Chronic Kidney Disease or <130/80 mm Hg With Diabetes or Chronic Kidney Disease

Percentage of participants who achieve both a clinic systolic and diastolic blood pressure response measured at each week indicated, defined as <140/90 mm Hg for participants without diabetes or chronic kidney disease or <130/80 mm Hg for participants with diabetes or chronic kidney disease[GFR <60 mL/min/1.73 m2 or urinary albumin:creatinine ratio (UACR) >200 mg albumin/g creatinine at Screening.] Systolic/diastolic blood pressure is the average of the 3 serial trough sitting systolic/diastolic blood pressure measurements. (NCT00818883)
Timeframe: Week 2, Week 4, Week 6, Week 8 and Week 10.

,
Interventionpercentage of participants (Number)
Week 2 (n=283; n=276)Week 4 (n=292; n=289)Week 6 (n=295; n=292)Week 8 (n=295; n=292)Week 10 (n=295; n=292)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD24.645.345.959.262.3
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD27.258.664.172.571.5

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Percentage of Participants Who Reached Their Trough, Sitting, Clinic Systolic Blood Pressure Targets, Defined as <140 mm Hg for Participants Without Diabetes or Chronic Kidney Disease or <130 mm Hg for Participants With Diabetes or Chronic Kidney Disease

Percentage of participants who achieve a clinic systolic blood pressure response measured at each week indicated, defined as <140mm Hg without diabetes or chronic kidney disease or <130/mm Hg with diabetes or chronic kidney disease. Systolic blood pressure is the average of the 3 serial trough sitting systolic blood pressure measurements. (NCT00818883)
Timeframe: Week 2, Week 4, Week 6, Week 8 and Week 10.

,
Interventionpercentage of participants (Number)
Week 2 (n=283; n=276)Week 4 (n=292; n=289)Week 6 (n=295; n=292)Week 8 (n=295; n=292)Week 10 (n=295; n=292)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD34.154.758.265.469.9
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD33.268.271.979.776.9

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Change From Baseline in the Mean Nighttime (12 AM to 6 AM) Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in nighttime (12am to 6am) mean systolic blood pressure measured at each visit indicated including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Nighttime mean is the average of all measurements recorded between the hours of 12 am and 6 am. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-18.8-21.1
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-21.8-23.8

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Change From Baseline in 24-hour Mean Diastolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in 24-hour mean diastolic blood pressure measured at each visit indicated including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-10.9-12.6
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-14.7-15.2

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Change From Baseline in 24-hour Mean Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in 24-hour mean systolic blood pressure measured at each visit indicated including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179, n=162)Week 10 (n=227, n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-19.9-22.4
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-25.7-26.6

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Change From Baseline in Mean Trough Diastolic Blood Pressure (22 to 24 Hours After Dosing) as Measured by Ambulatory Blood Pressure Monitoring.

The change in trough diastolic blood pressure measured at each week indicated including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The trough is the average of all measurements recorded from 22 to 24 hours after dosing. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-10.6-12.7
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-15.2-15.1

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Change From Baseline in Mean Trough Systolic Blood Pressure (22 to 24 Hours After Dosing) as Measured by Ambulatory Blood Pressure Monitoring.

The change in trough systolic blood pressure measured at each week indicated including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The trough is the average of all measurements recorded from 22 to 24 hours after dosing. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179, n=162)Week 10 (n=227, n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-18.4-21.4
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-25.7-25.6

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Change From Baseline in the Mean Daytime (6 AM to 10 PM) Diastolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in daytime (6am to 10pm) mean diastolic blood pressure measured at each visit including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of all measurements recorded between the hours of 6 am and 10 pm. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-11.1-12.9
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-15.4-15.8

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Change From Baseline in the Mean Daytime (6 AM to 10 PM) Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in daytime (6am to 10pm) mean systolic blood pressure measured at each visit including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of all measurements recorded between the hours of 6 am and 10 pm. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-20.2-22.8
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-27.0-27.5

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Change From Baseline in the Mean Diastolic Blood Pressure at 0 to 12 Hours After Dosing as Measured by Ambulatory Blood Pressure Monitoring.

The change in the 12-hour mean diastolic blood pressure measured at each visit including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 12-hour mean is the average of all measurements recorded in the first 12 hours after dosing. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-11.1-12.9
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-15.7-16.0

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Change From Baseline in the Mean Nighttime (12 AM to 6 AM) Diastolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in nighttime (12am to 6am) mean diastolic blood pressure measured at each visit indicated including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Nighttime mean is the average of all measurements recorded between the hours of 12 am and 6 am. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-10.3-11.9
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-12.8-13.8

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Change From Baseline in the Mean Systolic Blood Pressure at 0 to 12 Hours After Dosing as Measured by Ambulatory Blood Pressure Monitoring

The change in the 12-hour mean systolic blood pressure measured at each visit including final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 12-hour mean is the average of all measurements recorded in the first 12 hours after dosing. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=179; n=162)Week 10 (n=227; n=230)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-20.6-23.2
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-27.7-28.0

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Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure

The change in sitting trough clinic diastolic blood pressure measured at each week indicated including final visit relative to baseline. Diastolic blood pressure is the average of the 3 serial trough sitting systolic blood pressure measurements. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=295; n=292)Week 10 (n=295; n=292)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-11.2-13.7
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-15.0-16.4

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Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure

The change in sitting trough clinic systolic blood pressure measured at each week indicated including final visit relative to baseline. Systolic blood pressure is the average of the 3 serial trough sitting systolic blood pressure measurements. (NCT00818883)
Timeframe: Baseline, Week 6 and Week 10.

,
InterventionmmHg (Least Squares Mean)
Week 6 (n=295; n=292)Week 10 (n=295; n=292)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD-29.5-32.8
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD-35.1-37.8

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Percentage of Participants Who Reached Their Trough, Sitting, Clinic Diastolic Blood Pressure Target, Defined as <90 mm Hg for Participants Without Diabetes or Chronic Kidney Disease or <80 mm Hg for Participants With Diabetes or Chronic Kidney Disease.

Percentage of participants who achieve a clinic diastolic blood pressure response measured at each week indicated, defined as <90 mm Hg for participants without diabetes or chronic kidney disease or <80 mm Hg for participants with diabetes or chronic kidney disease. Diastolic blood pressure is the average of the 3 serial trough sitting diastolic blood pressure measurements. (NCT00818883)
Timeframe: Week 2, Week 4, Week 6, Week 8 and Week 10.

,
Interventionpercentage of participants (Number)
Week 2 (n=283; n=276)Week 4 (n=292; n=289)Week 6 (n=295; n=292)Week 8 (n=295; n=292)Week 10 (n=295; n=292)
Azilsartan Medoxomil 40 mg + Hydrochlorothiazide 12.5 mg QD41.357.459.272.375.0
Azilsartan Medoxomil 40 mg/Chlorthalidone 12.5 mg QD49.171.976.681.482.7

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Chloriuretic Response to a Thiaizde

Change from baseline in fractional chloride excretion in response to a single dose of hydrochlorothiazide (NCT00822107)
Timeframe: 6 hours

Interventionfractional chloride excretion (Mean)
Thiazide Response1.23

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Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexipril.

Bioequivalence based on Cmax. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng/mL (Mean)
Test (Moexipril HCl/HCTZ)14.487
Reference (Uniretic®)14.885

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Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Hydrochlorothiazide.

Bioequivalence based on Cmax. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng/mL (Mean)
Test (Moexipril HCl/HCTZ)150.225
Reference (Uniretic®)148.39

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AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexiprilat.

Informational comparison of AUC0-t values for the metabolite Moexiprilat. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)215.654
Reference (Uniretic®)214.286

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AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexipril.

Bioequivalence based on AUC0-t. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)35.412
Reference (Uniretic®)34.917

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AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexipril.

Bioequivalence based on AUC0-inf. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)36.651
Reference (Uniretic®)35.74

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Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexiprilat.

Informational comparison of Cmax values for the metabolite Moexiprilat. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng/mL (Mean)
Test (Moexipril HCl/HCTZ)5.512
Reference (Uniretic®)5.13

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AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Hydrochlorothiazide.

Bioequivalence based on AUC0-t. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)1105.63
Reference (Uniretic®)1100.5

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AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexiprilat.

Informational comparison of AUC0-inf values for the metabolite Moexiprilat. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)376.814
Reference (Uniretic®)379.994

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AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Hydrochlorothiazide.

Bioequivalence based on AUC0-inf. (NCT00834067)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)1115.905
Reference (Uniretic®)1108.329

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AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Hydrochlorothiazide.

Bioequivalence based on AUC0-inf. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)1001.133
Reference (Uniretic®)1001.548

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AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexipril.

Bioequivalence based on AUC0-inf. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)55.837
Reference (Uniretic®)54.593

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AUC0-inf (Area Under the Concentration-time Curve From Time Zero to Infinity) of Moexiprilat.

Informational comparison of AUC0-inf values for the metabolite Moexiprilat. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)443.448
Reference (Uniretic®)427.212

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AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexipril.

Bioequivalence based on AUC0-t. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)54.517
Reference (Uniretic®)53.598

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Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexipril.

Bioequivalence based on Cmax. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng/mL (Mean)
Test (Moexipril HCl/HCTZ)31.913
Reference (Uniretic®)34.4

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Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Hydrochlorothiazide.

Bioequivalence based on Cmax. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng/mL (Mean)
Test (Moexipril HCl/HCTZ)153.602
Reference (Uniretic®)145.088

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AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Moexiprilat.

Informational comparison of AUC0-t values for the metabolite Moexiprilat. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)262.231
Reference (Uniretic®)264.991

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Cmax (Maximum Observed Concentration of Drug Substance in Plasma) of Moexiprilat.

Informational comparison of Cmax values for the metabolite Moexiprilat. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng/mL (Mean)
Test (Moexipril HCl/HCTZ)20.049
Reference (Uniretic®)21.882

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AUC0-t (Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration) of Hydrochlorothiazide.

Bioequivalence based on AUC0-t. (NCT00835042)
Timeframe: Blood samples collected over a 192 hour period.

Interventionng*h/mL (Mean)
Test (Moexipril HCl/HCTZ)992.17
Reference (Uniretic®)994.093

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Change From Baseline in Nighttime Mean (12am to 6am) Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in the nighttime, while asleep (12am to 6am) mean diastolic blood pressure measured at Week 4 and Week 8 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Nighttime mean is the average (arithmetic mean) of measurements recorded between the hours of 12 AM (inclusive) and 6 AM (exclusive) included in the 24-hour mean calculations. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-13.4-14.9
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-13.3-15.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-9.6-11.8

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Change From Baseline in Nighttime Mean (12am to 6am) Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring

The change in the nighttime, while asleep (12am to 6am) mean systolic blood pressure measured at Week 4 and Week 8 to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Nighttime mean is the average of measurements recorded between the hours of 12 AM (inclusive) and 6 AM (exclusive) included in the 24-hour mean calculations. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-22.3-25.2
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-21.9-26.3
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-16.6-19.7

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Change From Baseline in Trough Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in trough systolic blood pressure measured at week 4 and week 8 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Trough is the average of all measurements recorded from 22 to 24 hours after dosing. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-13.4-14.6
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-14.6-15.9
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-10.9-12.0

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Change From Baseline in Trough Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in trough systolic blood pressure measured at week 4 and week 8 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Trough is the average of all measurements recorded from 22 to 24 hours after dosing. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-22.4-24.9
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-23.6-26.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-17.4-19.6

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Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure

The change in trough diastolic blood pressure measured at week 4 and week 8 relative to baseline. Diastolic blood pressure is the average of the 3 serial trough sitting diastolic blood pressure measurements. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=360; n=347; n=352)Week 8 (n=363; n=350; n=353)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-13.6-16.1
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-14.2-16.5
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-10.4-12.8

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Percentage of Participants Who Achieve a Clinic Diastolic AND Systolic Blood Pressure Response, Defined as <140/90 mm Hg for Participants Without Diabetes or Chronic Kidney Disease (CKD) or <130/80 mm Hg for Participants With Diabetes or CKD

Percentage of participants who achieve both a clinic diastolic blood pressure response, defined as <140/90 mm Hg for participants without diabetes or chronic kidney disease (CKD) or <130/80 mm Hg for participants with diabetes or CKD at each time frame relative to baseline. (NCT00846365)
Timeframe: Baseline, Week 2, Week 4, Week 6 and Week 8.

,,
Interventionpercentage of participants (Number)
Week 2 (n=343; n=334; n=345)Week 4 (n=360; n=347; n=352)Week 6 (n=362; n=350; n=353)Week 8 (n=363; n=350; n=353)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD51.358.168.869.4
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD48.561.465.468.9
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD35.944.655.554.7

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Percentage of Participants Who Achieve a Clinic Diastolic Blood Pressure Response, Defined as Defined as <90 mm Hg for Participants Without Diabetes or CKD or <80 mm Hg for Participants With Diabetes or CKD

Percentage of participants who achieve a clinic diastolic blood pressure response, defined as defined as <90 mm Hg for participants without diabetes or CKD or <80 mm Hg for participants with diabetes or CKD at each time frame relative to baseline. (NCT00846365)
Timeframe: Baseline, Week 2, Week 4, Week 6 and Week 8.

,,
Interventionpercentage of participants (Number)
Week 2 (n=343; n=334; n=345)Week 4 (n=360; n=347; n=352)Week 6 (n=362; n=350; n=353)Week 8 (n=363; n=350; n=353)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD63.671.477.979.9
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD66.273.876.979.1
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD47.858.266.966.0

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Percentage of Participants Who Achieve a Clinic Systolic Blood Pressure Response, Defined as <140 mm Hg for Participants Without Diabetes or CKD or <130 mm Hg for Participants With Diabetes or CKD

Percentage of participants who achieve a clinic systolic blood pressure response, defined as <140 mm Hg for participants without diabetes or CKD or <130 mm Hg for participants with diabetes or CKD at each time frame relative to baseline. (NCT00846365)
Timeframe: Baseline, Week 2, Week 4, Week 6 and Week 8.

,,
Interventionpercentage of participants (Number)
Week 2 (n=343; n=334; n=345)Week 4 (n=360; n=347; n=352)Week 6 (n=362; n=350; n=353)Week 8 (n=363; n=350; n=353)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD60.366.176.876.0
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD57.268.973.476.0
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD44.952.364.964.6

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Change From Baseline in 12-hr Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in the 0 to 12 hours-after-dosing mean diastolic blood pressure measured at Week 4 and Week 8 to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The mean consists of the average (arithmetic mean) of measurements collected at each time frame and includes all observations recorded over the subsequent 12 hours. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-14.4-15.4
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-14.8-16.9
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-10.8-12.1

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Change From Baseline to Week 4 in Trough, Sitting, Clinic Systolic Blood Pressure.

The change in trough systolic blood pressure measured at week 4 relative to baseline. Systolic blood pressure is the average of the 3 serial trough sitting systolic blood pressure measurements. (NCT00846365)
Timeframe: Baseline and Week 4.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-33.0
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-34.1
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-26.9

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Change From Baseline to Week 8 in Trough, Sitting, Clinic Systolic Blood Pressure.

The change in trough systolic blood pressure measured at week 8 or final visit relative to baseline. Systolic blood pressure is the average of the 3 serial trough sitting systolic blood pressure measurements. (NCT00846365)
Timeframe: Baseline and Week 8.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-37.6
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-38.2
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-31.5

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Change From Baseline in 12-hr Mean Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in the 0 to 12 hours-after-dosing mean Systolic Blood Pressure measured at Week 4 and Week 8 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night The mean consists of the average (arithmetic mean) of measurements collected at each time frame and includes all observations recorded over the subsequent 12 hours. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-25.0-27.1
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-25.5-28.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-19.2-21.1

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Change From Baseline in 24-hour Mean Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in the 0 to 24-hours-after-dosing mean diastolic blood pressure measured at Week 4 and Week 8 relative to baseline. . Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The mean consists of the average of measurements collected over the subsequent 24 hours. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-13.9-15.1
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-14.4-16.4
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-10.5-12.0

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Change From Baseline in 24-hour Mean Systolic Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring.

The change in the 24-hour mean systolic blood pressure at week4 and week 8 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-24.1-26.4
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-24.4-27.9
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-18.4-20.7

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Change From Baseline in Daytime Mean (6am to 10pm) Diastolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in the daytime, while awake (6am to 10pm) mean diastolic blood pressure measured at Week 4 and Week 8relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of measurements recorded between the hours of 6 AM (inclusive) and 10 PM (exclusive) included in the 24-hour mean calculations. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-14.2-15.3
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-14.7-16.6
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-10.7-12.1

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Change From Baseline in Daytime Mean (6am to 10pm) Systolic Blood Pressure Measured by Ambulatory Blood Pressure Monitoring.

The change in the daytime, while awake (6am to 10pm) mean systolic blood pressure measured at Week 4 and Week 8 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night Daytime mean is the average of measurements recorded between the hours of 6 AM (inclusive) and 10 PM (exclusive) included in the 24-hour mean calculations. (NCT00846365)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=223; n=227; n=219)Week 8 (n=290; n=278; n=281)
Azilsartan Medoxomil 20-40mg Plus Chlorthalidone 12.5-25 mg QD-24.5-26.7
Azilsartan Medoxomil 40-80mg Plus Chlorthalidone 12.5-25 mg QD-25.1-28.4
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-18.9-21.0

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Mitral Annulus Velocities on Tissue Doppler (Delta E/e' Ratio), a Measure of Diastolic Function (With Angiotensin II)

Diastolic function was assessed via tissue doppler imaging (TDI) by echocardiography to determine left ventricular diastolic function before and after 6 months of treatment; and in response to acute administration (3 nanograms/kg/min for 60 min) of the vasoactive agent, Angiotensin II. (NCT00865124)
Timeframe: Baseline and six months

,,
Interventionratio (Mean)
Pre-treatment, E/e', baselinePre-treatment, E/e', Post-ANGII6 months post-treatment, E/e', baseline6 months post-treatment, E/e', Post-ANGII
Hydrochlorothiazide + Potassium6.727.067.035.83
Placebo6.556.707.357.48
Spironolactone (MR Blockade)6.677.096.766.28

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Change in Renal Plasma Flow

Renal vasculature was assessed by examining renal plasma flow, or para-aminohippurate (PAH) clearance, basally and in response to acute administration (3 nanograms/kg/min for 60 min) of the vasoactive agent, Angiotensin II. (NCT00865124)
Timeframe: Baseline and six months

,,
InterventionmL/min/1.73m^2 (Mean)
Pre-treatment, PAH clearance, baselinePre-treatment, PAH clearance, Post-ANGII6 months post-treatment, PAH clearance, baseline6 months post-treatment, PAH clearance, Post-ANGII
Hydrochlorothiazide + Potassium508417500415
Placebo518436491427
Spironolactone (MR Blockade)527442518423

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Change in Mitral Annulus Velocities on Tissue Doppler (Delta E/e' Ratio), a Measure of Diastolic Function

Diastolic function was assessed via tissue doppler imaging (TDI) by echocardiography to determine left ventricular diastolic function before and after 6 months of treatment. (NCT00865124)
Timeframe: Baseline and six months

Interventionratio (Mean)
Spironolactone (MR Blockade)0.02
Hydrochlorothiazide + Potassium0.06
Placebo0.64

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Change in Coronary Flow Reserve From Baseline to 6 Months

Coronary flow reserve (CFR), or myocardial perfusion reserve, was assessed via cardiac positron emission tomography (PET). CFR is the ratio of adenosine-stimulated blood flow through myocardium to resting blood flow through myocardium. An improvement in coronary flow reserve is beneficial. (NCT00865124)
Timeframe: Baseline and six months

Interventionratio (Mean)
Spironolactone (MR Blockade)0.33
Hydrochlorothiazide + Potassium-0.10
Placebo0.02

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Change in Sitting Pulse Rate During the Core Phase of the Study

Pulse rate was measured once for 30 seconds just prior to blood pressure measurements in the sitting position. (NCT00867490)
Timeframe: Baseline Phase 2 to end of Phase 2

InterventionBPM (beats per minute) (Mean)
Phase 2 - Aliskiren+HCTZ0.27

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Change in Sitting Pulse Rate During the Extension Phase of the Study

Pulse rate was measured once for 30 seconds just prior to blood pressure measurements in the sitting position. (NCT00867490)
Timeframe: Baseline Phase 3 to end of Phase 3

InterventionBPM (beats per minute) (Mean)
Phase III - Aliskiren+HCTZ+Amlodipine0.03

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Percentage of Patients Who Achieved Normalized Blood Pressure During the Core Phase of the Study

Normalized was defined as a msSBP < 140 mm Hg and/or a msDBP < 90 mm Hg. (NCT00867490)
Timeframe: Baseline Phase 3 to end of Phase 3

InterventionPercentage of patients (Number)
msSBP < 140 mmHgmsDBP < 90 mmHg
Phase III - Aliskiren+HCTZ+Amlodipine54.144.3

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Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Core Phase of the Study

Blood pressure response was defined as msSBP < 140 mmHg or a 20 mmHg decrease in msSBP at the end of Phase 2 compared to Baseline in Phase 2 or a msDBP < 90 mmHg or a 10 mmHg decrease in msDBP at the end of Phase 2 compared to Baseline in Phase 2. (NCT00867490)
Timeframe: Baseline Phase 2 to end of Phase 2

InterventionPercentage of patients (Number)
msSBP responsemsDBP response
Phase 2 - Aliskiren+HCTZ37.434.1

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Extension Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00867490)
Timeframe: Baseline Phase 3 to end of Phase 3

InterventionmmHg (Mean)
Phase III - Aliskiren+HCTZ+Amlodipine-5.87

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Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Core Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00867490)
Timeframe: Baseline Phase 2 to end of Phase 2

InterventionmmHg (Mean)
Phase 2 - Aliskiren+HCTZ-2.81

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Change in Mean Sitting Systolic Blood Pressure (msSBP) During the Extension Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00867490)
Timeframe: Baseline Phase 3 to end of Phase 3

InterventionmmHg (Mean)
Phase III - Aliskiren+HCTZ+Amlodipine-9.20

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Change in Sitting Pulse Pressure During the Core Phase of the Study

Pulse pressure is systolic pressure (SP) minus diastolic pressure (DP). The arm in which the highest sitting DPs were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, SP and DP were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00867490)
Timeframe: Baseline Phase 2 to end of Phase 2

InterventionmmHg (Mean)
Phase 2 - Aliskiren+HCTZ0.31

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Change in Mean Sitting Diastolic Blood Pressure (msDBP) During the Core Phase of the Study

The arm in which the highest sitting diastolic pressures were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, systolic/diastolic blood pressure were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00867490)
Timeframe: Baseline Phase 2 to end of Phase 2

InterventionmmHg (Mean)
Phase 2 - Aliskiren+HCTZ-3.12

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Change in Sitting Pulse Pressure During the Extension Phase of the Study

Pulse pressure is systolic pressure (SP) minus diastolic pressure (DP). The arm in which the highest sitting DPs were found at study entry was the arm used for all subsequent readings. A calibrated sphygmomanometer and appropriate size cuff were used to measure arterial sitting blood pressure (BP) at trough with the arm supported at the level of the heart. At each study visit, after having the patient in a sitting position for at least 5 minutes, SP and DP were measured 3 times at 1-2 minute intervals. A mean was calculated from the 3 measurements. A negative change indicates improvement. (NCT00867490)
Timeframe: Baseline Phase 3 to end of Phase 3

InterventionmmHg (Mean)
Phase III - Aliskiren+HCTZ+Amlodipine-3.33

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Percentage of Patients Who Achieved a Protocol-defined Blood Pressure Response During the Core Phase of the Study

Blood pressure response was defined as msSBP < 140 mmHg or a 20 mmHg decrease in msSBP at the end of Phase 2 compared to Baseline in Phase 2 or a msDBP < 90 mmHg or a 10 mmHg decrease in msDBP at the end of Phase 2 compared to Baseline in Phase 2. (NCT00867490)
Timeframe: Baseline Phase 3 to end of Phase 3

InterventionPercentage of patients (Number)
msSBP responsemsDBP response
Phase III - Aliskiren+HCTZ+Amlodipine54.147.5

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Percentage of Patients Who Achieved Normalized Blood Pressure During the Core Phase of the Study

Normalized blood pressure was defined as a msSBP < 140 mmHg and/or a msDBP < 90 mmHg. (NCT00867490)
Timeframe: Baseline Phase 2 to end of Phase 2

InterventionPercentage of patients (Number)
msSBP < 140 mmHgmsDBP < 90 mmHg
Phase 2 - Aliskiren+HCTZ37.433.3

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Part I: Change in the Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady State in Participants With Impaired Glucose Tolerant (IGT)

Steady state was defined as 90-120 minutes post-dose. The ratio was the quantity of glucose disposed by the body per kg body weight per minute at steady state divided by the approximate steady state plasma insulin concentration. The approximate steady state plasma insulin concentration was estimated by the time-weighted average of the insulin concentration measured at 10 minute intervals in which time = 90, 100, 110, and 120 minutes. IGT was defined as a 2 hour plasma glucose >= 140 and <= 199 mg/dL during a 75g oral glucose tolerance test at screening. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Intervention(mg/kg/minute)/(µIU/mL) (Least Squares Mean)
Hydrochlorothiazide (HCTZ)0.061
Hydrochlorothiazide (HCTZ) Placebo0.045

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Part I: Change in Insulin Secretion at Steady-state Compared to Placebo in Participants Who Had Normal Glucose Tolerance (NGT)

Steady state was defined as 90-120 minutes post-dose. NGT participants (FPG <100 mg/dL & 2 hour plasma glucose (PG) <140 mg/dL during a 75g oral glucose tolerance test (OGTT) at screening) were neither Impaired Glucose Tolerant (IGT) nor Impaired Fasting Glucose (IFG). IGT was defined as a 2 hour plasma glucose >= 140 and <= 199 mg/dL during a 75g oral glucose tolerance test at screening. IFG was defined as FPG between 100 and 125 mg/dL at screening. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Interventionng/minute (Least Squares Mean)
Hydrochlorothiazide (HCTZ)5.54
Hydrochlorothiazide (HCTZ) Placebo5.01

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Part I: Change in Insulin Secretion at Steady-state Compared to Placebo in Participants With Impaired Fasting Glucose (IFG)

Steady state was defined as 90-120 minutes post-dose. IFG was defined as fasting plasma glucose (FPG) between 100 and 125 mg/dL at screening. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Interventionng/minute (Least Squares Mean)
Hydrochlorothiazide (HCTZ)5.60
Hydrochlorothiazide (HCTZ) Placebo4.50

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Part I: Change in Insulin Secretion at Steady-state Compared to Placebo in Participants With Impaired Glucose Tolerance (IGT)

Steady state was defined as 90-120 minutes post-dose. IGT was defined as a 2 hour plasma glucose >= 140 and <= 199 mg/dL during a 75g oral glucose tolerance test at screening. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Interventionng/minute (Least Squares Mean)
Hydrochlorothiazide (HCTZ)3.44
Hydrochlorothiazide (HCTZ) Placebo3.55

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Part I: Change in the Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady State in Participants With Impaired Fasting Glucose (IFG)

Steady state was defined as 90-120 minutes post-dose. The ratio was the quantity of glucose disposed by the body per kg body weight per minute at steady state divided by the approximate steady state plasma insulin concentration. The approximate steady state plasma insulin concentration was estimated by the time-weighted average of the insulin concentration measured at 10 minute intervals in which time = 90, 100, 110, and 120 minutes. IFG was defined as fasting plasma glucose (FPG) between 100 and 125 mg/dL at screening. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Intervention(mg/kg/minute)/(µIU/mL) (Least Squares Mean)
Hydrochlorothiazide (HCTZ)0.038
Hydrochlorothiazide (HCTZ) Placebo0.037

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Part I: Change in the Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady State in Participants With Normal Glucose Tolerant (NGT)

Steady state was defined as 90-120 minutes post-dose. The ratio was the measure of the quantity of glucose disposed per unit of plasma insulin concentration (PIC). Approximate PIC was estimated by the time-weighted average of the insulin concentration measured at 10 minute intervals, time = 90, 100, 110, and 120 minutes. NGT participants (FPG <100 mg/dL & 2 hour PG <140 mg/dL during a 75g OGTT at screening) were neither IGT nor IFG at screening. IGT - defined as a 2 hour PG >= 140 and <= 199 mg/dL during a 75g OGTT at screening. IFG - defined as FPG between 100 and 125 mg/dL at screening. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Intervention(mg/kg/minute)/(µIU/mL) (Least Squares Mean)
Hydrochlorothiazide (HCTZ)0.045
Hydrochlorothiazide (HCTZ) Placebo0.042

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Part II: Ratio of Whole Body Glucose Disposal to Plasma Insulin at Steady-state

Steady state was defined as 90-120 minutes post-dose. The ratio was the quantity of glucose disposed by the body per kg body weight per minute at steady state divided by the approximate steady state plasma insulin concentration. The approximate steady state plasma insulin concentration was estimated by the time-weighted average of the insulin concentration measured at 10 minute intervals in which time = 90, 100, 110, and 120 minutes. (NCT00871871)
Timeframe: 90 -120 minutes post-dose

Intervention(mg/kg/minute)/(µIU/mL) (Least Squares Mean)
Isosorbide Mononitrate (ISMN)0.040
Isosorbide Mononitrate (ISMN) Placebo0.044

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Mean Change From Baseline in Sitting Diastolic Blood Pressure (siDBP) After Adding HCTZ 24 Hours After Morning Dose at Week 6

(NCT00886600)
Timeframe: Baseline and 24-hours after morning dose at Week 6

Interventionmm Hg (Mean)
Placebo / HCTZ 12.5 mg-4.6
Losartan 50 mg q.d. / HCTZ 12.5 mg-9.9
Losartan 100 mg q.d. / HCTZ 12.5 mg-10.7
Losartan 50 mg b.i.d. / HCTZ 12.5 mg-10.1

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Mean Change From Week 4 in Sitting Diastolic Blood Pressure (siDBP) Adding HCTZ 24 Hours After Morning Dose at Week 6

(NCT00886600)
Timeframe: Baseline and 24-hours after morning dose at Week 6

Interventionmm Hg (Mean)
Placebo / HCTZ 12.5 mg-4.0
Losartan 50 mg q.d. / HCTZ 12.5 mg-5.1
Losartan 100 mg q.d. / HCTZ 12.5 mg-4.0
Losartan 50 mg b.i.d. / HCTZ 12.5 mg-4.0

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Mean Change From Baseline in 24-hour Systolic Ambulatory Blood Pressure Monitoring (ABPM) at Week 4

(NCT00886600)
Timeframe: 24-hour period at baseline and Week 4

Interventionmm Hg (Mean)
Placebo / HCTZ 12.5 mg0
Losartan 50 mg q.d. / HCTZ 12.5 mg-9.2
Losartan 100 mg q.d. / HCTZ 12.5 mg-9.9
Losartan 50 mg b.i.d. / HCTZ 12.5 mg-13.2

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Mean Change From Baseline in 24-hour Diastolic Ambulatory Blood Pressure Monitoring (ABPM) at Week 4

(NCT00886600)
Timeframe: 24 hour period at Baseline and Week 4

Interventionmm Hg (Mean)
Placebo / HCTZ 12.5 mg-0.2
Losartan 50 mg q.d. / HCTZ 12.5 mg-5.2
Losartan 100 mg q.d. / HCTZ 12.5 mg-6.4
Losartan 50 mg b.i.d. / HCTZ 12.5 mg-8.5

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Mean Change From Baseline in Sitting Diastolic Blood Pressure (siDBP) 24 Hours After Morning Dose at Week 4

(NCT00886600)
Timeframe: Baseline and 24-hours after morning dose at Week 4

Interventionmm Hg (Mean)
Placebo / HCTZ 12.5 mg-2.1
Losartan 50 mg q.d. / HCTZ 12.5 mg-6.7
Losartan 100 mg q.d. / HCTZ 12.5 mg-9.6
Losartan 50 mg b.i.d. / HCTZ 12.5 mg-8.8

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Change in Total Adiponectin Level After Addition of Trandolapril to HCTZ Compared With Change in Adiponectin After Addition of HCTZ to Trandolapril

"Comparing the change in adiponectin: rand 1 visit4-visit 3 with rand 2 visit 3-2.~This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril." (NCT00887510)
Timeframe: Over the course of 18 weeks

Interventionmcg/ml (Mean)
Thiazide First-1.36
Trandolapril First0.42

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Change in Oral Glucose Tolerance Test (OGTT) Area Under Curve (AUC) After Addition of Trandolapril to Hydrochlorothiazide (HCTZ) Compared With Change in OGTT AUC After Addition of HCTZ to Trandolapril

Comparing the change in OGTT AUC rand 1 visit4-visit 3 with rand 2 visit 3-2. This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril. This is the primary outcome of the study. (NCT00887510)
Timeframe: OGTT AUC measured over 120 minutes after receiving study intervention for 18-24 weeks.

Interventionminutes*mg/dl (Mean)
Thiazide First-472
Trandolapril First1571

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Percentage of Prescribers Who Adhered to European Society of Hypertension/European Society of Cardiology (ESH/ESC) Guidelines 2007

Blood pressure should be reduced to at least below 140/90 mm Hg (systolic/diastolic),and to lower values, if tolerated, in all hypertensive patients. Target blood pressure should be lower than 130/80 mmHg in diabetics and in high or very high risk patients (NCT00890084)
Timeframe: 12 weeks

Interventionpercentage of prescribers (Number)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)47.7

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Percentage of Patients With Blood Pressure < 140/90 mm Hg

% of high risk patients with Blood Pressure < 140/90 mm Hg (NCT00890084)
Timeframe: 12 weeks

InterventionPercentage of participants (Number)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)69.6

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Percentage of Patients With Blood Pressure < 130/80 mm Hg

(NCT00890084)
Timeframe: 12 weeks

InterventionPercentage of participants (Number)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)13.2

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Percentage of Patients in Whom the Prescriber Decide to Further Lower the Blood Pressure to < 130/80 mm Hg

(NCT00890084)
Timeframe: 12 weeks

Interventionpercentage of patients (Number)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)11.7

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Change in Concomitant Antihypertensive Drugs Given at Study Entry

Percentage of patients who had a change in concomitant antihypertensive drugs prescribed at initiation and after 12 weeks. The antihypertensive drugs were changed (which is stopped, titration of dose and started) or not. (NCT00890084)
Timeframe: baseline and 12 weeks

Interventionpercentage of patients (Number)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)13.6

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BP Response Rate (Drop of Systolic BP of 10mmHg or More)

BP response rate (drop of systolic BP of ≥ 10mmHg) after approximately 12 weeks of treatment with telmisartan (alone or in fixed combination with HCTZ) (NCT00890084)
Timeframe: 12 weeks

InterventionPercentage of patients (Number)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)91.85

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Absolute Blood Pressure Decrease

systolic blood pressure (NCT00890084)
Timeframe: baseline and 12 weeks

Interventionmm Hg (Mean)
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)23.2

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Treatment Patterns

Treatment patterns observed at the end of the study as Micardis monotherapy, Micardis Plus 12.5 and Micardis Plus 25 (with or without changes in concomitant antihypertensive medications). (NCT00890084)
Timeframe: 12 weeks

InterventionPercentage of patients (Number)
Telmisartan 40mgTelmisartan 80mgTelmisartan 40/12,5mgTelmisartan 80/12,5mgTelmisartan 80/25mg
Telmisartan or Telmisartan + Hydrochlorothiazide (HCTZ)4.749.43.329.712.6

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Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 in Third Titrated Group (Olmesartan + Hydrochorothiazide + Amlodipine)

Number of patients that achieved a blood pressure goal of less than 130/85 in third titrated group (olmesartan 40 mg + 25 mg hydrochlorothiazide + amlodipine 5 mg). This combination was maintained as long as the participant's blood pressure remained within predefined parameters. If not, participant discontinued for lack of efficacy. (NCT00890591)
Timeframe: 4 - 9 weeks

InterventionParticipants (Number)
Olmesartan + Hydrochlorothiazide + Amlodipine12

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Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 in Second Titrated Group (Olmesartan 40 mg + 25 mg Hydrochlorothiazide)

Number of patients that achieved a blood pressure goal of less than 130/85 in second titrated group (olmesartan 40 mg + 25 mg hydrochlorothiazide). If BP was > or = to 140/90 at 4,8, or 9 wks the participant went to next level of medication for an additional 4-9 weeks. (NCT00890591)
Timeframe: 4 to 9 weeks

InterventionParticipants (Number)
Olmesartan + Hydrochlorothiazide41

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Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 (Olmesartan 20 mg Monotherapy)

Number of patients that achieved a blood pressure (BP) goal of less than 130/85 in the first group (olmesartan monotherapy 20 mg). If BP was > or = to 140/90 at 4,8, or 9 wks the participant went to next level for an additional 4-9 weeks at the next medication level (NCT00890591)
Timeframe: 4 - 9 wks of olmesartan monotherapy

InterventionParticipants (Number)
Olmesartan Monotherapy38

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Number of Patients That Achieved a Blood Pressure Goal of Less Than 130/85 in First Titrated Group (Olmesartan 20 mg + 12.5 mg Hydrochlorothiazide)

Number of patients that achieved a blood pressure goal of less than 130/85 in first titrated group (olmesartan 20 mg + 12.5 mg hydrochlorothiazide)If BP was > or = to 140/90 at 4,8, or 9 wks the participant went to next level of medication for an additional 4-9 weeks (NCT00890591)
Timeframe: 4 to 9 weeks on combination therapy

InterventionParticipants (Number)
Olmesartan + Hydrochlorothiazide33

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Change in Plasma Sodium/Potassium Level Due to Salt-loading

Na/K ratio is a function of kidney function (NCT00896389)
Timeframe: Plasma sodium and potassium measured from blood collected pre and post salt loading

Interventionratio (Mean)
Genotype GGGenotype AGGenotype AA
rs35929607 SNP0.3-0.30.1

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Change in Plasma Renin Activity Due to Salt-loading

Renin is an enzyme that mediates extracellular fluid and regulates blood pressure. Plasma renin activity (PRA) is a measure of the activity of the plasma enzyme renin. PRA is measured in the laboratory by incubating plasma at physiologic temperature in a buffer that facilitates its enzymatic activity. The natural substrate for the enzyme renin is angiotensinogen. Exogenous angiotensinogen is not added to the reaction mixture. This means that, in effect, the PRA results reported are dependent on both renin concentration and the concentration of its substrate in the patient's plasma. Renin cleaves angiotensinogen to produce a decapeptide, angiotensin I, the concentration of which is assayed using liquid chromatography accompanied by tandem mass spectroscopic detection (LC/MS/MS). PRA levels are reported as the amount of angiotensin I generated per unit of time. Change is defined as the post-salt loading values minus the pre-salt loading values (NCT00896389)
Timeframe: Renin was measured from blood collected pre and post salt loading

Interventionng/ml/h (Mean)
Genotype GGGenotype AGGenotype AA
rs35929607 SNP-0.8-0.3-0.4

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Change in Plasma Aldosterone Level Due to Salt-loading

Aldosterone is a hormone that plays a critical role in homeostatic regulation of blood pressure. Change is defined as the post-salt loading values minus the pre-salt loading values (NCT00896389)
Timeframe: Aldosterone was measured from blood collected pre and post salt loading

Interventionng/dL (Mean)
Genotype GGGenotype AGGenotype AA
rs35929607 SNP-7.5-1.2-1.9

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Blood Pressure Change During Salt Loading

"Systolic blood pressure (SBP) and diastolic blood pressure (DBP) were measured every 15 minutes for 4 hours.~Blood pressure change is calculated by the trapezoid method. Essentially we use the average of blood pressure at each pair of time points (for example, DBP 30min + DBP 15min)/2 + (DBP 45min + DBP 30min)/2 + … up to 4 hours.) normalized by baseline SBP/DBP." (NCT00896389)
Timeframe: Every 15 minutes for 4 hours

InterventionmmHg (Mean)
DBP, Genotype GGDBP, Genotype AGDBP, Genotype AASBP, Genotype GGSBP, Genotype AGSBP, Genotype AA
rs35929607 SNP-25.534.623.2-41.462.944.8

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Blood Pressure Change After 7 Days of Low Dose (12.5 mg) of HCTZ

Blood pressure change is defined as SBP or DBP average over the 24 hour period, Day 8 subtracts Day 0. (NCT00896389)
Timeframe: 24-hr Ambulatory blood pressure were measured every hour on day 0 and day 8

InterventionmmHg (Mean)
DBP, Genotype GGDBP, Genotype AGDBP, Genotype AASBP, Genotype GGSBP, Genotype AGSBP, Genotype AA
rs35929607 SNP02.0-1.11.0-0.7-4.2

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Blood Pressure Change After 7 Days of High Dose (25 mg) of HCTZ

Blood pressure change is defined as SBP or DBP average over the 24 hour period, Day 8 subtracts Day 0. (NCT00896389)
Timeframe: 24-hr Ambulatory blood pressure were measured every hour on day 0 and day 8

InterventionmmHg (Mean)
DBP, Genotype GGDBP, Genotype AGDBP, Genotype AASBP, Genotype GGSBP, Genotype AGSBP, Genotype AA
rs35929607 SNP-20.7-1.71-1.3-4.5

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Change in Plasma Sodium/Potassium Level During Low Dose of HCTZ

Na/K ratio is a function of kidney function (NCT00896389)
Timeframe: Plasma sodium and potassium measured from blood collected pre and post salt loading

Interventionratio (Mean)
Genotype GGGenotype AGGenotype AA
rs35929607 SNP01.00.6

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Change in Plasma Sodium/Potassium Level During High Dose of HCTZ

Na/K ratio is a function of kidney function (NCT00896389)
Timeframe: Plasma sodium and potassium measured from blood collected pre and post salt loading

Interventionratio (Mean)
Genotype GGGenotype AGGenotype AA
rs35929607 SNP102.3

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Fasting Glucose Change After 7 Days of High Dose (25mg) of HCTZ

Values on Day 8 subtracts Day 0. (NCT00896389)
Timeframe: Fasting glucose was measured on day 0 and day 8

InterventionmmHg (Mean)
Fasting glucose, GG GenotypeFasting glucose, AG GenotypeFasting glucose, AA Genotype
rs35929607 SNP1.01.02.3

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Fasting Glucose Change After 7 Days of Low Dose (12.5 mg) of HCTZ

Values on Day 8 subtracts Day 0. (NCT00896389)
Timeframe: Fasting glucose was measured on day 0 and day 8

InterventionmmHg (Mean)
Fasting glucose, GG GenotypeFasting glucose, AG GenotypeFasting glucose, AA Genotype
rs35929607 SNP92-0.1

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Change in Absolute Cardiovascular Risk Score

"The absolute cardiovascular risk assessment uses the Framingham Risk Equation to predict risk of a cardiovascular event over the next 5 years. A score of <10% is a low risk, 10 to 15% is a moderate risk, and >15% is a high risk.~A decrease indicates improvement." (NCT00902304)
Timeframe: Baseline and 26 weeks

Interventionpercentage risk score change (Mean)
Usual Care-2.6
Monotherapy (Initial Monotherapy Arm)-3.3
Combination (Initial Combination Therapy Arm)-3.9

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Number of Patients With Major Clinical Endpoints

Major clinical endpoints measured were all-cause mortality and fatal and non-fatal cardiovascular events (e.g. acute myocardial infarction, stroke and heart failure). (NCT00902304)
Timeframe: 26 weeks

,,
Interventionparticipants (Number)
All-cause mortalityNon-fatal cardiovascular events
Combination (Initial Combination Therapy Arm)013
Monotherapy (Initial Monotherapy Arm)16
Usual Care015

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Participants With End Organ Disease at Baseline and Week 26

"A patient was considered to have end organ damage with either of the following: 1) proteinuria (dipstick = 1+ or more or protein/creatinine ratio > 30mg/mol or 24h urine protein > 0.3g); 2) no proteinuria, but presence of microalbuminuria (urine albumin/creatinine ratio 3.6 to 25mg/mol(male) or 3.6 to 35mg/mol (female) detected; 3) no proteinuria or microalbuminuria, but presence of macroalbuminuria (urine albumin/creatinine ratio > 25mg/mol(male) or >35mg/mol (female) detected OR 4) ECG evidence of LVH (Sokolow-Lyon voltage criteria values >= 38mm).~Baseline potential for end organ damage was calculated in all 1562 randomised patients based on the criteria outlined above. If no investigation/data available, assumed no end-organ damage.~It is important to note that given the limited number of ECGs at 26 weeks, between group comparisons should be limited to the two time points (baseline and 26 weeks)." (NCT00902304)
Timeframe: Baseline and week 26

,,
Interventionparticipants (Number)
BaselineWeek 26 (N = 433, 277, 536)
Combination (Initial Combination Therapy Arm)315177
Monotherapy (Initial Monotherapy Arm)14688
Usual Care226157

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Number of Patients With at Least One Adverse Events Attributable to Anti-hypertensive Therapy

The rate of all adverse events by preferred terms as determined by the General Practice investigators to be related to study intervention therapy was reported. Percentage of adverse events was calculated based on the number of participants analyzed. 41 adverse events were not reported as inadequate information was supplied to allow determination of drug treatment at onset. (NCT00902304)
Timeframe: 26 weeks

Interventionparticipants (Number)
Usual Care70
Monotherapy (Initial Monotherapy Arm)70
Combination (Initial Combination Therapy Arm)169

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Percentage of Patients Who Have Achieved Their Pre-specified (Individualized National Heart Foundation of Australia Criteria) Blood Pressure (BP) Target

BP target groups were: <= 125/75mmHg, <= 130/80mmHg and <= 140/90mmHg. The BP target was based on the patient's clinical risk profile as specified by National Heart Foundation of Australia guidelines. (NCT00902304)
Timeframe: 26 weeks

Interventionpercentage of participants (Number)
Usual Care27.4
Monotherapy (Initial Monotherapy Arm)33.0
Combination (Initial Combination Therapy Arm)37.9

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Change in Self-care Behavior Score From Baseline to Week 26

A modified self-care behavior tool (questionnaire) was used to calculate 2 domain scales: maintenance and confidence. Each domain has a standardized score between 0 and 100. Self-care is best represented by maintenance. Confidence is an important process that moderates the relationship between self-care and outcomes. Higher index score suggests better self-care. A score of 70 or greater can be used as the cut-point to judge self-care adequacy. (NCT00902304)
Timeframe: Baseline and week 26

,,
InterventionChange in score (Mean)
Maintenance scoreConfidence score (N = 422, 269, 520)
Combination (Initial Combination Therapy Arm)3.17-0.71
Monotherapy (Initial Monotherapy Arm)2.27-0.72
Usual Care2.590.93

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Number of 'Early Responder' Patients Who Achieve Individualized Blood Pressure Control After 1 or 2 Adjustments

A comparison of the early responders was made based on the blood pressure measurements taken at the week 6 visit window according to gender and guideline targets. The guideline targets were: patients with renal impairment: 125/75 mmHg; patients with end-organ damage/cardiovascular disease: 130/80 mmHg; others: 140/90 mmHg. (NCT00902304)
Timeframe: 26 weeks

,,
InterventionParticipants (Number)
Male patients with a target of <125/75 mmHgMale patients with a target of <130/80 mmHgMale patients with a target of <140/90 mmHgFemale patients with a target of <125/75 mmHgFemale patients with a target of <130/80 mmHgFemale patients with a target of <140/90 mmHg
Combination (Initial Combination Therapy Arm)6344823442
Monotherapy (Initial Monotherapy Arm)314222511
Usual Care3273121618

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Number of Patients With Depression

Patients with depression refers to potential depressive symptoms, not clinically diagnosed depression. The 2 question Arrol screening tool was used to determine if the patient had potential depressive symptoms. The 2 questions are: During the last month have you often been bothered by feeling down, depressed or hopeless? During the past month have you often been bothered by little interest or pleasure in doing things? The presence of potential depressive symptoms was determined by a 'yes' answer to either of these questions. (NCT00902304)
Timeframe: Baseline and week 26

,,
Interventionparticipants (Number)
BaselineWeek 26
Combination (Initial Combination Therapy Arm)185151
Monotherapy (Initial Monotherapy Arm)9678
Usual Care154129

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Change in the EQ-5D Score

The EQ-5D total indexed score (AUS) measures self-reported quality of life with the following 5 dimensions: mobility (range 1,2,3), self-care (range 1,2,3), usual activity (range 1,2,3), pain/discomfort (range 1,2,3) and anxiety/depression (range 1,2,3), where a 1 indicates no problems, a 2 indicates moderate problems, and a 3 indicates severe problems. The range of possible utility scores are between -0.217 (derived from worse responses from all 5 dimensions with severe problems ie 3,3,3,3,3) and 1.000 (no problems for all 5 dimensions) for each dimension. An increase in EQ-5D indexed score (AUS) indicates improvement. (NCT00902304)
Timeframe: Baseline and 26 weeks

Interventionchange in EQ-5D score (Mean)
Usual Care-0.007
Monotherapy (Initial Monotherapy Arm)0.017
Combination (Initial Combination Therapy Arm)0.011

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Change in Mean Sitting Systolic Blood Pressure

The visit window was from 22 to 36 weeks. If more than one blood pressure measure was available within the specified window, then the one closest to the scheduled visit was used for analysis. If no measure was available within this window, then the last recorded BP post-randomization was used for the endpoint. Analysis of covariance model was used with the factors: baseline blood pressure, treatment and blood pressure target group at randomization. (NCT00902304)
Timeframe: Baseline and 26 weeks

InterventionmmHg (Least Squares Mean)
Usual Care-10
Monotherapy (Initial Monotherapy Arm)-11.6
Combination (Initial Combination Therapy Arm)-14.4

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Change in Mean Sitting Diastolic Blood Pressure

The visit window was from 22 to 36 weeks. If more than one blood pressure measure was available within the specified window, then the one closest to the scheduled visit was used for analysis. If no measure was available within this window, then the last recorded BP post-randomization was used for the endpoint. Analysis of covariance model was used with the factors: baseline blood pressure, treatment and blood pressure target group at randomization. (NCT00902304)
Timeframe: Baseline and 26 weeks

InterventionmmHg (Least Squares Mean)
Usual Care-5.45
Monotherapy (Initial Monotherapy Arm)-6.9
Combination (Initial Combination Therapy Arm)-8.29

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Change in Center for Epidemiologic Studies Depression (CES-D) Score From Baseline to Week 26

"The CES-D score was from 0 to 30, with a higher score indicating a higher level of depression.~The categories for the score are: 0 to 9 suggests no depression; 10 to 15 suggests mild depression; 16 to 24 suggests moderate depression; 24 or above suggests severe depression." (NCT00902304)
Timeframe: Baseline and week 26

Interventionchange in CES-D score (Mean)
Usual Care1.03
Monotherapy (Initial Monotherapy Arm)-1.12
Combination (Initial Combination Therapy Arm)1.19

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Change in 24-hour Systolic Blood Pressure Assessed by 24-hour Ambulatory Blood Pressure Measurement.

Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: Baseline (8 weeks) to 16 weeks

Interventionmm Hg (Least Squares Mean)
Olmesartan(OLM) 40 Mg-Amlodipine(AML) 10 mg-1.9
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5-5.1
OLM 40-AML 10-HCTZ 25-6.6

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Change in Seated Diastolic Blood Pressure (SeDBP) of the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg vs. OM/AML 40/10 mg

Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: baseline (8 weeks) to 16 weeks

Interventionmm Hg (Least Squares Mean)
Olmesartan(OLM) 40 Mg-Amlodipine(AML) 10 mg-6.1
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5-7.1
OLM 40-AML 10-HCTZ 25-8.9

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Change in Seated Systolic Blood Pressure (SeSBP) of the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg vs. OM/AML 40/10 mg

Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: baseline (8 weeks) to week 16

Interventionmm Hg (Least Squares Mean)
Olmesartan(OLM) 40 Mg-Amlodipine(AML) 10 mg-6.9
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5-8.6
OLM 40-AML 10-HCTZ 25-10.5

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Change in 24-hour Diastolic Blood Pressure (DBP) Assessed by 24-hour Ambulatory Blood Pressure Measurement (ABPM).

Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: Baseline (8 weeks) to 16 weeks

Interventionmm Hg (Least Squares Mean)
Olmesartan(OLM) 40 Mg-Amlodipine(AML) 10 mg-2.1
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5-4.0
OLM 40-AML 10-HCTZ 25-5.3

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Number of Subjects Achieving Blood Pressure (BP) Goal at Week 16.

Achieving blood pressure goal is defined as seated blood pressure <140/90 mm Hg; 130/80 mm Hg for participants with diabetes and/or other chronic renal and/or chronic cardiovascular disease. Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: baseline (week 8) to week 16

InterventionParticipants (Number)
Olmesartan(OLM) 40 Mg-Amlodipine(AML) 10 mg65
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.579
OLM 40-AML 10-HCTZ 25111

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In Non-responders, the Number of Subject Meeting Their Blood Pressure Goals Associated With the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg.

The number of non-responding participants who achieved their blood pressure goals at the end of Period 4. Achieving blood pressure goal is defined as seated blood pressure <140/90 mm Hg; 130/80 mm Hg for participants with diabetes and/or other chronic renal and/or chronic cardiovascular disease. Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: week 24 to week 32

InterventionParticipants (Number)
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5 (Non-responders)31
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 25 (Non-responders)89

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In Non-responders, the Change in Seated Diastolic Blood Pressure Associated With the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg.

Change in seated diastolic blood pressure from the beginning to the end of Period 4. Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: week 24 to week 32

Interventionmm Hg (Least Squares Mean)
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5 (Non-responders)-6.7
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 25 (Non-responders)-7.9

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In Non-responders, the Change in Seated Systolic Blood Pressure Associated With the Triple Combinations OM/AML/HCTZ 40/10/12.5 and 40/10/25 mg.

Change in seated systolic blood pressure from the beginning to the end of Period 4. Three cuff blood pressure measurements were taken at each visit. (NCT00902538)
Timeframe: week 24 to week 32

Interventionmm Hg (Least Squares Mean)
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5 (Non-responders)-5.5
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 25 (Non-responders)-7.8

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In Non-responders, the Change in 24-hour Systolic Blood Pressure Assessed by 24-hour Ambulatory Blood Pressure Measurement.

In non-responders, the change in 24-hour systolic blood pressure assessed by 24-hour ambulatory blood pressure measurement from the beginning to the end of Period 4. (NCT00902538)
Timeframe: Week 16 to week 32

Interventionmm Hg (Least Squares Mean)
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5-0.4
OLM 40-AML 10-HCTZ 25-4.3

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In Non-responders, the Change in 24-hour Diastolic Blood Pressure Assessed by 24-hour Ambulatory Blood Pressure Measurement.

In non-responders, the change in 24-hour diastolic blood pressure assessed by 24-hour ambulatory blood pressure measurement from the beginning to the end of Period 4. (NCT00902538)
Timeframe: Week 16 to week 32

Interventionmm Hg (Least Squares Mean)
OLM 40-AML 10-Hydrochlorothiazide (HCTZ) 12.5-2.2
OLM 40-AML 10-HCTZ 25-4.4

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Change in WHO-QOL (WHO-Quality Of Life)

"World Health Organization-Quality Of Life (WHO-QOL), change in quality of life was assessed.~Best value=130.0 (highest quality of life), worst value=0.0 (lowest quality of life)" (NCT00904215)
Timeframe: between baseline (visit 1) and after 12 weeks of treatment (visit 3)

InterventionUnits on a scale (Mean)
Micardis/Micardis Plus2.5

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Change in VAS (Visual Analog Scale)

VAS indicates the health status of the patient. Best value=100.0 (best health status), worst value=0.0 (worst health status) (NCT00904215)
Timeframe: between baseline (visit 1) and after 12 weeks of treatment (visit 3)

InterventionUnits on a scale (Mean)
Micardis/Micardis Plus5.9

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Change in SBP (Systolic Blood Pressure)

The change of the mean SBP (NCT00904215)
Timeframe: between baseline (visit 1) and after 12 weeks of treatment (visit 3)

InterventionmmHg (Mean)
Micardis/Micardis Plus-18

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Change in DBP (Diastolic Blood Pressure)

The change of the mean DBP (NCT00904215)
Timeframe: between baseline (visit 1) and after 12 weeks of treatment (visit 3)

InterventionmmHg (Mean)
Micardis/Micardis Plus-10

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Change in Seated Diastolic Blood Pressure (SeDBP).

Baseline blood pressure was defined as the average values obtained at the randomization visit and at the visit prior to randomization (NCT00923091)
Timeframe: Baseline to week 10

Interventionmm HG (Least Squares Mean)
Olmesartan/Amlodipine/Hydrochlorothiazide 20mg/5mg/12.5 mg-22.5
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/12.5mg-22.5
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/25mg-23.0
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/10mg/12.5mg-23.9
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/10mg/25mg-23.8
Olmesartan/Amlodipine 20mg/5mg-20.5
Olmesartan/Amlodipine 40mg/5mg-21.2
Olmesartan/Amlodipine 40mg/10mg-22.1

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Number of Subjects Reaching Blood Pressure Goal From Week 18 to Week 22

Blood pressure treatment goal was defined as blood pressure <140/90 mmHg or <130/80 mmHg for subjects with diabetes, chronic renal disease, or chronic cardiovascular disease. (NCT00923091)
Timeframe: Week 18 to week 22

InterventionParticipants (Number)
Olmesartan/Amlodipine/Hydrochlorothiazide 20mg/5mg/12.5 mg63
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/12.5mg137

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Number of Subjects Reaching Blood Pressure Goal at Week 26

Blood pressure treatment goal was defined as blood pressure <140/90 mmHg or <130/80 mmHg for subjects with diabetes, chronic renal disease, or chronic cardiovascular disease. (NCT00923091)
Timeframe: Week 22 to week 26

InterventionParticipants (Number)
OLM/AML/HCTZ 40/5/12.5mg Nonresponders Randomized to 40/5/12.529
OLM/AML/HCTZ 40/5/12.5mg Nonresponders Randomized to 40/5/2547

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Number of Subjects Reaching Blood Pressure Goal at Week 10

Blood pressure treatment goal was defined as blood pressure <140/90 mmHg or <130/80 mmHg for subjects with diabetes, chronic renal disease, or chronic cardiovascular disease. (NCT00923091)
Timeframe: baseline to week 10

InterventionParticipants (Number)
Olmesartan/Amlodipine/Hydrochlorothiazide 20mg/5mg/12.5 mg177
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/12.5mg176
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/25mg197
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/10mg/12.5mg190
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/10mg/25mg179
Olmesartan/Amlodipine 20mg/5mg144
Olmesartan/Amlodipine 40mg/5mg155
Olmesartan/Amlodipine 40mg/10mg166

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Change in Seated Systolic Blood Pressure From Week 18 to Week 22

(NCT00923091)
Timeframe: Week 18 to week 22

Interventionmm Hg (Least Squares Mean)
Olmesartan/Amlodipine/Hydrochlorothiazide 20mg/5mg/12.5 mg-5.7
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/12.5mg-6.5

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Change in Seated Systolic Blood Pressure (SeDBP).

(NCT00923091)
Timeframe: Baseline to week 10

Interventionmm Hg (Least Squares Mean)
Olmesartan/Amlodipine/Hydrochlorothiazide 20mg/5mg/12.5 mg-33.2
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/12.5mg-33.7
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/25mg-35.3
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/10mg/12.5mg-35.5
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/10mg/25mg-36.2
Olmesartan/Amlodipine 20mg/5mg-29.9
Olmesartan/Amlodipine 40mg/5mg-30.4
Olmesartan/Amlodipine 40mg/10mg-32.8

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Change in Seated Systolic Blood Pressure (SeDBP) During Open-Label Period VI (Titration Effect From OM/AML/HCTZ 40/5/25 to 40/10/25.

(NCT00923091)
Timeframe: Week 26 to week 54

Interventionmm Hg (Mean)
OLM/AML/HCTZ 40/5/25 Titrated to 40/10/25-11.9

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Change in Seated Diastolic Blood Pressure From Week 22 to Week 26

(NCT00923091)
Timeframe: Week 22 to week 26

Interventionmm Hg (Least Squares Mean)
OLM/AML/HCTZ 40/5/12.5mg Nonresponders Randomized to 40/5/12.5-2.7
OLM/AML/HCTZ 40/5/12.5mg Nonresponders Randomized to 40/5/25-3.8

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Change in Seated Diastolic Blood Pressure From Week 18 to Week 22

(NCT00923091)
Timeframe: Week 18 to week 22

Interventionmm Hg (Least Squares Mean)
Olmesartan/Amlodipine/Hydrochlorothiazide 20mg/5mg/12.5 mg-3.3
Olmesartan/Amlodipine/Hydrochlorothiazide 40mg/5mg/12.5mg-4.1

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Change in Seated Systolic Blood Pressure From Week 22 to Week 26

(NCT00923091)
Timeframe: Week 22 to week 26

Interventionmm Hg (Least Squares Mean)
OLM/AML/HCTZ 40/5/12.5mg Nonresponders Randomized to 40/5/12.5-4.5
OLM/AML/HCTZ40/5/12.5mg Nonresponders Randomized to 40/5/25-6.7

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Number of Patients With DBP Control (DBP < 90 mmHg) at Week 5

DBP control is defined as DBP<90 mmHg (NCT00926289)
Timeframe: Week 5 timepoint

Interventionparticipants (Number)
Telmisartan 40/80 mg150
Telmisartan 40/80 mg + HCTZ 12.5/25 mg391

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Number of Patients With DBP Control (DBP < 90 mmHg) at Week 7

DBP control is defined as DBP<90 mmHg (NCT00926289)
Timeframe: Week 7 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg150
Telmisartan 40/80 mg + HCTZ 12.5/25 mg389

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Number of Patients With SBP Control (SBP < 140 mmHg) at Week 3

SBP control is defined as SBP < 140 mmHg (NCT00926289)
Timeframe: Week 3 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg97
Telmisartan 40/80 mg + HCTZ 12.5/25 mg306

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Number of Patients With SBP Control (SBP < 140 mmHg) at Week 5

SBP control is defined as SBP < 140 mmHg (NCT00926289)
Timeframe: Week 5 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg119
Telmisartan 40/80 mg + HCTZ 12.5/25 mg355

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Number of Patients With SBP Control (SBP < 140 mmHg) at Week 7

SBP control is defined as SBP < 140 mmHg. (NCT00926289)
Timeframe: Week 7 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg122
Telmisartan 40/80 mg + HCTZ 12.5/25 mg363

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Number of Patients With Systolic Blood Pressure (SBP) Response at Week 7

SBP response is defined as SBP<140 mmHg or a reduction of >= 15 mmHg (NCT00926289)
Timeframe: Week 7 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg233
Telmisartan 40/80 mg + HCTZ 12.5/25 mg527

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BP Categories at Week 7

"BP categories comprise:~BP optimal (SBP <120 mmHg and DBP <80 mmHg)~BP normal (SBP <130 mmHg and DBP <85 mmHg but not 'optimal')~BP high normal (SBP <140 mmHg and DBP <90 mmHg but not 'normal')~Grade 1 hypertension (SBP <160 mmHg and DBP <100 mmHg but not 'high normal')~Grade 2 hypertension (SBP <180 mmHg and DBP <110 mmHg but not 'Grade 1 hypertension')~Grade 3 hypertension (SBP ≥180 mmHg or DBP ≥110 mmHg)" (NCT00926289)
Timeframe: Week 7 timepoint

,
InterventionParticipants (Number)
BP optimalBP normalBP high normalGrade 1 hypertensionGrade 2 hypertensionGrade 3 hypertension
Telmisartan 40/80 mg636571204422
Telmisartan 40/80 mg + HCTZ 12.5/25 mg441361381865811

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Change From Baseline in Mean Seated Trough Cuff Diastolic Blood Pressure (DBP) to Week 7

The DBP value at baseline was subtracted from the DBP value at Week 7. (NCT00926289)
Timeframe: Baseline and Week 7

InterventionmmHg (Least Squares Mean)
Telmisartan 40/80 mg-15.4
Telmisartan 40/80 mg + HCTZ 12.5/25 mg-18.6

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Change From Baseline in Mean Seated Trough Cuff SBP to Week 3

The SBP value at baseline was subtracted from the SBP value at Week 3. (NCT00926289)
Timeframe: Baseline and Week 3

InterventionmmHg (Least Squares Mean)
Telmisartan 40/80 mg-26.5
Telmisartan 40/80 mg + HCTZ 12.5/25 mg-33.3

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Change From Baseline in Mean Seated Trough Cuff SBP to Week 5

The SBP value at baseline was subtracted from the SBP value at Week 5. (NCT00926289)
Timeframe: Baseline and Week 5

InterventionmmHg (Least Squares Mean)
Telmisartan 40/80 mg-28.6
Telmisartan 40/80 mg + HCTZ 12.5/25 mg-35.8

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Change From Baseline in Mean Seated Trough Cuff Systolic Blood Pressure (SBP) to Week 7

The SBP value at baseline was subtracted from the SBP value at Week 7. (NCT00926289)
Timeframe: Baseline and Week 7

InterventionmmHg (Least Squares Mean)
Telmisartan 40/80 mg-28.5
Telmisartan 40/80 mg + HCTZ 12.5/25 mg-37.0

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Number of Participants With DBP Response at Week 7

DBP response is defined as DBP<90 mmHg or a reduction of >= 10 mmHg (NCT00926289)
Timeframe: Week 7 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg202
Telmisartan 40/80 mg + HCTZ 12.5/25 mg483

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Number of Patients With Blood Pressure (BP) Control at Week 7

BP control is defined as SBP<140 mmHg and DBP < 90 mmHg and is adjusted for baseline SBP (NCT00926289)
Timeframe: Week 7 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg99
Telmisartan 40/80 mg + HCTZ 12.5/25 mg318

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Number of Patients With BP Control at Week 7

BP control is defined as SBP<140 mmHg and DBP < 90 mmHg and is adjusted for baseline DBP (NCT00926289)
Timeframe: Week 7 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg99
Telmisartan 40/80 mg + HCTZ 12.5/25 mg318

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Number of Patients With DBP Control (DBP < 90 mmHg) at Week 3

DBP control is defined as DBP<90 mmHg (NCT00926289)
Timeframe: Week 3 timepoint

InterventionParticipants (Number)
Telmisartan 40/80 mg131
Telmisartan 40/80 mg + HCTZ 12.5/25 mg343

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Change in Mean Sitting Systolic and Diastolic Blood Pressure After 12 Weeks

To compare the change from baseline in MSSBP and MSDBP after 12 weeks of valsartan/amlodipine-based regimen with losartan-based regimen in patients with Stage 2 systolic hypertension. (NCT00931710)
Timeframe: Baseline to week 12

,
InterventionmmHg (Mean)
Baseline MSSBPWeek 12 MSSBPChange in MSSBP from baseline to Week 12Baseline MSDBPWeek 12 MSDBPChange in MSDBP from baseline to Week 12
Losartan/HCTZ168.5134.3-34.297.682.5-15.1
Valsartan/Amlodipine/HCTZ166.8130.8-36.098.682.5-16.1

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Change in Mean Sitting Diastolic Blood Pressure After 6 Weeks

To compare the change from baseline in mean sitting diastolic blood pressure (MSDBP) after 6 weeks of valsartan/amlodipine-based regimen with losartan-based regimen in patients with Stage 2 systolic hypertension. (NCT00931710)
Timeframe: Baseline to Week 6

,
InterventionmmHg (Mean)
BaselineWeek 6Change from Baseline to Week 6
Losartan/HCTZ97.688.5-9.1
Valsartan/Amlodipine/HCTZ98.685.1-13.6

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Cumulative Percentage of Patients Achieving Blood Pressure Control

To compare the percentage of patients achieving blood pressure control (defined as patients achieving MSSBP < 140 mmHg and MSDBP < 90 mmHg) after 3 and 6 weeks of valsartan/amlodipine-based regimen with losartan-based regimen in patients with Stage 2 systolic hypertension. (NCT00931710)
Timeframe: 3 and 6 weeks

,
Interventioncumulative percentage of patients (Number)
Week 3Week 6
Losartan/HCTZ15.347.1
Valsartan/Amlodipine/HCTZ30.561.5

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Cumulative Percentage of Patients With Incidence of Peripheral Edema Before or at the Corresponding Visit

To assess the incidence of peripheral edema occurring with valsartan/amlodipine-based regimen versus losartan-based regimen in patients with Stage 2 systolic hypertension. (NCT00931710)
Timeframe: 3, 6, 9 and 12 weeks

,
Interventioncumulative percentage of patients (Number)
Week 3Week 6Week 9Week 12
Losartan/HCTZ0.80.80.84.5
Valsartan/Amlodipine/HCTZ0.80.81.32.9

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Cumulative Percentage of Treatment Responders

To compare the percentage of treatment responders (defined as patients with MSSBP < 140 mmHg or demonstrating a decrease from baseline of ≥ 20 mmHg) after 3 and 6 weeks of valsartan/amlodipine-based regimen with losartan-based regimen in patients with Stage 2 systolic hypertension. (NCT00931710)
Timeframe: 3 and 6 weeks

,
InterventionCumulative percentage of responders (Number)
Week 3Week 6
Losartan/HCTZ34.371.5
Valsartan/Amlodipine/HCTZ65.387.0

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Change in Mean Sitting Systolic Blood Pressure After 6 Weeks

To compare the change from baseline in mean sitting systolic blood pressure (MSSBP) after 6 weeks of valsartan/amlodipine-based regimen with a losartan-based regimen in patients with Stage 2 systolic hypertension. (NCT00931710)
Timeframe: Baseline to Week 6

,
InterventionmmHg (Mean)
BaselineWeek 6Change from Baseline to Week 6
Losartan/HCTZ168.5142.5-26.0
Valsartan/Amlodipine/HCTZ166.8135.5-31.3

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Percentage of Responders (Defined as Patients With MSSBP < 140 mmHg or a Reduction From Baseline in MSSBP of ≥20 mmHg) During 8 Weeks.

To compare the cumulative percentage of responders (defined as patients with MSSBP <140 mmHg or a decrease from baseline ≥20 mmHg) during 8 weeks of treatment with an aliskiren, amlodipine, and HCTZ treatment regimen versus an aliskiren and amlodipine treatment regimen in minority patients with Stage 2 hypertension. Cumulative refers to achieving a response before or at the corresponding visit. (NCT00942994)
Timeframe: 8 weeks

,
InterventionPercentage of Responders (Number)
Week 2Week 4Week 8
Aliskiren / Amlodipine72.284.791.9
Aliskiren / Amlodipine / HCTZ79.291.192.6

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Percentage of Patients Achieving Blood Pressure Control (Defined as MSSBP < 140 mmHg and MSDBP < 90 mmHg) During 8 Weeks

To evaluate the cumulative percentage of patients achieving Blood Pressure control (defined as patients achieving an MSSBP <140 mmHg and MSDBP <90 mmHg) during 8 weeks of treatment with an aliskiren, amlodipine, and HCTZ treatment regimen versus an aliskiren and amlodipine treatment regimen in minority patients with Stage 2 hypertension. Cumulative refers to achieving BP control before or at the corresponding visit. (NCT00942994)
Timeframe: 8 weeks

,
InterventionPercentage of Participants (Number)
Week 2Week 4Week 8
Aliskiren / Amlodipine40.257.467.9
Aliskiren / Amlodipine / HCTZ50.574.881.7

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Change From Baseline in Mean Sitting Systolic Blood Pressure (MSSBP) at Week 8

To evaluate change from baseline in MSSBP after 8 weeks of treatment with an aliskiren, amlodipine, and HCTZ treatment regimen versus an aliskiren and amlodipine treatment regimen in minority patients with Stage 2 hypertension. (NCT00942994)
Timeframe: Baseline and week 8

,
InterventionmmHg (Mean)
Baseline [N=202, 209]Week 8 [N=197, 209]Change from baseline to week 8 [N=197, 209]
Aliskiren / Amlodipine167.41137.87-29.54
Aliskiren / Amlodipine / HCTZ167.08130.73-36.43

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Change From Baseline in Mean Sitting Systolic Blood Pressure (MSSBP) at Week 2 and Week 4

Primary objective at additional timepoint. (NCT00942994)
Timeframe: Baseline, Week 2 and Week 4

,
InterventionmmHg (Mean)
Baseline [N=202, 209]Week 2 [N=197, 209]Change from baseline to week 2 [N=197, 209]Week 4 [N=197, 209]Change from baseline to week 4 [N=197, 209]
Aliskiren / Amlodipine167.41143.77-23.64140.43-26.98
Aliskiren / Amlodipine / HCTZ167.08138.35-28.81132.42-34.74

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (MSDBP) at Week 8

To evaluate change from baseline in MSDBP after 8 weeks of treatment with an aliskiren, amlodipine, and HCTZ treatment regimen versus an aliskiren and amlodipine treatment regimen in minority patients with Stage 2 hypertension. (NCT00942994)
Timeframe: Baseline and week 8

,
InterventionmmHg (Mean)
Baseline [N=202, 209]Week 8 [N=197, 209]Change from baseline to week 8 [N=197, 209]
Aliskiren / Amlodipine95.2583.17-12.08
Aliskiren / Amlodipine / HCTZ95.2580.10-15.10

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (MSDBP) at Week 2 and Week 4

Secondary objective at additional timepoint. (NCT00942994)
Timeframe: Baseline, Week 2 and Week 4

,
InterventionmmHg (Mean)
Baseline [N=202, 209]Week 2 [N=197, 209]Change from baseline to week 2 [N=197, 209]Week 4 [N=197, 209]Change from baseline to week 4 [N=197, 209]
Aliskiren / Amlodipine95.2586.24-9.0185.35-9.91
Aliskiren / Amlodipine / HCTZ95.2584.26-10.9581.29-13.92

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Area Under the Curve (AUC(0 to Infinity)) of HCTZ

Plasma Area Under the Curve, a measure of drug exposure following dosing (NCT00953680)
Timeframe: 0 to 30 Hours Post Dose

Interventionng*hr/mL (Least Squares Mean)
Losartan-HCTZ Combination Tablet462.08
Losartan Tablet + HCTZ Capsule499.90

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Area Under the Curve (AUC(0 to Infinity)) of Losartan

(NCT00953680)
Timeframe: 0 to 36 Hours Post Dose

Interventionng*hr/mL (Least Squares Mean)
Losartan-HCTZ Combination Tablet1018.1
Losartan Tablet + HCTZ Capsule1024.9

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Peak Plasma Concentration (Cmax) of HCTZ Following Single Dose Administration of Losartan/HCTZ or Losartan and HCTZ

Peak Plasma Concentration (Cmax), or maximal concentration of drug following dosing (NCT00953680)
Timeframe: 30 Hours Post Dose

Interventionng/mL (Least Squares Mean)
Losartan-HCTZ Combination Tablet76.15
Losartan Tablet + HCTZ Capsule81.76

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Peak Plasma Concentration (Cmax) for Losartan

Peak Plasma Concentration (Cmax), or maximal concentration of drug following dosing. (NCT00953680)
Timeframe: 36 Hours Post Dose

Interventionng/mL (Least Squares Mean)
Losartan-HCTZ Combination Tablet532.7
Losartan Tablet + HCTZ Capsule637.9

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Adjusted Mean Change From Baseline in Daytime (0900 to 2100 Hours) Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])

Data after rescue medication was excluded from this analysis. Baseline was defined as the last assessment prior to the start date and time of the first dose of the double-blind study medication. In cases where time of the first dose or time of the assessment was not available, baseline was defined as the last assessment on or prior to the date of the first dose of the double-blind study medication. Measurements were obtained during lead-in, and Week 12 in the double-blind period. (NCT00976495)
Timeframe: From Baseline to Week 12

InterventionmmHg (Mean)
Placebo-1.55
Dapagliflozin 10 mg-5.93
Hydrochlorothiazide 25 mg-6.83

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Adjusted Percent Change From Baseline in Glomerular Filtration Rate (GFR) at Week 12 (Modified Last Observation Carried Forward [MLOCF])

Baseline was defined as the last assessment prior to the start date and time of the first dose of the double-blind study medication. In cases where time of the first dose or time of the assessment was not available, baseline was defined as the last assessment on or prior to the date of the first dose of the double-blind study medication. If no Week 12 measurement was available, the last available post-baseline measurement obtained on or after Day 23 was used regardless of rescue medication. Measurements were obtained during radomization visit, and Week 12 in the double-blind period by a central laboratory. (NCT00976495)
Timeframe: From Baseline to Week 12

Intervention% Change of Baseline GFR (Mean)
Placebo-2.92
Dapagliflozin 10 mg-10.76
Hydrochlorothiazide 25 mg-3.40

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Adjusted Mean Change From Baseline in Nighttime (0100 to 0600 Hours) Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])

Data after rescue medication was excluded from this analysis. Baseline was defined as the last assessment prior to the start date and time of the first dose of the double-blind study medication. In cases where time of the first dose or time of the assessment was not available, baseline was defined as the last assessment on or prior to the date of the first dose of the double-blind study medication. Measurements were obtained during lead-in, and Week 12 in the double-blind period. (NCT00976495)
Timeframe: From Baseline to Week 12

InterventionmmHg (Mean)
Placebo-0.61
Dapagliflozin 10 mg-0.45
Hydrochlorothiazide 25 mg-7.76

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Adjusted Mean Change From Baseline in 24-Hour Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])

Data after rescue medication was excluded from this analysis. Baseline was defined as the last assessment prior to the start date and time of the first dose of the double-blind study medication. In cases where time of the first dose or time of the assessment was not available, baseline was defined as the last assessment on or prior to the date of the first dose of the double-blind study medication. Measurements were obtained during lead-in, and Week 12 in the double-blind period. (NCT00976495)
Timeframe: From Baseline to Week 12

InterventionmmHg (Mean)
Placebo-0.88
Dapagliflozin 10 mg-3.28
Hydrochlorothiazide 25 mg-6.55

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Percentage of Participants With at Least 1 Adverse Event

An adverse event is defined as any untoward medical occurrence in a clinical investigation participant administered a pharmaceutical product without regard to causality. (NCT00996281)
Timeframe: From Week 0 (Day 1) to Week 52.

Interventionpercentage of participants (Number)
Azilsartan Medoxomil and Chlorthalidone78.5
Olmesartan Medoxomil and Hydrochlorothiazide76.4

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Percentage of Participants With Serum Creatinine Elevations Greater Than 50% From Baseline and Greater Than the Upper Limit of Normal (ULN)

Serum creatinine was measured at every visit and evaluated as a laboratory parameter of special interest. The percentage of participants with creatinine increase ≥50% from Baseline and greater than ULN was summarized: - At any visit (includes transient and persistent elevations). - At the Final Visit (includes persistent elevations and participants whose first elevation may have been at the Final Visit). - At least 2 consecutive visits (includes only persistent elevations). (NCT00996281)
Timeframe: Baseline and Week 52

,
Interventionpercentage of participants (Number)
At any postbaseline visitat the Final Visit≥2 consecutive elevations
Azilsartan Medoxomil and Chlorthalidone14.25.95.1
Olmesartan Medoxomil and Hydrochlorothiazide5.81.01.2

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Proportion of Patients Reaching Blood Pressure Control at the End of Follow-up

This variable gives the proportion of patients reaching blood pressure control over time (< 140 mmHg systolic and < 90 mmHg diastolic) (NCT01030458)
Timeframe: 6 months follow-up after randomization

Interventionparticipants (Number)
Amlodipine Plus Valsartan58
Hydrochlorothiazide Plus Bisoprolol40

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Side-effects to Study Medications

(NCT01030458)
Timeframe: 6 months follow-up after randomization

Interventionparticipants (Number)
Amlodipine Plus Valsartan1
Hydrochlorothiazide Plus Bisoprolol1

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Sitting Systolic Blood Pressure on Automated Measurement

Blood pressure is measured by means of validated oscillometric OMRON 705IT recorders (OMRON Healthcare Europe BV, Nieuwegein, Netherlands), after the patient has been seated for 5 minutes in a quiet room, according to the ESC/ESH guidelines. Three consecutive blood pressure readings are obtained and the average of these 3 measurements is used as the primary outcome. (NCT01030458)
Timeframe: 6 months follow-up after randomization

InterventionmmHg (Mean)
Amlodipine Plus Valsartan127.2
Hydrochlorothiazide Plus Bisoprolol134.1

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Time to Blood Pressure Control

The time (in weeks) after randomisation that will be required to reach and maintain the target, defined as a blood pressure below 140 mmHg systolic and 90 mmHg diastolic. (NCT01030458)
Timeframe: 6 months follow-up after randomization

Interventionweeks (Median)
Amlodipine Plus Valsartan12
Hydrochlorothiazide Plus Bisoprolol18

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Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.

The change in sitting trough clinic systolic blood pressure measured at week 12 or final visit relative to baseline. Trough blood pressure is the average of the non-missing values of the 3 serial trough sitting systolic blood pressure measurements. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-42.5
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-44.0
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-37.1

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Change From Baseline in the Mean Diastolic Blood Pressure During Each Hour of the 24-hour Ambulatory Blood Pressure Monitoring.

The change from baseline for each hour interval of the 24-hour ambulatory blood pressure monitoring measured at week 12 or final visit. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The mean consists of the average (arithmetic mean) of measurements collected at each hour. (NCT01033071)
Timeframe: Baseline and Week 12.

,,
InterventionmmHg (Least Squares Mean)
0 to 1 Hour (n=232; n=212; n=237)1 to 2 Hour (n=232; n=214; n=238)2 to 3 Hour (n=232; n=214; n=238)3 to 4 Hour (n=232; n=214; n=238)4 to 5 Hour (n=232; n=214; n=238)5 to 6 Hour (n=232; n=214; n=238)6 to 7 Hour (n=232; n=214; n=238)7 to 8 Hour (n=232; n=214; n=238)8 to 9 Hour (n=232; n=214; n=238)9 to 10 Hour (n=232; n=214; n=238)10 to 11 Hour (n=232; n=214; n=238)11 to 12 Hour (n=232; n=214; n=238)12 to 13 Hour (n=232; n=214; n=238)13 to 14 Hour (n=232; n=214; n=238)14 to 15 Hour (n=232; n=214; n=238)15 to 16 Hour (n=232; n=214; n=238)16 to 17 Hour (n=232; n=214; n=238)17 to 18 Hour (n=231; n=214; n=238)18 to 19 Hour (n=232; n=214; n=238)19 to 20 Hour (n=232; n=214; n=238)20 to 21 Hour (n=232; n=214; n=238)21 to 22 Hour (n=232; n=214; n=238)22 to 23 Hour (n=232; n=214; n=238)23 to 24 Hour (n=232; n=214; n=238)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-18.2-18.8-21.2-20.8-21.7-20.9-20.8-20.5-20.7-21.0-19.7-19.3-19.2-19.6-18.9-17.8-17.2-16.6-17.4-17.8-16.7-17.8-19.5-20.2
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-20.4-20.9-23.4-23.7-23.7-23.6-22.0-21.9-21.5-21.9-20.7-21.2-20.3-19.5-19.7-18.6-16.9-17.1-18.1-18.5-18.4-18.5-19.6-21.0
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-15.2-15.9-17.7-18.2-17.9-19.0-18.0-17.7-17.9-18.3-16.7-17.0-16.0-15.3-15.4-14.5-13.9-13.2-14.3-13.8-13.9-14.7-15.6-16.4

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Change From Baseline in the Mean Systolic Blood Pressure During Each Hour of the 24-hour Ambulatory Blood Pressure Monitoring.

The change from baseline for each hour interval of the 24-hour ambulatory blood pressure monitoring measured at week 12 or final visit. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The mean consists of the average (arithmetic mean) of measurements collected at each hour. (NCT01033071)
Timeframe: Baseline and Week 12.

,,
InterventionmmHg (Least Squares Mean)
0 to 1 Hour (n=232; n=212; n=237)1 to 2 Hour (n=232; n=214; n=238)2 to 3 Hour (n=232; n=214; n=238)3 to 4 Hour (n=232; n=214; n=238)4 to 5 Hour (n=232; n=214; n=238)5 to 6 Hour (n=232; n=214; n=238)6 to 7 Hour (n=232; n=214; n=238)7 to 8 Hour (n=232; n=214; n=238)8 to 9 Hour (n=232; n=214; n=238)9 to 10 Hour (n=232; n=214; n=238)10 to 11 Hour (n=232; n=214; n=238)11 to 12 Hour (n=232; n=214; n=238)12 to 13 Hour (n=232; n=214; n=238)13 to 14 Hour (n=232; n=214; n=238)14 to 15 Hour (n=232; n=214; n=238)15 to 16 Hour (n=232; n=214; n=238)16 to 17 Hour (n=232; n=214; n=238)17 to 18 Hour (n=231; n=214; n=238)18 to 19 Hour (n=232; n=214; n=238)19 to 20 Hour (n=232; n=214; n=238)20 to 21 Hour (n=232; n=214; n=238)21 to 22 Hour (n=232; n=214; n=238)22 to 23 Hour (n=232; n=214; n=238)23 to 24 Hour (n=232; n=214; n=238)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-33.6-33.4-36.7-36.6-36.8-37.2-36.3-37.2-37.3-36.9-36.1-35.2-34.8-34.1-33.4-30.9-29.6-28.5-29.5-29.7-28.2-30.6-32.9-33.1
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-36.2-36.4-39.3-40.3-40.8-41.2-38.6-38.5-38.1-38.0-37.6-38.2-36.2-35.3-35.0-32.9-31.1-30.8-31.9-32.5-31.2-32.8-34.0-35.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-26.8-27.5-30.0-29.6-30.1-31.5-29.8-29.7-30.5-30.8-29.4-29.3-27.7-26.4-26.2-25.3-24.5-23.1-24.3-23.5-23.0-24.6-25.9-26.1

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Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure.

The change in sitting trough clinic diastolic blood pressure measured at each week indicated relative to baseline. Trough blood pressure is the average (arithmetic mean) of the non-missing values of the 3 serial trough sitting systolic blood pressure measurements. (NCT01033071)
Timeframe: Baseline, Week 4, Week 8 and Week 12.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=343; n=330; n=352)Week 8 (n=344; n=330; n=353)Week 12 (n=344; n=330; n=354)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-14.9-17.0-18.8
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-15.8-17.7-20.5
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-11.7-13.9-16.4

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Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.

The change in sitting trough clinic systolic blood pressure measured at each week indicated relative to baseline. Trough blood pressure is the average of the non-missing values of the 3 serial trough sitting systolic blood pressure measurements. (NCT01033071)
Timeframe: Baseline, Week 4 and Week 8.

,,
InterventionmmHg (Least Squares Mean)
Week 4 (n=343; n=330; n=352)Week 8 (n=344; n=330; n=353)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-34.7-39.1
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-36.7-39.4
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-29.7-33.5

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Percent of Participants Who Reached Target Clinic Systolic Blood Pressure of <140 mm Hg and/or Reduction of ≥20 mm Hg From Baseline and Target Clinic Diastolic Blood Pressure of <90 mm Hg and/or Reduction of ≥10 mm Hg From Baseline.

Percentage of participants who achieve both a clinic diastolic and systolic blood pressure response measured at each week indicated, defined as less than 90 mm Hg and/or reduction from baseline of greater than or equal to 10 mm Hg AND less than 140 mm Hg and/or reduction from baseline of greater than or equal to 20 mm Hg. Diastolic and systolic blood pressure is based on the arithmetic mean of the non-missing values of the 3 serial trough sitting blood pressure measurements. (NCT01033071)
Timeframe: Baseline, Week 4, Week 8 and Week 12.

,,
Interventionpercent of participants (Number)
Week 4 (n=343; n=330; n=352)Week 8 (n=344; n=330; n=353)Week 12 (n=344; n=330; n=354)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD81.388.191.3
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD84.887.392.4
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD74.481.084.7

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Percentage of Participants Who Reached Target Clinic Diastolic Blood Pressure of <90 mm Hg and/or Reduction of ≥10 mm Hg From Baseline.

Percentage of participants who achieve a clinic diastolic blood pressure response measured at each week indicated, defined as less than 90 mm Hg and/or reduction from baseline of greater than or equal to 10 mm Hg. Diastolic blood pressure is the arithmetic mean of the non-missing values of the 3 serial trough sitting diastolic blood pressure measurements. (NCT01033071)
Timeframe: Baseline, Week 4, Week 8 and Week 12.

,,
Interventionpercentage of participants (Number)
Week 4 (n=343; n=330; n=352)Week 8 (n=344; n=330; n=353)Week 12 (n=344; n=330; n=354)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD89.290.794.5
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD89.790.995.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD85.287.891.5

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Percentage of Participants Who Reached Target Clinic Systolic Blood Pressure of <140 mm Hg and/or Reduction of ≥20 mm Hg From Baseline.

Percentage of participants who achieve a clinic systolic blood pressure response measured at each week indicated, defined as less than 140 mm Hg and/or reduction from baseline of greater than or equal to 20 mm Hg. Systolic blood pressure is the arithmetic mean of the non-missing values of the 3serial trough sitting systolic blood pressure measurements. (NCT01033071)
Timeframe: Baseline, Week 4, Week 8 and Week 12.

,,
Interventionpercentage of participants (Number)
Week 4 (n=343; n=330; n=352)Week 8 (n=344; n=330; n=353)Week 12 (n=344; n=330; n=354)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD87.893.393.0
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD90.092.494.2
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD79.885.689.3

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Change From Baseline in 24-hour Mean Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in 24-hour mean diastolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-19.4
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-20.7
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-16.2

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Change From Baseline in 24-hour Mean Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in 24-hour mean systolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The 24-hour mean is the average of all measurements recorded for 24 hours after dosing. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-33.9
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-36.3
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-27.5

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Change From Baseline in Mean Daytime (6 AM to 10 PM) Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in daytime (6am to 10pm) mean diastolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of all measurements recorded between the hours of 6 AM (inclusive) and 10 PM (exclusive). (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-20.1
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-21.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-17.0

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Change From Baseline in Mean Daytime (6 AM to 10 PM) Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in daytime (6am to 10pm) mean systolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Daytime mean is the average of all measurements recorded between the hours of 6 AM (inclusive) and 10 PM (exclusive). (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-35.3
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-37.9
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-28.8

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Change From Baseline in Mean Nighttime (12 AM to 6 AM) Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in the mean nighttime (12am to 6am) diastolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Mean nighttime is the average (arithmetic mean) of measurements recorded between the hours of 12 AM (inclusive) and 6 AM (exclusive). (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-17.5
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-18.0
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-14.0

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Change From Baseline in Mean Nighttime (12 AM to 6 AM) Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in the mean nighttime (12am to 6am) systolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Mean nighttime is the average (arithmetic mean) of measurements recorded between the hours of 12 AM (inclusive) and 6 AM (exclusive). (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-29.6
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-31.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-23.9

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Change From Baseline in Mean Trough Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in trough diastolic blood pressure measured at week 12 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Trough is the average of all measurements recorded from 22 to 24 hours after dosing. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-19.8
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-20.2
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-16.0

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Change From Baseline in Mean Trough Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.

The change in trough systolic blood pressure measured at week 12 relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. Trough is the average of all measurements recorded from 22 to 24 hours after dosing. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-32.9
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-34.9
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-25.9

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Change From Baseline in the Mean Diastolic Blood Pressure at 0 to 12 Hours After Dosing by Ambulatory Blood Pressure Monitoring.

The change in the mean 12 hour diastolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The mean consists of the average (arithmetic mean) of measurements. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-20.4
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-22.2
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-17.5

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Change From Baseline in the Mean Systolic Blood Pressure at 0 to 12 Hours After Dosing by Ambulatory Blood Pressure Monitoring.

The change in the mean 12 hour systolic blood pressure measured at week 12 or final visit relative to baseline. Ambulatory blood pressure monitoring measures blood pressure at regular intervals throughout the day and night. The mean consists of the average (arithmetic mean) of measurements. (NCT01033071)
Timeframe: Baseline and Week 12.

InterventionmmHg (Least Squares Mean)
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD-36.2
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD-38.8
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD-29.7

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Systolic Blood Pressure (SBP)

SBP is observed at Week 0 and Week 52. The change of SBP from Week 0 to Week 52 is calculated. (NCT01050062)
Timeframe: Week 0 and Week 52

,,
InterventionmmHg (Mean)
Week 0Week 52Change from Week 0 to Week 52
Combination Tablet AP152.9132.2-20.7
Combination Tablet BP155.4134.7-20.7
Total153.5132.8-20.7

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Incidence of Adverse Events (AEs)

The number of patient with any AEs, patients with drug-related AEs (NCT01050062)
Timeframe: Week 52

,,
InterventionPatients (Number)
patient with any AEspatients with drug-related AEs
Combination Tablet AP221154
Combination Tablet BP7246
Total293200

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Blood Pressure Normalised Rate

The proportion of the patients with normalized blood pressure in 52 weeks on administrative period. Normalized blood pressure is defined less than 140/90 (SBP/DBP) mmHg according to JSH2009 (NCT01050062)
Timeframe: Week 52

Interventionpercentage of participants (Number)
Combination Tablet AP70.7
Combination Tablet BP61.1
Total68.3

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Target Blood Pressure Achievement Rate

The proportion of the patients with target blood pressure in 52 weeks administrative period. Target blood pressure is defined as 'Guidelines for the management of hypertension (JSH2009)': less than 140/90 (SBP/DBP) mmHg for >= 65 years old or cerebrovascular disorder patient; less than 130/80 in diabetes, chronic kidney disease or myocardial infarction patient; less than 130/85 mmHg for others patient. (NCT01050062)
Timeframe: Week 52

InterventionPercentage of patients (Number)
Combination Tablet AP52.9
Combination Tablet BP43.2
Total50.5

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Diastolic Blood Pressure (DBP)

DBP is observed at Week 0 and Week 52. The change of DBP from Week 0 to Week 52 is calculated. (NCT01050062)
Timeframe: Week 0 and Week 52

,,
InterventionmmHg (Mean)
Week 0Week 52Change from Week 0 to Week 52
Combination Tablet AP84.775.2-9.5
Combination Tablet BP84.675.5-9.1
Total84.775.3-9.4

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Change From Baseline on Daytime Average Heart Rate at Week 4

Change from baseline in daytime average heart rate at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. Daytime was defined as 0600 to 2159 hours, inclusive, local time. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionBeats per minute (Least Squares Mean)
Placebo1.58
Ertugliflozin 1 mg-1.80
Ertugliflozin 5 mg1.10
Ertugliflozin 25 mg-1.07
HCTZ 12.5mg-0.06

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Baseline Seated, Triplicate Trough Heart Rate

Trough heart rate was measured using an automated blood pressure device with the participant in a seated position for at least 5 minutes before and while the heart rate measure was obtained. Three measurements of heart rate were taken at least 2-minutes apart. Baseline trough heart rate is calculated as the mean of triplicate (3) trough heart rate measures. (NCT01096667)
Timeframe: Baseline

Interventionbeats per minute (Mean)
Placebo77.07
Ertugliflozin 1 mg78.73
Ertugliflozin 5 mg77.30
Ertugliflozin 25 mg75.63
HCTZ 12.5mg77.97

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Change From Baseline on 24-hour Average SBP at Week 4

Change from baseline on 24-hour average SBP at Week 4 assessed using 24-hour ABPM. In the case of missing data, last observation carried forward (LOCF). (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo0.26
Ertugliflozin 1 mg-2.71
Ertugliflozin 5 mg-3.73
Ertugliflozin 25 mg-3.42
HCTZ 12.5mg-2.95

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Change From Baseline on Nighttime Average DBP at Week 4

Change from baseline on nighttime average DBP at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. Nighttime was defined as 2200 to 0559 hours, inclusive, local time. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo1.02
Ertugliflozin 1 mg-1.48
Ertugliflozin 5 mg-2.52
Ertugliflozin 25 mg-0.84
HCTZ 12.5mg-0.55

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Change From Baseline on Nighttime Average Heart Rate at Week 4

Change from baseline in 24-hour nighttime average heart rate at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. Nighttime was defined as 2200 to 0559 hours, inclusive, local time. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionBeats per minute (Least Squares Mean)
Placebo-0.18
Ertugliflozin 1 mg-0.15
Ertugliflozin 5 mg1.43
Ertugliflozin 25 mg-1.99
HCTZ 12.5mg-1.24

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Change From Baseline on Nighttime Average SBP at Week 4

Change from baseline on nighttime average SBP at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. Nighttime was defined as 2200 to 0559 hours, inclusive, local time. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo-0.29
Ertugliflozin 1 mg-2.48
Ertugliflozin 5 mg-3.47
Ertugliflozin 25 mg-2.31
HCTZ 12.5mg-2.30

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Number of Participants Who Discontinued Study Drug Due to an AE

An adverse event is defined as any untoward medical occurrence in a clinical investigation participant administered a product or medical device; the event need not necessarily have a causal relationship with the treatment or usage. The table below includes all data collected since first dose of study drug. Discontinuation of study drug due to an AE includes temporary and permanent discontinuation of study drug due to an AE. (NCT01096667)
Timeframe: Up to 28 days (treatment period)

InterventionParticipants (Number)
Placebo0
Ertugliflozin 1 mg0
Ertugliflozin 5 mg0
Ertugliflozin 25 mg1
HCTZ 12.5mg0

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Change From Baseline on 24-hour Urinary Glucose Excretion at Week 4

Urinary glucose excetion was corrected for a duration of 24 hours (with appropriate duration of collection defined as >20 hours and <28 hours). In the case of missing data, LOCF. (NCT01096667)
Timeframe: Baseline and Week 4

Interventiongrams/day (Least Squares Mean)
Placebo4.15
Ertugliflozin 1 mg46.33
Ertugliflozin 5 mg64.54
Ertugliflozin 25 mg74.49
HCTZ 12.5mg-0.48

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Number of Participants Who Experienced an Adverse Event (AE)

An adverse event is defined as any untoward medical occurrence in a clinical investigation participant administered a product or medical device; the event need not necessarily have a causal relationship with the treatment or usage. The table below includes all data collected since first dose of study drug. (NCT01096667)
Timeframe: Up to 63 days (including run-in, treatment period, and follow-up)

InterventionParticipants (Number)
Placebo9
Ertugliflozin 1 mg8
Ertugliflozin 5 mg15
Ertugliflozin 25 mg12
HCTZ 12.5mg10

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Baseline 24-hour, Daytime and Nightime Average Diastolic Blood Pressure (DBP)

Baseline 24-hour average DBP was assessed using 24-hour ABPM. Daytime was defined as 0600 to 2159 hours, inclusive, local time. Nighttime was defined as 2200 to 0559 hours, inclusive, local time. (NCT01096667)
Timeframe: up to 24 hours

,,,,
InterventionmmHg (Mean)
24-hrDaytimeNighttime
Ertugliflozin 1 mg78.6781.7772.05
Ertugliflozin 25 mg80.3683.5973.28
Ertugliflozin 5 mg80.1883.4773.05
HCTZ 12.5mg82.6685.8775.76
Placebo81.8985.3274.24

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Baseline 24-hour, Daytime and Nightime Average Heart Rate

Baseline 24-hour average heart rate was assessed using 24-hour ABPM. Daytime was defined as 0600 to 2159 hours, inclusive, local time. Nighttime was defined as 2200 to 0559 hours, inclusive, local time. (NCT01096667)
Timeframe: up to 24 hours

,,,,
Interventionbeats per minute (Mean)
24-hrDaytimeNighttime
Ertugliflozin 1 mg80.7483.7474.44
Ertugliflozin 25 mg79.4182.1873.49
Ertugliflozin 5 mg79.6882.7173.16
HCTZ 12.5mg79.0881.9573.03
Placebo81.1184.4374.05

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Baseline Average Daytime and Nighttime SBP

Daytime was defined as 0600 to 2159 hours, inclusive, local time. Nighttime was defined as 2200 to 0559 hours, inclusive, local time. (NCT01096667)
Timeframe: Daytime: 16 hours; Nighttime: 8 hours

,,,,
InterventionmmHg (Mean)
DaytimeNighttime
Ertugliflozin 1 mg136.85125.15
Ertugliflozin 25 mg139.56127.13
Ertugliflozin 5 mg138.89126.37
HCTZ 12.5mg143.32131.68
Placebo139.95127.54

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Baseline Seated, Triplicate Trough DBP

Trough DBP was measured using an automated blood pressure device with the participant in a seated position for at least 5 minutes before and while the blood pressure measure is obtained. Three measurements of blood pressure were taken at least 2-minutes apart. Baseline trough DBP is calculated as the mean of triplicate (3) trough DBP measures. (NCT01096667)
Timeframe: Baseline

InterventionmmHg (Mean)
Placebo84.89
Ertugliflozin 1 mg83.08
Ertugliflozin 5 mg83.79
Ertugliflozin 25 mg83.89
HCTZ 12.5mg84.72

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Baseline Fasting Plasma Glucose (FPG)

For FPG, blood was drawn after an overnight fast of at least 8 hours (except water). (NCT01096667)
Timeframe: Baseline

Interventionmg/dL (Mean)
Placebo169.47
Ertugliflozin 1 mg158.38
Ertugliflozin 5 mg158.29
Ertugliflozin 25 mg172.03
HCTZ 12.5mg156.87

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Baseline 24-hour Average Urinary Glucose Excretion

Urinary glucose excetion was corrected for a duration of 24 hours (with appropriate duration of collection defined as >20 hours and <28 hours). (NCT01096667)
Timeframe: 24 hours

Interventiongrams/day (Mean)
Placebo13.35
Ertugliflozin 1 mg9.97
Ertugliflozin 5 mg8.04
Ertugliflozin 25 mg17.56
HCTZ 12.5mg6.96

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Change From Baseline in Seated, Triplicate Trough SBP at Week 4

Trough SBP was measured using an automated blood pressure device with the participant in a seated position for at least 5 minutes before and while the blood pressure measure is obtained. Three measurements of blood pressure were taken at least 2-minutes apart. The change from baseline at Week 4 is the difference between the baseline and Week 4 assessments. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo1.24
Ertugliflozin 1 mg-2.77
Ertugliflozin 5 mg-5.92
Ertugliflozin 25 mg-4.96
HCTZ 12.5mg-3.13

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Baseline 24-hour Average Systolic Blood Pressure (SBP)

Baseline 24-hour average SBP was assessed using 24-hour ambulatory blood pressure monitoring (ABPM). (NCT01096667)
Timeframe: 24 hours

InterventionmmHg (Mean)
Placebo136.11
Ertugliflozin 1 mg133.13
Ertugliflozin 5 mg135.08
Ertugliflozin 25 mg135.59
HCTZ 12.5mg139.55

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Change From Baseline on 24-hour Average DBP at Week 4

Change from baseline on 24-hour average DBP at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo0.77
Ertugliflozin 1 mg-1.89
Ertugliflozin 5 mg-2.34
Ertugliflozin 25 mg-1.50
HCTZ 12.5mg-1.42

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Change From Baseline on 24-hour Average Heart Rate at Week 4

Change from baseline in 24-hour average heart rate at Week 4 using 24 hour ABPM. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionBeats per minute (Least Squares Mean)
Placebo1.00
Ertugliflozin 1 mg-1.22
Ertugliflozin 5 mg1.07
Ertugliflozin 25 mg-1.39
HCTZ 12.5mg-0.56

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Change From Baseline in Seated, Triplicate Trough Heart Rate at Week 4

Trough heart rate was measured using an automated blood pressure device with the participant in a seated position for at least 5 minutes before and while the heart rate measure was obtained. Three measurements of heart rate were taken at least 2-minutes apart. The change from baseline at Week 4 is the difference between the baseline and Week 4 assessments. (NCT01096667)
Timeframe: Baseline and Week 4

Interventionbeats per minute (Least Squares Mean)
Placebo2.34
Ertugliflozin 1 mg-1.86
Ertugliflozin 5 mg1.22
Ertugliflozin 25 mg-1.51
HCTZ 12.5mg-0.99

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Change From Baseline in Seated, Triplicate Trough DBP at Week 4

Trough DBP was measured using an automated blood pressure device with the participant in a seated position for at least 5 minutes before and while the blood pressure measure is obtained. Three measurements of blood pressure were taken at least 2-minutes apart. The change from baseline at Week 4 is the difference between the baseline and Week 4 assessments. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo0.30
Ertugliflozin 1 mg-0.90
Ertugliflozin 5 mg-0.75
Ertugliflozin 25 mg-2.71
HCTZ 12.5mg-2.54

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Change From Baseline in FPG at Week 4

For FPG, blood was drawn after an overnight fast of at least 8 hours (except water). (NCT01096667)
Timeframe: Baseline and Week 4

Interventionmg/dL (Least Squares Mean)
Placebo4.39
Ertugliflozin 1 mg-13.70
Ertugliflozin 5 mg-30.41
Ertugliflozin 25 mg-31.03
HCTZ 12.5mg3.79

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Change From Baseline in FPG at Week 2

For FPG, blood was drawn after an overnight fast of at least 8 hours (except water). (NCT01096667)
Timeframe: Baseline and Week 2

Interventionmg/dL (Least Squares Mean)
Placebo-5.44
Ertugliflozin 1 mg-10.98
Ertugliflozin 5 mg-22.45
Ertugliflozin 25 mg-32.03
HCTZ 12.5mg3.21

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Baseline Seated, Triplicate Trough SBP

Trough SBP was measured using an automated blood pressure device with the participant in a seated position for at least 5 minutes before and while the blood pressure measure is obtained. Three measurements of blood pressure were taken at least 2-minutes apart. Baseline trough SBP is calculated as the mean of triplicate (3) trough SBP measures. (NCT01096667)
Timeframe: Baseline

InterventionmmHg (Mean)
Placebo135.17
Ertugliflozin 1 mg134.23
Ertugliflozin 5 mg137.31
Ertugliflozin 25 mg135.25
HCTZ 12.5mg138.07

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Change From Baseline on Daytime Average DBP at Week 4

Change from baseline on daytime average DBP at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. Daytime was defined as 0600 to 2159 hours, inclusive, local time. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo0.87
Ertugliflozin 1 mg-2.12
Ertugliflozin 5 mg-1.88
Ertugliflozin 25 mg-1.77
HCTZ 12.5mg-1.69

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Change From Baseline on Daytime Average SBP at Week 4

Change from baseline on daytime average SBP at Week 4 using 24 hour ABPM. In the case of missing data, LOCF. Daytime was defined as 0600 to 2159 hours, inclusive, local time. (NCT01096667)
Timeframe: Baseline and Week 4

InterventionmmHg (Least Squares Mean)
Placebo0.82
Ertugliflozin 1 mg-2.88
Ertugliflozin 5 mg-3.61
Ertugliflozin 25 mg-4.17
HCTZ 12.5mg-3.10

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Plasma Insulin

A Hyperglycemic clamp was performed once during each study period to assess glucose stimulated insulin secretion. Glucose is infused intravenously to maintain blood glucose near 200 mg/dL to stimulate insulin secretion. During this time plasma insulin levels were measured and the insulin response is reported as the incremental increase over the first 10 minutes of glucose administration. (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

InterventionuU/ml (Mean)
Baseline, HCTZ OnlyHCTZ + ALI 150HCTZ + ALI 300
HCTZ Plus ALI 150 Then ALI 30075.454.875.7

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Plasma Insulin

A Hyperglycemic clamp was performed once during each study period to assess glucose stimulated insulin secretion. Glucose is infused intravenously to maintain blood glucose near 200 mg/dL to stimulate insulin secretion. During this time plasma insulin levels were measured and the insulin response is reported as the incremental increase over the first 10 minutes of glucose administration. (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

InterventionuU/ml (Mean)
Baseline, HCTZ OnlyHCTZ + ALI 150HCTZ + ALI 150 and SPL 25
HCTZ Plus ALI 150 Then ALI 150 and SPL 2550.143.369.1

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Plasma Glucose

Fasting plasma glucose, measured during hyperglycemic clamp (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

Interventionmg/dl (Mean)
Baseline, HCTZ OnlyHCTZ + ALI 150HCTZ + ALI 150 and SPL 25
HCTZ Plus ALI 150 Then ALI 150 and SPL 25106.1105.7102.1

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Plasma Insulin

A Hyperglycemic clamp was performed once during each study period to assess glucose stimulated insulin secretion. Glucose is infused intravenously to maintain blood glucose near 200 mg/dL to stimulate insulin secretion. During this time plasma insulin levels were measured and the insulin response is reported as the incremental increase over the first 10 minutes of glucose administration. (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

InterventionuU/ml (Mean)
Baseline, HCTZ OnlyHCTZ + SPL 25HCTZ + SPL 50
HCTZ Plus SPL 25 Then SPL 5043.553.444.3

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Plasma Glucose

Fasting plasma glucose, measured during hyperglycemic clamp (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

Interventionmg/dl (Mean)
Baseline, HCTZ OnlyHCTZ + ALI 150 and SPL 25HCTZ + SPL 25
HCTZ Plus SPL 25 Then ALI 150 and SPL 25102.2107.2101.7

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Plasma Insulin

A Hyperglycemic clamp was performed once during each study period to assess glucose stimulated insulin secretion. Glucose is infused intravenously to maintain blood glucose near 200 mg/dL to stimulate insulin secretion. During this time plasma insulin levels were measured and the insulin response is reported as the incremental increase over the first 10 minutes of glucose administration. (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

InterventionuU/ml (Mean)
Baseline, HCTZ OnlyHCTZ + ALI 150 and SPL 25HCTZ + SPL 25
HCTZ Plus SPL 25 Then ALI 150 and SPL 25114.099.9113.2

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Plasma Glucose

Fasting plasma glucose, measured during hyperglycemic clamp (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

Interventionmg/dl (Mean)
Baseline, HCTZ OnlyHCTZ + SPL 25HCTZ + SPL 50
HCTZ Plus SPL 25 Then SPL 5096.4104.8105.9

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Plasma Glucose

Fasting plasma glucose, measured during hyperglycemic clamp (NCT01103245)
Timeframe: at the end of each 1 month study period ( 3 times in total)

Interventionmg/dl (Mean)
Baseline, HCTZ OnlyHCTZ + ALI 150HCTZ + ALI 300
HCTZ Plus ALI 150 Then ALI 300108.6119.7111.4

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AUC0-t of Losartan(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)

Bioequivalence based on Losartan AUC0-t. (NCT01149473)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)959.41
Hyzaar® (Reference)939.492

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Cmax of Losartan(Maximum Observed Concentration of Drug Substance in Plasma)

Bioequivalence based on Losartan Cmax. (NCT01149473)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng/mL (Mean)
Losartan/HCTZ (Test)458.29
Hyzaar® (Reference)409.324

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AUC0-inf of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Infinity)

Bioequivalence based on Hydrochlorothiazide AUC0-inf. (NCT01149473)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)943.22
Hyzaar® (Reference)945.592

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AUC0-inf of Losartan(Area Under the Concentration-time Curve From Time Zero to Infinity)

Bioequivalence based on Losartan AUC0-inf. (NCT01149473)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)957.445
Hyzaar® (Reference)956.046

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AUC0-t of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)

Bioequivalence based on Hydrochlorothiazide AUC0-t. (NCT01149473)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)917.034
Hyzaar® (Reference)919.631

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Cmax of Hydrochlorothiazide(Maximum Observed Concentration of Drug Substance in Plasma)

Bioequivalence based on Hydrochlorothiazide Cmax. (NCT01149473)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng/mL (Mean)
Losartan/HCTZ (Test)136.361
Hyzaar® (Reference)132.717

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AUC0-t of Losartan(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)

Bioequivalence based on Losartan AUC0-t. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)866.88
Hyzaar® (Reference)865.00

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Cmax of Hydroclorothiazide(Maximum Observed Concentration of Drug Substance in Plasma)

Bioequivalence based on Hydrochlorothiazide Cmax. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng/mL (Mean)
Losartan/HCTZ (Test)177.63
Hyzaar® (Reference)161.56

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Cmax of Losartan Carboxy Acid(Maximum Observed Concentration of Drug Substance in Plasma)

Informational comparison of Cmax values for the metabolite Losartan Carboxy Acid. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng/mL (Mean)
Losartan/HCTZ (Test)726.85
Hyzaar® (Reference)675.54

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Cmax of Losartan(Maximum Observed Concentration of Drug Substance in Plasma)

Bioequivalence based on Losartan Cmax. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng/mL (Mean)
Losartan/HCTZ (Test)509.63
Hyzaar® (Reference)538.11

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AUC0-inf of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Infinity)

Bioequivalence based on Hydrochlorothiazide AUC0-inf. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)1087.64
Hyzaar® (Reference)1030.73

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AUC0-inf of Losartan(Area Under the Concentration-time Curve From Time Zero to Infinity)

Bioequivalence based on Losartan AUC0-inf. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)880.15
Hyzaar® (Reference)877.99

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AUC0-t of Hydrochlorothiazide(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)

Bioequivalence based on Hydrochlorothiazide AUC0-t. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)1057.58
Hyzaar® (Reference)1001.54

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AUC0-t of Losartan Carboxy Acid(Area Under the Concentration-time Curve From Time Zero to Time of Last Measurable Concentration)

Informational comparison of AUC0-t values for the metabolite Losartan Carboxy Acid. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)4236.78
Hyzaar® (Reference)4117.07

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AUC0-inf of Losartan Carboxy Acid(Area Under the Concentration-time Curve From Time Zero to Infinity)

Informational comparison of AUC0-inf values for the metabolite Losartan Carboxy Acid. (NCT01149486)
Timeframe: Blood samples collected over a 48 hour period.

Interventionng*h/mL (Mean)
Losartan/HCTZ (Test)4281.32
Hyzaar® (Reference)4164.62

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Change From Baseline in Left Ventricular (LV) Function, Left Atrial Volume (Biplane Simpson's Method) in Combination of Aliskiren With Amlodipine

Reductions in the following measurements were analysed between the baseline visit and the final visit: left atrial volume (biplane Simpson's method) (NCT01176032)
Timeframe: Baseline, Week 36

Interventioncm3/m^2 (Mean)
Aliskiren-8.88
Aliskiren + Amlodipinet7.78
Losartan-7.42
Losartan + Amlodipine1.30

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Change From Baseline in Reduction of Left Ventricular Mass Index (LVMI)

Echocardiogram was performed at week 1 and at week 36. Reduction in LVMI is defined as the difference between the LVMI at the final visit and the baseline LVMI (NCT01176032)
Timeframe: Baseline, Week 36

Interventiong/m^2 (Mean)
Aliskiren-8.05
Lostaran-7.96

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Change From Baseline of LVMI in Combination of Aliskiren With Amlodipine

Echocardiogram was performed at week 1 and at week 36. Reduction in LVMI is defined as the difference between the LVMI at the final visit and the baseline LVMI (NCT01176032)
Timeframe: Baseline, Week 36

Interventiong/m2 (Mean)
Aliskiren-5.68
Aliskiren + Amlodipinet-10.26
Losartan-3.59
Losartan + Amlodipine-11.46

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Change From Baseline in Biomarkers in Heart Disease

The plasma level of biomarkers parameters used to measure improvement in left ventricular (LV) function or reduction in left ventricular mass index (LVMI). The following biomarkers were analyzed: cardiotrophin-1 (CT-1), matrix metalloproteinase-1 (MMP-1); tissue inhibitor of MMPs (TIMP-1); annexin A5 (AnxA5); N-terminal prohormone of B-type natriuretic peptide (NT-proBNP) (NCT01176032)
Timeframe: Baseline, Week 36

,
Interventionng/ml (Mean)
cardiotrophin-1 (CT-1) (n=32,37)matrix metalloproteinase-1 (MMP-1) (n=32,37)tissue inhibitor of MMPs (TIMP-1) (n=32,37)annexin A5 (AnxA5) (n=31,37)NT-proBNP (n=31,34)
Aliskiren-169.155.93-0.70-0.9818.66
Lostaran-128.235.519.15-1.21-7.55

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Change From Baseline in Combination of Aliskiren With Amlodipine in Biomarkers of Heart Disease.

The plasma level of biomarkers parameters used to measure improvement in left ventricular (LV) function or reduction in left ventricular mass index (LVMI). The following biomarkers were analyzed: cardiotrophin-1 (CT-1), matrix metalloproteinase-1 (MMP-1); tissue inhibitor of MMPs (TIMP-1); annexin A5 (AnxA5); N-terminal prohormone of B-type natriuretic peptide (NT-proBNP) (NCT01176032)
Timeframe: Baseline, Week 36

,,,
Interventionng/ml (Mean)
CT-1(n=15,17,16,21)ANXA5 (n=15,16,16,21)MMP-1(n=15,17,16,21)TIMP-1 (n=15,17,16,21)NT-proBNP (n=15,16,15,19)
Aliskiren-289.18-1.247.00-10.0121.00
Aliskiren + Amlodipine-63.23-0.744.997.5116.46
Losartan156.89-1.735.4721.38-3.68
Losartan + Amlodipine-345.47-0.815.54-0.16-10.60

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Change From Baseline in Left Ventricular (LV) Function, LV Ejection Fraction (Teicholz), and LV Ejection Fraction (Simpson)

Reductions in the following measurements were analysed between the baseline visit and the final visit: LV ejection fraction (Teicholz), and LV ejection fraction (Simpson) (NCT01176032)
Timeframe: Baseline, Week 36

,
InterventionPercent (Mean)
LV ejection fraction Teicholz(n=29,36)LV ejection fraction Simpson(n=22,34)
Aliskiren0.000.02
Lostaran0.010.00

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Change From Baseline in Left Ventricular (LV) Function, LV End-diastolic Volume by Simpson's Rule, and LV End-systolic Volume by Simpson's Rule

Reductions in the following measurements were analysed between the baseline visit and the final visit: LV end-diastolic volume by Simpson's rule, and LV end-systolic volume by Simpson's rule (NCT01176032)
Timeframe: Baseline, Week 36

,
Interventionml (Mean)
LV end-diastolic volume (n=22,34)LV end-systolic volume (n=22,34)
Aliskiren2.30-0.92
Lostaran0.540.64

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Change From Baseline in Left Ventricular (LV) Function, LV End-diastolic Volume by Simpson's Rule, and LV End-systolic Volume by Simpson's Rule in Combination of Aliskiren With Amlodipine

Reductions in the following measurements were analysed between the baseline visit and the final visit: LV end-diastolic volume by Simpson's rule, and LV end-systolic volume by Simpson's rule (NCT01176032)
Timeframe: Baseline, Week 36

,,,
Interventionml (Mean)
LV end-diastolic volume (n=11,11,15,19)LV end-systolic volume (n=11,11, 15,19)
Aliskiren6.60-2.93
Aliskiren + Amlodipinet-2.001.09
Losartan5.016.11
Losartan + Amlodipine-2.98-3.69

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Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Patients With Satisfactory Response Rate

Response rate was defined as the proportion of patients with a satisfactory systolic BP response (SBP < 140 mmHg or reduction of ≥ 10 mmHg compared to baseline) and a satisfactory diastolic BP response (DBP < 90 mmHg or reduction of ≥ 5 mmHg compared to baseline) (NCT01176032)
Timeframe: Baseline, Week10,18,26,36

,
InterventionPatients (Number)
Baseline, Week 10Baseline, Week 18Baseline, Week 26Baseline, Week 36
Aliskiren16242422
Lostaran15212725

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Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Patients With SBP < 140 mmHg and DBP < 90 mmHg Compared to Baseline

The control rate was defined as the proportion of patients with SBP < 140 mmHg and DBP < 90 mmHg compared to baseline (NCT01176032)
Timeframe: Week10,18,26,36

,
InterventionPatients (Number)
Control rate at Week 10Control rate at Week 18Control rate at Week 26Control rate at Week 36
Aliskiren15202221
Lostaran13192320

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Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Rate of Use of Added Antihypertensive Rescue Drugs

The rate of use of first and second antihypertensive rescue drugs added was also assessed at all visits after week 2. The rescue drug at week 10 and 18 for those patients not achieving the required BP was amlodipine, Patients who did not achieve the required BP at week 26 were treated with hydrochlorothiazide (NCT01176032)
Timeframe: Baseline, Week 10,18,26

,
InterventionPatients (Number)
Baseline, Week 10 (amlodipine)Baseline, Week 18 (amlodipine)Baseline, Week 26 (hydrochlorothiazide)
Aliskiren1122
Lostaran1594

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Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Reduction in Diastolic Blood Pressure (DBP)

The mean systolic BP (SBP) and diastolic BP (DBP) readings for the aliskiren and losartan treatment groups, the difference in these values between the two groups and the comparison of post-baseline vs. baseline values (NCT01176032)
Timeframe: Baseline, Week 10,18,26,36

,
InterventionmmHg (Mean)
Baseline, Week 10 (n=30,37)Baseline, Week 18 (n=29,36)Baseline, Week 26 (n=29,36)Baseline, Week 36 (n=32,37)
Aliskiren-1.77-5.34-5.34-4.19
Lostaran-3.15-7.07-6.94-6.68

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Effectivness of Aliskiren in Controlling Blood Pressure Compare to Losartan in Terms of Reduction in Systolic Blood Pressure (SBP)

The mean systolic BP (SBP) and diastolic BP (DBP) readings for the aliskiren and losartan treatment groups, the difference in these values between the two groups and the comparison of post-baseline vs. baseline values (NCT01176032)
Timeframe: Baseline, Week 10,18,26,36

,
InterventionmmHg (Mean)
Baseline, Week 10 (n=30,37)Baseline, Week 18 (n=29,36)Baseline, Week 26 (n=29,36)Baseline, Week 36 (n=32,37)
Aliskiren-5.56-9.77-12.69-8.87
Lostaran-4.03-8.44-10.40-8.88

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Change From Baseline in Left Ventricular (LV) Function, LV Ejection Fraction (Teicholz), and LV Ejection Fraction (Simpson) in Combination of Aliskiren With Amlodipine

Reductions in the following measurements were analysed between the baseline visit and the final visit: LV ejection fraction (Teicholz), and LV ejection fraction (Simpson) (NCT01176032)
Timeframe: Baseline, Week 36

,,,
InterventionPercent (Mean)
LV ejection fraction Teicholz (n=14,15,16,20)LV ejection fraction Simpson(n=11,11,15,19)
Aliskiren0.000.05
Aliskiren + Amlodipinet-0.00-0.01
Losartan-0.00-0.02
Losartan + Amlodipine0.010.02

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Change From Baseline in Biomarker Such as Aldosterone (Aldo) in Heart Disease

The plasma level of biomarker parameter (aldosterone (Aldo)) used to measure improvement in left ventricular (LV) function or reduction in left ventricular mass index (LVMI) (NCT01176032)
Timeframe: Baseline, Week 36

Interventionng/dl (Mean)
Aliskiren-1.81
Lostaran-7.90

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Change From Baseline in Biomarker Such as Aldosterone (Aldo) in Heart Disease in Combination of Aliskiren With Amlodipine

The plasma level of biomarker parameter plasma aldosterone used to measure improvement in left ventricular (LV) function or reduction in left ventricular mass index (LVMI). (NCT01176032)
Timeframe: Baseline, Week 36

Interventionng/dl (Mean)
Aliskiren2.81
Aliskiren + Amlodipine-5.89
Losartan-3.12
Losartan + Amlodipine-11.55

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Change From Baseline in C-terminal Propeptide of Procollagen Type I (PICP)

PICP is a measure of blood concentration of procollagen I carboxy-terminal propeptide (PICP), a peptide released from the myocardium when procollagen is converted to type I collagen. This biomarker exhibits good specificity and sensitivity for identifying myocardial fibrosis in hypertension. (NCT01176032)
Timeframe: Baseline, Week 36

Interventionug/l (Mean)
Aliskiren-5.22
Lostaran-4.25

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Change From Baseline in Left Ventricular (LV) Function, LA (Left Atrium) Diameter

Reductions in the following measurements were analysed between the baseline visit and the final visit: LA diameter (NCT01176032)
Timeframe: Baseline, Week 36

Interventionmm/m^2 (Mean)
Aliskiren-0.13
Lostaran-0.22

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Change From Baseline in Left Ventricular (LV) Function, LA (Left Atrium) Diameter in Combination of Aliskiren With Amlodipine

Reductions in the following measurements were analysed between the baseline visit and the final visit: LA diameter (NCT01176032)
Timeframe: Baseline, Week 36

Interventionmm/m^2 (Mean)
Aliskiren-0.18
Aliskiren + Amlodipinet-0.07
Losartan-0.19
Losartan + Amlodipine-0.24

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Change From Baseline in Left Ventricular (LV) Function, Left Atrial Volume (Biplane Simpson's Method)

Reductions in the following measurements were analysed between the baseline visit and the final visit: left atrial volume (biplane Simpson's method) (NCT01176032)
Timeframe: Baseline, Week 36

Interventioncm3/m^2 (Mean)
Aliskiren-0.55
Lostaran-2.27

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) and Mean Sitting Diastolic Blood Pressure (msDBP) (Analysis by Maximum Treatment)

Sitting BP measurements were performed at every study visit. A negative change from baseline indicates improvement. (NCT01256411)
Timeframe: Baseline, 12 months

,,,
InterventionmmHg (Mean)
msDBPmsSBP
LCZ606 400 mg/Amlodipine-17.4-28.1
LCZ696 200 mg-16.6-24.1
LCZ696 400 mg-14.2-21.3
LCZ696 400 mg/Amlodipine/HCTZ-16.8-29.0

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) and Mean Sitting Diastolic Blood Pressure (msDBP) (Analysis by Mono or Combination Therapy)

Sitting BP measurements were performed at every study visit. A negative change from baseline indicates improvement. (NCT01256411)
Timeframe: Baseline, 12 months

,
InterventionmmHg (Mean)
msDBPmsSBP
LCZ696 Combination Therapy-17.3-28.2
LCZ696 Monotherapy-15.7-23.0

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Number of Participants With Blood Pressure Control Rate of <140/90 mmHg (Analysis by Maximum Treatment)

Blood pressure (BP) control is defined as BP <140/90 mmHg. (NCT01256411)
Timeframe: Baseline to 12 months

InterventionParticipants (Number)
LCZ696 200 mg114
LCZ696 400 mg62
LCZ606 400 mg/Amlodipine77
LCZ696 400 mg/Amlodipine/HCTZ3

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Number of Participants With Blood Pressure Control Rate of <140/90 mmHg (Analysis by Mono or Combination Therapy)

Blood pressure (BP) control is defined as BP <140/90 mmHg. (NCT01256411)
Timeframe: Baseline to 12 months

InterventionParticipants (Number)
LCZ696 Monotherapy176
LCZ696 Combination Therapy80

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Number of Participants With Adverse Events, Serious Adverse Events, and Deaths (Analysis by Actual Treatment)

Participants were monitored throughout the study for adverse events, serious adverse events and deaths. (NCT01256411)
Timeframe: Baseline to 12 months

,,,,
InterventionParticipants (Number)
Adverse events (serious and non-serious)Seroius adverse eventsDeaths
LCZ606 400 mg/Amlodipine5300
LCZ696 100 mg610
LCZ696 200 mg147100
LCZ696 400 mg7820
LCZ696 400 mg/Amlodipine/HCTZ000

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Number of Participants With Renal Dysfunction in Aliskiren Based Regimen Versus Non-Aliskiren Based Regimen

"The renal dysfunction (composite endpoint) was defined as the first occurrence of either of the following:~End-stage renal disease [ESRD] requiring dialysis or transplantation~Doubling of serum creatinine and reaching an eGFR < 45 ml/min/1.73 m^2." (NCT01259297)
Timeframe: End of study (209 days (median))

,
Interventionparticipants (Number)
ESRD requiring dialysis or transplantationDoubling of creatinine & eGFR<45 ml/min/1.73 m^2
Aliskiren Based Regimen07
Non-Aliskiren Based Regimen01

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Percentage of Participants With Standard Assessment of Global Activities in the Elderly (SAGE) Dimensions (Part II)

"Decline in ability to perform everyday activities independently was measured primarily by using the Standard Assessment of Global Activities in the Elderly (SAGE) scale. The SAGE was comprised of 15 questions, each describing an activity. Patient had to indicate how much difficulty he/she had encountered in performing the activity in the last month. Each question's score ranges from 0 (No difficulty) to 3 (difficulty levels were mild (score = 1), moderate (score =2) and severe (score=3)).~Part II of SAGE included 2 dimensions:~Normal if the scores of all SAGE questions is 0 (i.e., No difficulty)~Mobility Only if scores of both SAGE questions 11 and 12 are 0" (NCT01259297)
Timeframe: End of study (209 days [median])

,
Interventionpercentage of participants (Number)
NormalMobility Only
Aliskiren Based Regimen44.266.8
Non-Aliskiren Based Regimen46.568.6

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)

Mean sitting systolic blood pressure (msSBP) is the average of 2 sitting SBP measurements (2 minutes apart). Since each patient had their final follow-up visit at a different time in the trial, these measurements were classified as falling into the 6 week, 6 month, or 12 month measurement period. All available blood pressures were sorted within these periods and the last value within each time range used for analysis. At each timepoint, a patient must have both baseline and postbaseline values to be included in the analysis. (NCT01259297)
Timeframe: Baseline (BL), 6 week, 6 month and 12 month

,
InterventionmmHg (Least Squares Mean)
change from Baseline to 6 week (n=821,867)change from baseline to 6 month (n=730,775)change from baseline to 12 month (n=397,399)
Aliskiren Based Regimen-11.9-10.1-7.7
Non-Aliskiren Based Regimen-8.02-6.8-5.8

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Change From Baseline to End of Study in Standard Assessment of Global Activities in the Elderly (SAGE) Dimensions (Part I)

"Decline in ability to perform everyday activities independently was measured primarily by using the Standard Assessment of Global Activities in the Elderly (SAGE) scale. The SAGE comprised of 15 questions, each describing an activity. Patient had to indicate how much difficulty he/she had encountered in performing the activity in last month. Each question's score ranges from 0 (No difficulty) to 3 (difficulty levels were mild (score = 1), moderate (score =2) and severe (score=3)). Part I of SAGE included 4 dimensions:~Community Cognition (maximum of scores of questions 1 to 6);~Instrumental Activities of daily Living (IADL) (maximum of scores of questions 7 to 10);~Mobility (maximum of scores of questions 11 and 12);.~Basic Activities of daily Living (ADL) (maximum of scores of questions 13 to 15) Each dimension's total score ranged from 0 to 3. 0=best, 3=worst A negative change in value from baseline means improvement in the ability to perform everyday activities." (NCT01259297)
Timeframe: Baseline, End of study (209 days [median])

,
Interventionunits on a scale (Mean)
Community CognitionInstrumental Activities of daily Living (IADL)MobilityADL
Aliskiren Based Regimen-0.04-0.060.01-0.09
Non-Aliskiren Based Regimen-0.05-0.040.00-0.08

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)

Mean sitting diastolic blood pressure (msDBP) is the average of 2 sitting DBP measurements (2 minutes apart). Since each patient had their final follow-up visit at a different time in the trial, these measurements were classified as falling into the 6 week, 6 month, or 12 month measurement period. All available blood pressures were sorted within these periods and the last value within each time range used for analysis. At each timepoint, a patient must have both baseline and postbaseline values to be included in the analysis. (NCT01259297)
Timeframe: Baseline (BL), 6 week, 6 month and 12 month

,
InterventionmmHg (Least Squares Mean)
change from Baseline to 6 week (n=821,867)change from baseline to 6 month (n=730,775)change from baseline to 12 month (n=397,399)
Aliskiren Based Regimen-5.6-4.9-4.3
Non-Aliskiren Based Regimen-3.6-3.5-3.9

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Number of Participants With Total Mortality in Aliskiren Based Regimen Versus Non-aliskiren Based Regimen

The total mortality endpoint was defined as time to death from any cause. Total mortality analysis used the date of last follow-up including the washout period as the censoring date. (NCT01259297)
Timeframe: End of study (209 days (median))

InterventionParticipants (Number)
Aliskiren Based Regimen5
Non-Aliskiren Based Regimen9

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Number of Participants With Composite Cardiovascular Endpoints in Aliskiren+Amlodipine/HCTZ Group Versus All Placebo Group

The composite CV endpoint is based on the following first adjudicated events: CV death, non-fatal MI,non-fatal stroke, significant heart failure (NCT01259297)
Timeframe: End of study (209 days (median))

Interventionparticipants (Number)
Aliskiren+Amlodipine/HCTZ Group2
Placebo8

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Number of Participants With Composite Cardiovascular Endpoints in Aliskiren Based Regimen Versus Non-Aliskiren Based Regimen

The composite CV endpoint is based on the following first adjudicated events: CV death, non-fatal MI,non-fatal stroke, significant heart failure (NCT01259297)
Timeframe: End of study (209 days (median))

Interventionparticipants (Number)
Aliskiren Based Regimen11
Non-Aliskiren Based Regimen14

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Maximum Measured Concentration of Empa in Plasma (Cmax, ss)

Maximum measured concentration of Empa in plasma (Cmax, ss) at steady state (NCT01276288)
Timeframe: Pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 post-dose on Day 5 with EMPA alone and on Day 9 with EMPA plus diuretic. The Pre-dose values were averaged over Days 1 to 4 with EMPA alone and on Days 7 & 8 with EMPA plus diuretic

Interventionnmol/L (Geometric Mean)
Empagliflozin (Empa)939
Empa+ HCT1030
Empa + TOR949

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Change in Urine pH From Baseline

"Change in urine pH from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

InterventionpH (Mean)
Empagliflozin (Empa)-0.132
Hydrochlorothiazide (HCT)-0.452
Torasemide (TOR)-0.147
Empa+ HCT-0.448
Empa + TOR0.130

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Maximum Measured Concentration of TOR in Plasma (Cmax, ss)

Maximum measured concentration of Empa in plasma (Cmax, ss) at steady state (NCT01276288)
Timeframe: Pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 post-dose on Day 4 with TOR alone and on Day 9 with EMPA plus TOR. The Pre-dose values were averaged over Days 1 to 3 with TOR alone and on Days 7 & 8 with EMPA plus TOR

Interventionng/mL (Geometric Mean)
Torasemide (TOR)710
TOR+ Empa741
TOR Metabolite (TOR-M1)42.6
TOR Metabolite (TOR-M3)8.58
TOR-M1+ Empa43.8
TOR-M3 + Empa8.79

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The Change in Micturition Frequency From the Baseline

For this endpoint the change in total micturition frequency from the baseline was only examined for EMPA where baseline was defined as the day before the first drug administration. (NCT01276288)
Timeframe: Baseline and day 5

Interventionvoids per day (Mean)
Empagliflozin (Empa)1.600

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Number of Subjects With Clinical Relevant Abnormalities in Vital Signs, Clinical Laboratory Tests, 12-lead Resting Electrocardiogram (ECG), Physical Examination and Assessment of Tolerability by the Investigator

"Number of subjects with clinical relevant abnormalities in vital signs (blood pressure, pulse rate), 12-lead resting electrocardiogram (ECG), clinical laboratory tests (haematology, clinical chemistry, urinalysis, and monitoring of fasting plasma glucose), physical examination and assessment of tolerability by the investigator.~New abnormal findings were reported as Adverse Events (AE). Only Alanine aminotransferase normal under system organ class investigations was determined as an existing AE." (NCT01276288)
Timeframe: From first drug administration until up to 14 days after the last drug administration, up to 35 days

Interventionparticipants (Number)
Empagliflozin (Empa)1
Hydrochlorothiazide (HCT)0
Torasemide (TOR)0
Empa+ HCT0
Empa + TOR0

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Changes in Bicarbonate Concentrations of Calcium, Bicarbonate Ions and Base Excess in Capillary or Arterialised Blood From Baseline

"Changes in bicarbonate concentrations of calcium, bicarbonate ions and base excess in capillary or arterialised blood from baseline, where baseline was defined as the last measurement before trial drug administration of each treatment period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

,,,,
Interventionmmol/ L (Mean)
Bicarbonate concentrations of calciumbicarbonate ionsBase excess
Empa + TOR-1.590-0.049-1.450
Empa+ HCT1.860-0.0531.720
Empagliflozin (Empa)-1.090-0.049-1.045
Hydrochlorothiazide (HCT)2.020-0.0431.640
Torasemide (TOR)-0.400-0.041-0.420

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Change in Urinary Excretion in a 24-hour Period of Sodium, Potassium, Magnesium, Chloride, Calcium, Phosphate, Creatinine, Uric Acid, Glucose From Baseline

"Change in urinary excretion in a 24-hour period of sodium, potassium, magnesium, chloride, calcium, phosphate, creatinine, uric acid, glucose from baseline, where baseline was defined as the value obtained from the last 24-hour (h) collection period before the first drug administration in the first treatment period. This applies also to sodium excretion in urine, which is additionally obtained one day before the drug administration before the second period.~The mean change from baseline was evaluated as:~Empa: day 5- baseline, HCT: day 4-baseline, TOR: day 4-baseline, Empa+ HCT: day 9- baseline, Empa+ TOR: day 9- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: 24 hour sampling interval at baseline and then day 5 for Empa, day 4 for TOR and HCT, day 9 for Empa+TOR and Empa+HCT

,,,,
Interventionmmol/day (Mean)
SodiumChloridePotassiumMagnesiumCalciumPhosphateCreatinineUric acidGlucose
Empa + TOR1.200-14.6008.4601.050-0.7405.000-0.0401.244740.910
Empa+ HCT28.90011.40015.7902.030-1.3608.3000.0221.555685.233
Empagliflozin (Empa)-4.300-16.30010.3701.190-1.1609.2500.0911.641599.449
Hydrochlorothiazide (HCT)-11.700-12.3006.2002.270-1.0209.000-0.078-0.03717.584
Torasemide (TOR)-13.700-22.000-6.9901.720-0.4304.900-0.073-0.50017.932

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Change in Serum Concentration of Sodium, Potassium, Magnesium, Calcium, Chloride, Phosphate, Glucose and Urea From Baseline

"Change in serum concentration of sodium, potassium, magnesium, calcium, chloride, phosphate, glucose and urea from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

,,,,
Interventionmmol/L (Mean)
SodiumPotassiumMagnesiumChlorideCalciumPhosphateUreaGlucose
Empa + TOR1.600-0.3600.1452.100-0.0600.0502.122-0.526
Empa+ HCT-0.100-0.5300.130-3.200-0.0100.1701.504-0.033
Empagliflozin (Empa)1.500-0.1700.1392.050-0.0550.0450.710-1.123
Hydrochlorothiazide (HCT)-0.500-0.4700.025-2.600-0.0400.0600.6500.849
Torasemide (TOR)0.200-0.2000.0591.000-0.080-0.0600.3180.527

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The Change in Total Muscle Sympathetic Nerve Activity (MSNA) From Off- Treatment

The change in total Muscle sympathetic nerve activity (MSNA) that represents an area under the curve of all C-fiber action potentials per minute. This endpoint was evaluated only for Empa. For this endpoint a baseline value was not defined. However, the parameters obtained at 2 measurements time points during the trial were compared. (NCT01276288)
Timeframe: One day before the drug administration, then day 4 after the first drug administration

Interventionaction potentials per min (Mean)
Empagliflozin (Empa)0.241

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Change in Clearance of Sodium, Potassium, Creatinine, Magnesium, Chloride,Calcium, Phosphate and Uric Acid From Baseline

"Change in clearance of sodium, potassium, creatinine, magnesium, chloride,calcium, phosphate and uric acid from baseline, where baseline is defined as the value obtained from the last 24-h collection period before the first drug administration in the first treatment period.~The mean change from baseline was evaluated as:~Empa: day 5- baseline, HCT: day 4-baseline, TOR: day 4-baseline, Empa+ HCT: day 9- baseline, Empa+ TOR: day 9- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: 24 hour sampling interval at baseline and then day 5 for Empa, day 4 for TOR and HCT, day 9 for Empa+TOR and Empa+HCT

,,,,
Interventionml/min (Mean)
SodiumChloridePotassiumMagnesiumCalciumPhosphateUric AcidCreatinine
Empa + TOR-0.004-0.1172.3240.209-0.1742.3594.359-11.768
Empa+ HCT0.1430.1144.1251.115-0.4072.7955.065-10.126
Empagliflozin (Empa)-0.031-0.1292.0400.398-0.3265.2756.3773.167
Hydrochlorothiazide (HCT)-0.055-0.0582.2051.826-0.2994.633-0.476-7.034
Torasemide (TOR)-0.071-0.157-0.5181.148-0.0654.368-1.310-4.250

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Change in pH in Capillary or Arterialised Blood From Baseline

"Change in pH in capillary or arterialised blood from baseline, where baseline was defined as the last measurement before trial drug administration of each treatment period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

InterventionpH (Mean)
Empagliflozin (Empa)-0.006
Hydrochlorothiazide (HCT)0.003
Torasemide (TOR)-0.002
Empa+ HCT0.008
Empa + TOR-0.005

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Maximum Measured Concentration of HCT in Plasma (Cmax, ss)

Maximum measured concentration of HCT in plasma (Cmax, ss) at steady state (NCT01276288)
Timeframe: Pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 post-dose on Day 4 with HCT alone and on Day 9 with EMPA plus HCT. The Pre-dose values were averaged over Days 1 to 3 with HCT alone and on Days 7 & 8 with EMPA plus HCT

Interventionng/mL (Geometric Mean)
Hydrochlorothiazide (HCT)203
HCT+ Empa205

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Urinary Sodium Excretion Over 24-hour run-in Periods

Urinary sodium excretion over 24-hour run-in periods to assess the harmonisation of electrolytes after intake of a standardised diet (NCT01276288)
Timeframe: Day 3, 2 and 1 before the first drug administration

,,
Interventionmmol/day (Mean)
3 days before the drug administration2 days before the drug administration1 day before the drug administration
Empagliflozin (Empa)198.50174.35163.90
Hydrochlorothiazide (HCT)211.10183.30170.10
Torasemide (TOR)217.90178.70179.10

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Change in Urinary Excretion in a 24-hour Period of N-terminal Telopeptide (NTx) From Baseline

"Change in urinary excretion in a 24-hour period of N-terminal telopeptide (NTx) from baseline, where baseline was defined as the value obtained from the last 24-hour (h) collection period before the first drug administration in the first treatment period.~The mean change from baseline was evaluated as:~Empa: day 5- baseline, HCT: day 4-baseline, TOR: day 4-baseline, Empa+ HCT: day 9- baseline, Empa+ TOR: day 9- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: 24 hour sampling interval at baseline and then day 5 for Empa, day 4 for TOR and HCT, day 9 for Empa+TOR and Empa+HCT

InterventionnM BCE/ mMC (Mean)
Empagliflozin (Empa)6.010
Hydrochlorothiazide (HCT)0.730
Torasemide (TOR)2.030
Empa+ HCT1.380
Empa + TOR3.900

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Change in Urinary Weight From Baseline

"Change from baseline in urinary weight in a 24 hour (h)- collection period, where baseline is the last 24-h collection period before first trial drug administration in each treatment period.~The mean change from baseline was evaluated as:~Empa: day 5- baseline, HCT: day 4-baseline, TOR: day 4-baseline, Empa+ HCT: day 9- baseline, Empa+ TOR: day 9- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: 24 hour sampling interval at baseline and then day 5 for Empa, day 4 for TOR and HCT, day 9 for Empa+TOR and Empa+HCT

Interventiong/day (Mean)
Empagliflozin (Empa)134.700
Hydrochlorothiazide (HCT)-55.300
Torasemide (TOR)-39.000
Empa+ HCT429.000
Empa + TOR353.200

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Change in Urine Osmolality From Baseline

"Change in urine osmolality from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

InterventionmOsm/kg (Mean)
Empagliflozin (Empa)223.15
Hydrochlorothiazide (HCT)-3.900
Torasemide (TOR)-5.800
Empa+ HCT217.700
Empa + TOR330.400

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Change in Serum Concentration of Renin, Intact Parathyroid Hormone (iPTH) and 1,25-dihydroxyvitamin D From Baseline

"Change in serum concentration of Renin, intact parathyroid hormone (iPTH) and 1,25-dihydroxyvitamin D from baseline , where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

,,,,
Interventionpg/mL (Mean)
ReniniPTH1,25-dihydroxyvitamin D
Empa + TOR17.05012.190-0.970
Empa+ HCT32.7609.280-5.060
Empagliflozin (Empa)-0.9608.2650.230
Hydrochlorothiazide (HCT)16.1506.1601.560
Torasemide (TOR)2.5506.9103.530

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Change in Serum Concentration of Creatinine and Uric Acid From Baseline

"Change in serum concentration of Creatinine and Uric acid from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 5- baseline, HCT: day 4-baseline, TOR: day 4-baseline, Empa+ HCT: day 9- baseline, Empa+ TOR: day 9- baseline,~The means for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 5 for Empa, day 4 for TOR and HCT, day 9 for Empa+TOR and Empa+HCT

,,,,
Interventionumol/L (Mean)
CreatinineUric acid
Empa + TOR3.570-48.200
Empa+ HCT6.280-31.000
Empagliflozin (Empa)2.175-64.950
Hydrochlorothiazide (HCT)-0.34024.200
Torasemide (TOR)-2.180-4.700

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Change in Urea Concentration in Urine

"Change in urea concentration in urine from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

Interventionmmol/L (Mean)
Empagliflozin (Empa)-1.515
Hydrochlorothiazide (HCT)67.570
Torasemide (TOR)35.710
Empa+ HCT11.780
Empa + TOR48.690

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Change in Serum Osmolality From Baseline

"Changes in serum osmolality from baseline based on a blood sample.~Baseline was defined as the measurement obtained before the first drug administration in the first period.~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

InterventionmOsm/Kg (Mean)
Empagliflozin (Empa)3.950
Hydrochlorothiazide (HCT)-7.500
Torasemide (TOR)-5.500
Empa+ HCT-2.200
Empa + TOR10.500

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Change in Serum Concentration of Fibroblast Growth Factor-23 (FGF- 23) From Baseline

"Change in serum concentration of fibroblast growth factor-23 (FGF- 23) from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline, The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

InterventionRU/mL (Mean)
Empagliflozin (Empa)50.305
Hydrochlorothiazide (HCT)29.050
Torasemide (TOR)-0.680
Empa+ HCT109.860
Empa + TOR13.820

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Change in Serum Concentration of Alkaline Phosphatase (ALP) From Baseline

"Change in serum concentration of ALP from baseline, where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

InterventionU/L (Mean)
Empagliflozin (Empa)2.750
Hydrochlorothiazide (HCT)3.000
Torasemide (TOR)2.400
Empa+ HCT6.500
Empa + TOR5.800

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Change in Serum Concentration of Aldosterone From Baseline

"Change in serum concentration of Aldosterone from baseline , where baseline was defined as the measurement obtained before first drug administration in the first period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

Interventionnmol/L (Mean)
Empagliflozin (Empa)-0.018
Hydrochlorothiazide (HCT)0.099
Torasemide (TOR)0.023
Empa+ HCT0.124
Empa + TOR0.123

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Change in Body Weight From Baseline

"Change in body weight from baseline , where baseline was defined as the last measurement before trial drug administration of each treatment period~The mean change from baseline was evaluated as:~Empa: day 6- baseline, HCT: day 5-baseline, TOR: day 5-baseline, Empa+ HCT: day 10- baseline, Empa+ TOR: day 10- baseline,~The mean for the Empa arm represent combined adjusted means of all four sequences that is Empa administered before or after the administration of either TOR, HCT and their combination with Empa" (NCT01276288)
Timeframe: baseline and then day 6 for Empa, day 5 for TOR and HCT, day 10 for Empa+TOR and Empa+HCT

Interventionkg (Mean)
Empagliflozin (Empa)-1.365
Hydrochlorothiazide (HCT)-1.040
Torasemide (TOR)-0.380
Empa+ HCT-2.030
Empa + TOR-1.750

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Area Under the Concentration-time Curve of TOR in Plasma (AUCτ,ss)

Area under the concentration-time curve of TOR in plasma at steady state over a uniform dosing interval τ (AUCτ,ss). (NCT01276288)
Timeframe: Pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 post-dose on Day 4 with TOR alone and on Day 9 with EMPA plus TOR. The Pre-dose values were averaged over Days 1 to 3 with TOR alone and on Days 7 & 8 with EMPA plus TOR

Interventionng*h/mL (Geometric Mean)
Torasemide (TOR)1320
TOR+ Empa1340
TOR Metabolite (TOR-M1)74.8
TOR Metabolite (TOR-M3)40.5
TOR-M1+ Empa78.1
TOR-M3 + Empa41.8

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Area Under the Concentration-time Curve of HCT in Plasma (AUCτ,ss)

Area under the concentration-time curve of HCT in plasma at steady state over a uniform dosing interval τ (AUCτ,ss). (NCT01276288)
Timeframe: Pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 post-dose on Day 4 with HCT alone and on Day 9 with EMPA plus HCT. The Pre-dose values were averaged over Days 1 to 3 with HCT alone and on Days 7 & 8 with EMPA plus HCT

Interventionng*h/mL (Geometric Mean)
Hydrochlorothiazide (HCT)1040
HCT+ Empa1000

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Area Under the Concentration-time Curve of Empa in Plasma (AUCτ,ss)

Area under the concentration-time curve of Empa in plasma at steady state over a uniform dosing interval τ (AUCτ,ss). (NCT01276288)
Timeframe: Pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 post-dose on Day 5 with EMPA alone and on Day 9 with EMPA plus diuretic. The Pre-dose values were averaged over Days 1 to 4 with EMPA alone and on Days 7 & 8 with EMPA plus diuretic

Interventionnmol*h/L (Geometric Mean)
Empagliflozin (Empa)4990
Empa+ HCT5570
Empa + TOR5260

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Percentage of Participants Who Experience ≥1 Adverse Event (AE)

An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE. The percentage of participants who experienced at least 1 AE during the 10-week treatment and follow-up period were summarized by study drug received. (NCT01302691)
Timeframe: up to 14 days after last dose of study drug (up to 10 weeks)

InterventionPercentage of Participants (Number)
L50/H12.5/A530.5
L50 + A528.8

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Change in Mean Trough Sitting Diastolic Blood Pressure (SiDBP)

Sitting diastolic blood pressure was measured by automated sphygmomanometer pre-dose on Day 1 (baseline) and at 24 ± 2 hours after the last study drug administration at Week 8. The difference between the baseline and Week 8 assessments was calculated and summarized by treatment arm. (NCT01302691)
Timeframe: Baseline and Week 8

InterventionmmHg (Least Squares Mean)
L50/H12.5/A5-9.1
L50 + A5-8.0

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Percentage of Participants Who Had Study Drug Stopped Due to an AE

An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE. The percentage of participants who had study drug stopped during the 8-week treatment period due to an AE regardless of whether or not they completed the study was summarized by treatment arm (NCT01302691)
Timeframe: up to 8 weeks

InterventionPercentage of Participants (Number)
L50/H12.5/A51.2
L50 + A50.0

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Percentage of Participants Who Experience ≥1 Serious Adverse Event (SAE)

An SAE is any AE occurring at any dose or during any use of Sponsor's product that does the following: results in death; is life threatening; results in persistent or significant disability/incapacity; results in or prolongs an existing inpatient hospitalization; is a congenital anomaly/birth defect; is a cancer; is associated with an overdose; is another important medical event. The percentage of participants who experienced at least 1 SAE during the 10-week treatment and follow-up period were summarized by study drug received. (NCT01302691)
Timeframe: up to 14 days after last dose of study drug (up to 10 weeks)

InterventionPercentage of Participants (Number)
L50/H12.5/A50.6
L50 + A50.6

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Change in Mean Trough Sitting Systolic Blood Pressure (SiSBP)

Sitting systolic blood pressure was measured by automated sphygmomanometer pre-dose on Day 1 (baseline) and at 24 ± 2 hours after the last study drug administration at Week 8. The difference between the baseline and Week 8 assessments was calculated and summarized by treatment arm. (NCT01302691)
Timeframe: Baseline and Week 8

InterventionmmHg (Least Squares Mean)
L50/H12.5/A5-13.4
L50 + A5-10.2

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Number of Participants With Adverse Events, Serious Adverse Events and Death as Assessment of Safety and Tolerability of Aliskiren Added to Ramipril

(NCT01302899)
Timeframe: 26 weeks

,,,
InterventionParticipants (Number)
patients with adverse eventspatients with serious adverse eventspatients with death
Ramipril400
Ramipril +HCTZ700
Ramipril+Aliskiren300
Ramipril+Aliskiren + HCTZ500

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Percentage of Participants at Final Visit Who Achieved Both a Clinic Systolic and Diastolic Blood Pressure Response

Systolic/diastolic blood pressure is the arithmetic mean of the 3 serial sitting systolic/diastolic blood pressure measurements. Percentage of participants who achieved both a sitting clinic systolic and diastolic blood pressure response, defined as systolic blood pressure less than 130 mm Hg and diastolic blood pressure less than 80 mm Hg at Week 52. (NCT01309828)
Timeframe: Week 52

Interventionpercentage of participants (Number)
Azilsartan Medoxomil + Chlorthalidone58.7
Olmesartan Medoxomil + Hydrochlorothiazide73.0

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Percentage of Participants at Final Visit Who Achieve Target Systolic Blood Pressure <130 mm Hg

Systolic blood pressure is the arithmetic mean of the 3 serial sitting systolic blood pressure measurements. Percentage of participants who achieve a sitting clinic systolic blood pressure response defined as less than 130 mm Hg at Week 52. (NCT01309828)
Timeframe: Week 52

Interventionpercentage of participants (Number)
Azilsartan Medoxomil + Chlorthalidone69.3
Olmesartan Medoxomil + Hydrochlorothiazide78.4

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Number of Participants With at Least 1 Adverse Event (AE)

An AE is any untoward medical occurrence in a clinical investigation participant administered a drug; it does not necessarily have a causal relationship with this treatment. A serious AE is defined as any untoward medical occurrence that resulted in death, was life threatening, required or prolonged inpatient hospitalization, resulted in persistent or significant disability or incapacity, led to a congenital anomaly/birth defect or was an important medical event that may have required intervention to prevent any of items above. (NCT01309828)
Timeframe: From the first dose of open-label study drug until 14 days (or 30 days for a serious adverse event) after the last dose of open- label study drug (up to 56 weeks).

,
Interventionparticipants (Number)
Adverse EventsAdverse Events Leading to DiscontinuationSerious Adverse EventsSerious Adverse Events Leading to DiscontinuationDeath
Azilsartan Medoxomil + Chlorthalidone6817850
Olmesartan Medoxomil + Hydrochlorothiazide5815941

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Percentage of Participants at Final Visit Who Achieved Target Diastolic Blood Pressure <80 mm Hg

Diastolic blood pressure is the arithmetic mean of the 3 serial sitting diastolic blood pressure measurements. Percentage of participants at Week 52 who achieved a sitting clinic diastolic blood pressure response, defined as less than 80 mm Hg. (NCT01309828)
Timeframe: Week 52

Interventionpercentage of participants (Number)
Azilsartan Medoxomil + Chlorthalidone80.0
Olmesartan Medoxomil + Hydrochlorothiazide87.8

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (MsDBP) at End Point (Week 78 or Last Observation Carried Forward (LOCF)

Sitting blood pressure was measured using a calibrated standard sphygmomanometer after the participants remained in sitting position for 5 minutes at clinic during the visit. The repeat sitting measurements were made at 2 to 3 minute intervals and the mean of three sDBP measurements were used as the average sitting office blood pressure for that visit. (NCT01365481)
Timeframe: Baseline, End Point (Week 78 or Last observation carried forward (LOCF)

Interventionmillimeter(s) of mercury (mmHg) (Mean)
Valsartan + Antihypertensive Group-10.3
Valsartan Alone-10.8

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Number of Participants With MSSBP, MSDBP and (MSSBP and MSDBP Combined) < 95th Percentile for Gender, Age, and Height

Number of Participants with Mean sitting systolic (MSSBP) and mean sitting diastolic(MSDBP) blood pressure and both combined less than the 95th percentile for age, gender and height (NCT01365481)
Timeframe: End Point (Week 78 or Last observation carried forward (LOCF)

,
InterventionNumber of Participants (Number)
MSSBP (n=39, 105)MSDBP (n=28, 51)MSSBP and MSDBP combined (n=40, 105)
Valsartan + Antihypertensive Group232022
Valsartan Alone904788

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP) at End Point (Week 78 or Last Observation Carried Forward (LOCF)

Sitting blood pressure was measured using a calibrated standard sphygmomanometer after the participants remained in sitting position for 5 minutes at clinic during the visit. The repeat sitting measurements were made at 2 to 3 minute intervals and the mean of three sSBP measurements were used as the average sitting office blood pressure for that visit. (NCT01365481)
Timeframe: Baseline, End Point (Week 78 or Last observation carried forward (LOCF)

Interventionmillimeter(s) of mercury (mmHg) (Mean)
Valsartan + Antihypertensive Group-13.3
Valsartan Alone-15.5

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Percentage of Chronic Kidney Disease (CKD) Patients Who Had Estimated Glomerular Filtration Rate (eGFR) Decrease > 25 % From Baselinefrom Baseline to End Point

Percentage of Patients with CKD who had eGFR decrease > 25 % from Baseline (NCT01365481)
Timeframe: Baseline, End Point (Week 78 or Last observation carried forward (LOCF)

InterventionPercentage of patients (Number)
Valsartan + Antihypertensive Group30.4
Valsartan Alone27.5

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Percentage of Chronic Kidney Disease (CKD) Patients Who Had >=50% Reduction in Urine Albumin/Creatinine Ratio (UACR) From Baseline to End Point

Percentage of Patients with CKD who had Urine albumin creatinine reduction >/= 50% from baseline (NCT01365481)
Timeframe: Baseline, End Point (Week 78 or Last observation carried forward (LOCF)

InterventionPercentage of patients (Number)
Valsartan + Antihypertensive Group50.0
Valsartan Alone41.9

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Change From Baseline in Urine Potassium at 24 Hours Post-dose on Day 28

Urine potassium (K+) levels were measured over 24-hours on Day -1 and on Day 28. The total amount of K+ excreted in the urine for Day-1 (baseline) and Day 28 were calculated and the difference between the 2 values was recorded. (NCT01370655)
Timeframe: Baseline (Day -1) and Day 28

Interventionmmol/day (Least Squares Mean)
MK-7145 3 mg0.3
MK-7145 6 mg-6.5
HCTZ 25 mg-2.7
Placebo-7.6

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Change From Baseline in Time-weighted Average Over 24 Hours Post Dose (TWA [0-24]) in Systolic Blood Pressure (SBP)

Each participant had their blood pressure monitored by continuous 24-hour ambulatory blood pressure monitoring (ABPM) on Days -1 and 28 of each treatment period. The average systolic blood pressure over the 24-hour monitoring period was calculated for baseline (Day -1) and Day 28. The difference between baseline and Day 28 was calculated and recorded. (NCT01370655)
Timeframe: Baseline and Day 28

InterventionmmHg (Least Squares Mean)
MK-7145 3 mg-9.5
MK-7145 6 mg-10.2
HCTZ 25 mg-4.8
Placebo-2.8

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Change From Baseline in Time-weighted Average Over 24 Hours Post Dose (TWA [0-24]) in Diastolic Blood Pressure (DBP)

Each participant had their blood pressure monitored by continuous 24-hour ambulatory blood pressure monitoring (ABPM) on Days -1 and 28 of each treatment period. The average diastolic blood pressure over the 24-hour monitoring period was calculated for baseline (Day -1) and Day 28. The difference between baseline and Day 28 was calculated and recorded. (NCT01370655)
Timeframe: Baseline and Day 28

InterventionmmHg (Least Squares Mean)
MK-7145 3 mg-4.5
MK-7145 6 mg-4.3
HCTZ 25 mg-1.5
Placebo-1.1

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Change From Baseline in Urine Sodium at 24 Hours Post-dose on Day 1

Urine sodium (Na) levels were measured over 24-hours on Day -1 (baseline) and on Day 1. The total amount of Na excreted in the urine for Day-1 (baseline) and Day1 were calculated and the difference between the 2 values was recorded. (NCT01370655)
Timeframe: Baseline (Day-1) and Day 1

Interventionmmol/day (Least Squares Mean)
MK-7145 3 mg0.4
MK-7145 6 mg46.0
HCTZ 25 mg64.1
Placebo-30.5

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Percentage of Participants Who Had Study Discontinued During the Study Due to an Adverse Event (AE)

An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE. The percentage of participants who had the administration of the study drug discontinued during the study was summarized by study drug taken at the time of the AE. Participants may or may not have completed the study. (NCT01370655)
Timeframe: up to 4 weeks of each treatment period

InterventionPercentage of Participants (Number)
MK-7145 3 mg0
MK-7145 6 mg10.7
HCTZ 25 mg7.7
Placebo5.3

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Percentage of Participants Who Experienced at Least 1 Adverse Event (AE)

An AE was defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally associated with the use of the product, whether or not considered related to the use of the product. Any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a preexisting condition which was temporally associated with the use of the product, was also an AE. The percentage of participants who experienced an AE during the study was summarized by study drug taken at the time of the AE. (NCT01370655)
Timeframe: Up to 14 days post last dose of each treatment period (total of 6 weeks for each treatment period)

InterventionPercentage of Participants (Number)
MK-7145 3 mg84.2
MK-7145 6 mg78.6
HCTZ 25 mg73.1
Placebo47.4

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Renal Oxygenation Changes After Chronic Treatment With Aliskiren or Hydrochlorothiazide

Changes in R2* at between week 0 and week 8 as measured by BOLD MRI in the cortex and medulla of the kidney (NCT01519635)
Timeframe: week 0 vs week 8

,
Intervention1/sec (Mean)
Cortex week 0Cortex week 8
Aliskiren20.519.5
Hydrochlorothiazide19.520.5

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Blood Pressure Control, as Defined as Office BP Measurement of <140 mmHg Systolic and <90 mmHg Diastolic

At each study visit (approximately every 30 days), participants' BP will be checked. If BP is controlled (<140mmHG systolic and <90mmHG diastolic), then current medication will continue. If BP is uncontrolled, medication will be revised every 30 days (up to 120) until BP control is achieved. (NCT01658657)
Timeframe: 4 months

Interventionparticipants (Number)
PRA-guided Therapy3
Fixed-dose Combination Treatment-guided Therapy1

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Change From Baseline in Mean 24-hour Ambulatory Pulse Pressure (maPP)

Mean 24 hour ambulatory pulse pressure was calculated as the difference between the mean 24 hour systolic and diastolic ambulatory blood pressure in corresponding visits i.e. baseline, week 12 and week 52. (NCT01692301)
Timeframe: Baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to Week 12 (n=164, 162 )Baseline to week 52 (n=174, 176)
LCZ696 (Sacubitril/Valsartan)-5.77-5.26
Olmesartan-3.69-5.91

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Change From Baseline in Mean 24-hour Systolic Blood Pressure (maSBP)

An Ambulatory Blood Pressure Monitor (ABPM) measured a participant's blood pressure over a 24 hour period using an automated validated monitoring device at baseline, week 12 and at week 52 starting one day before each visit. The 24 hour maSBP was calculated by taking the mean of all ambulatory systolic blood pressure readings for the 24 hour period. (NCT01692301)
Timeframe: Baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to week 12 (n= 164, 162)Baseline to week 52 (n= 174, 176)
LCZ696 (Sacubitril/Valsartan)-13.25-14.15
Olmesartan-9.14-14.32

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Change From Baseline in Mean Arterial Pressure (MAP)

Mean arterial pressure (MAP) was calculated from mean sitting systolic BP (msSBP) and mean sitting diastolic BP (msDBP) as (2 * msDBP + msSBP)/3. (NCT01692301)
Timeframe: baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to week 12 (n=226, 222)Baseline to week 52 (n=226, 223)
LCZ696 (Sacubitril/Valsartan)-12.19-13.92
Olmesartan-8.57-12.38

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Change From Baseline in Mean Central Pulse (CPP) Pressure

(NCT01692301)
Timeframe: Baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to Week 12 (n = 207, 206)Baseline to Week 52 (n = 209, 208)
LCZ696 (Sacubitril/Valsartan)-6.41-7.16
Olmesartan-3.96-6.65

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Change From Baseline in Mean Pulse Wave Velocity (PWV)

"Pulse wave velocity recordings were performed on patient while in a supine, face-up position.~Tonometry was performed on the carotid simultaneously with the cuff inflation over the femoral artery. Two pulse wave velocity measures, meeting all quality control criteria were captured at baseline, week 12 and week 52." (NCT01692301)
Timeframe: baseline, 12 weeks, and 52 weeks

,
Interventionmeter/second (Least Squares Mean)
Baseline to week 12 (n= 192, 196)Baseline to week 52 ( n= 199, 199)
LCZ696 (Sacubitril/Valsartan)-0.68-0.83
Olmesartan-0.570.77

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Change From Baseline in Mean Sitting Diastolic Blood Pressure (msDBP)

At the first study visit, the patient had his/her blood pressure (BP) measured in both arms; the arm in which the highest sitting SBP was found was used for all subsequent readings throughout the study. At each study visit, after the patient had been sitting for 5 minutes, DBP were measured 3 times using a standard mercury sphygmomanometer and appropriate size cuff. The repeat sitting measurements were made at 1- to 2-minute intervals and the mean of those 3 measurements was used as the average sitting office BP for that visit. (NCT01692301)
Timeframe: baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to week 12 (n=226, 222)Baseline to week 52 (n=226,223)
LCZ696 (Sacubitril/Valsartan)-7.86-8.92
Olmesartan-5.58-7.85

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Change From Baseline in Mean 24-hour Diastolic Blood Pressure (maDBP)

An Ambulatory Blood Pressure Monitor (ABPM) measured a participant's blood pressure over a 24 hour period using an automated validated monitoring device at baseline, week 12 and at week 52 starting one day before each visit. The 24 hour maDBP was calculated by taking the mean of all ambulatory systolic blood pressure readings for the 24 hour period. (NCT01692301)
Timeframe: Baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to week 12 (n= 164, 162)Baseline to week 52 (n= 174, 176)
LCZ696 (Sacubitril/Valsartan)-7.44-8.85
Olmesartan-5.48-8.44

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Change From Baseline in Mean Central Aortic Systolic Pressure (CASP) at 12 Weeks

"Central aortic blood pressure was derived from peripheral pressure waveforms recorded noninvasively from the brachial artery using a cuff-based device. This technique uses the brachial pressure and a signal processing algorithm to transform brachial signals into central blood pressure (BP) waveforms. When the aortic pressure waveform was derived, key pulse wave analysis (PWA) parameters, such as CASP was calculated by the system software.~At the first study visit, the arm with the highest systolic blood pressure (SBP) was used for all subsequent PWA. Brachial PWA measurements were performed on the same arm that the office blood pressures were taken. Two pulse waveform measurements, meeting all quality control criteria were captured at baseline and at week 12 visits." (NCT01692301)
Timeframe: baseline, 12 weeks

InterventionmmHg (Least Squares Mean)
LCZ696 (Sacubitril/Valsartan)-12.57
Olmesartan-8.90

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Change From Baseline in Mean Central Aortic Systolic Pressure (CASP) at 52 Weeks

"Central aortic blood pressure was derived from peripheral pressure waveforms recorded noninvasively from the brachial artery using a cuff-based device. This technique uses the brachial pressure and a signal processing algorithm to transform brachial signals into central blood pressure (BP) waveforms. When the aortic pressure waveform was derived, key pulse wave analysis (PWA) parameters, such as CASP was calculated by the system software.~At the first study visit, the arm with the highest systolic blood pressure (SBP) was used for all subsequent PWA. Brachial PWA measurements were performed on the same arm that the office blood pressures were taken. Two pulse waveform measurements, meeting all quality control criteria were captured at baseline and at week 12 visits." (NCT01692301)
Timeframe: baseline, 52 weeks

InterventionmmHg (Least Squares Mean)
LCZ696 (Sacubitril/Valsartan)-16.18
Olmesartan-14.70

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Change From Baseline in Mean Sitting Pulse Pressure (msPP)

Mean sitting pulse pressure for each patient and visit was calculated as the difference between the calculated values of mean sitting systolic blood pressure and mean sitting diastolic blood pressure. (NCT01692301)
Timeframe: baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to week 12 (n=226,222)Baseline to week 52 (n= 226, 223)
LCZ696 (Sacubitril/Valsartan)-13.13-15.02
Olmesartan-8.86-13.58

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Change From Baseline in Mean Sitting Systolic Blood Pressure (msSBP)

At the first study visit, the patient had his/her blood pressure (BP) measured in both arms; the arm in which the highest sitting SBP was found was used for all subsequent readings throughout the study. At each study visit, after the patient had been sitting for 5 minutes, SBP were measured 3 times using a standard mercury sphygmomanometer and appropriate size cuff. The repeat sitting measurements were made at 1- to 2-minute intervals and the mean of those 3 measurements was used as the average sitting office BP for that visit. (NCT01692301)
Timeframe: baseline, 12 weeks, and 52 weeks

,
InterventionmmHg (Least Squares Mean)
Baseline to week 12 (n=226, 222)Baseline to week 52 (n=226,223)
LCZ696 (Sacubitril/Valsartan)-20.84-23.91
Olmesartan-14.57-21.45

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Change From Baseline in Mean Seated DBP at Trough After 8 Weeks of the Double-blind Period.

Change from baseline in mean seated diastolic blood pressure (DBP) at trough (24-hour post dosing) after 8 weeks of the double-blind period. The results are presented as 'change' rather than 'reduction' i.e., reductions are expressed with negative values'. The 'adjusted mean' is shown as 'mean'. (NCT01911780)
Timeframe: baseline and 8 weeks

InterventionmmHg (Mean)
Telmisartan + HCTZ + Amlodipine-8.8
Telmisartan + HCTZ + Placebo-1.3

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Change From Baseline in Mean Seated SBP at Trough After 8 Weeks of the Double-blind Period.

Change from baseline in mean seated systolic blood pressure (SBP) at trough after 8 weeks of the double-blind period. The results are presented as 'change' rather than 'reduction' i.e., reductions are expressed with negative values'. The 'adjusted mean' is shown as 'mean'. (NCT01911780)
Timeframe: baseline and 8 weeks

InterventionmmHg (Mean)
Telmisartan + HCTZ + Amlodipine-10.6
Telmisartan + HCTZ + Placebo-2.1

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The Percentage of Patients With DBP<90 mmHg and SBP<140 mmHg Blood Pressure at Trough After 8 Weeks of Double-blind Period.

The percentage of patients with DBP<90 mmHg and SBP<140 mmHg as seated blood pressure at trough after 8 weeks of the double-blind period. The results are presented as 'change' rather than 'reduction' i.e., reductions are expressed with negative values'. The 'adjusted mean' is shown as 'mean'. (NCT01911780)
Timeframe: Double-blind and 8 weeks

InterventionParticipants (Number)
Telmisartan + HCTZ + Amlodipine44.8
Telmisartan + HCTZ + Placebo21.9

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Change From Baseline in Mean DBP Pressure at Trough After 52 Weeks of the Extension Period.

"Change from baseline in mean seated diastolic blood pressure at trough after 52 weeks of the extension period. Note, week 52 of the extension period corresponds to 60 weeks after the reference baseline.~The results are presented as 'change' rather than 'reduction' i.e., reductions are expressed with negative values'. The 'adjusted mean' is shown as 'mean'." (NCT01911780)
Timeframe: Reference baseline (week 0) and week 60 (end of extension period)

,
InterventionmmHg (Mean)
MeanAdjusted mean
Telmisartan + HCTZ + Amlodipine + Ext-11.4-10.9
Telmisartan + HCTZ + Placebo + Ext-10.0-10.5

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Change From Baseline in Mean Seated SBP at Trough After 52 Weeks of the Extension Period.

"Change from baseline in mean seated systolic blood pressure at trough after 52 weeks of the extension period. Note, week 52 of the extension period corresponds to 60 weeks after the reference baseline.~The results are presented as 'change' rather than 'reduction' i.e., reductions are expressed with negative values'. The 'adjusted mean' is shown as 'mean'." (NCT01911780)
Timeframe: Reference baseline (week 0) and week 60 (end of extension period)

,
InterventionmmHg (Mean)
MeanAdjusted mean
Telmisartan + HCTZ + Amlodipine + Ext-14.8-13.6
Telmisartan + HCTZ + Placebo + Ext-14.3-15.9

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The Number of Patients With DBP<90 mmHg and SBP<140 mmHg Blood Pressure at Trough After 52 Weeks of Extension Period.

"The number of patients with DBP<90 mmHg and SBP<140 mmHg as seated blood pressure at trough after 52 weeks of the extension period. Note, week 52 of the extension period corresponds to 60 weeks after the reference baseline.~The results are presented as 'change' rather than 'reduction' i.e., reductions are expressed with negative values'. The 'adjusted mean' is shown as 'mean'." (NCT01911780)
Timeframe: Reference baseline (week 0) and week 60 (end of extension period)

,
InterventionParticipants (Number)
YesNo
Telmisartan + HCTZ + Amlodipine4124
Telmisartan + HCTZ + Placebo3328

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Change From Baseline in Mean Seated DBP at Trough After 8 Weeks of the Double-blind Period.

Change from baseline in mean seated diastolic blood pressure (DBP) at trough after 8 weeks of the double-blind period. After patients had rested in a seated position for approximately 5 minutes, blood pressure was measured 3 times at approximately 2-minute intervals. The mean of the 3 measurements are used as endpoints. (NCT01975246)
Timeframe: baseline and week 8

InterventionmmHg (Mean)
Telmisartan and Amlodipine+HCTZ-8.4
Telmisartan+Amlodipine-4.5

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Change From Baseline in Mean Seated SBP at Trough After 8 Weeks of the Double-blind Period.

Change from baseline in mean seated systolic blood pressure (SBP) at trough after 8 weeks of the double-blind period. After patients had rested in a seated position for approximately 5 minutes, blood pressure was measured 3 times at approximately 2-minute intervals. The mean of the 3 measurements are used as endpoints. (NCT01975246)
Timeframe: baseline and week 8

InterventionmmHg (Mean)
Telmisartan and Amlodipine+HCTZ-12.3
Telmisartan+Amlodipine-6.9

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The Proportion of Patients With DBP<90 mmHg and SBP<140 mmHg as Seated Blood Pressure at Trough After 8 Weeks of the Double-blind Period

Patients with trough seated DBP =>90 mmHg or trough seated SBP >=140 mmHg at baseline were analysed. (NCT01975246)
Timeframe: baseline and week 8

Interventionpercentage of participants (Number)
Telmisartan and Amlodipine+HCTZ51.7
Telmisartan+Amlodipine36.9

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Aortic Stiffness

Carotid-femoral pulse wave velocity (PWV) (NCT01983462)
Timeframe: 4 weeks

,,
Interventionmeters/sec (Mean)
Baseline4 weeks
Clonidine7.97.3
Hydrochlorothiazide7.07.0
Placebo8.18.0

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24 Hour Average Systolic Blood Pressure

24 hour ambulatory systolic blood pressure (NCT01983462)
Timeframe: 4 weeks

,,
InterventionmmHg (Mean)
Baseline4 weeks
Clonidine133126
Hydrochlorothiazide135131
Placebo133134

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Changes From Baseline in Systolic Blood Pressure (SBP) at Each Time Point

Reported data are changes in SBP from baseline at Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and final assessment. (NCT02016183)
Timeframe: Baseline, and Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and Final assessment (up to 12 months)

InterventionmmHg (Mean)
Change in SBP at Month 1Change in SBP at Month 2Change in SBP at Month 3Change in SBP at Month 4Change in SBP at Month 5Change in SBP at Month 6Change in SBP at Month 7Change in SBP at Month 8Change in SBP at Month 9Change in SBP at Month 10Change in SBP at Month 11Change in SBP at Month 12Change in SBP at Final
Candesartan Cilexetil/Hydrochlorothiazide-13.3-14.8-15.4-15.7-15.6-16.1-15.8-15.8-16.4-16.6-17.0-18.1-17.5

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Changes From Baseline in Diastolic Blood Pressure (DBP) at Each Time Point

Reported data are changes in DBP from baseline at Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and final assessment. (NCT02016183)
Timeframe: Baseline, and Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and Final assessment (up to 12 months)

InterventionmmHg (Mean)
Change in DBP at Month 1Change in DBP at Month 2Change in DBP at Month 3Change in DBP at Month 4Change in DBP at Month 5Change in DBP at Month 6Change in DBP at Month 7Change in DBP at Month 8Change in DBP at Month 9Change in DBP at Month 10Change in DBP at Month 11Change in DBP at Month 12Change in DBP at Final
Candesartan Cilexetil/Hydrochlorothiazide-6.5-7.3-7.6-7.8-7.8-8.0-8.1-8.2-8.5-8.7-8.5-9.1-8.5

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Number of Participants Who Experience at Least One Adverse Drug Reactions (ADRs)

ADRs are defined as adverse events (AEs) which are in the investigator's opinion of causal relationship to the study treatment. AEs are defined as any unfavorable and unintended signs, symptoms or diseases temporally associated with the use of a medicinal product reported from the first dose of study drug to the last dose of study drug. (NCT02016183)
Timeframe: Up to 12 months

InterventionParticipants (Count of Participants)
Candesartan Cilexetil/Hydrochlorothiazide283

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Changes From Baseline in Pulse Rate at Each Time Point

Reported data are changes in Pulse Rate from baseline at Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and final assessment. (NCT02016183)
Timeframe: Baseline, and Month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and Final assessment (up to 12 months)

InterventionBeats per minutes (Mean)
Change in Pulse Rate at Month 1Change in Pulse Rate at Month 2Change in Pulse Rate at Month 3Change in Pulse Rate at Month 4Change in Pulse Rate at Month 5Change in Pulse Rate at Month 6Change in Pulse Rate at Month 7Change in Pulse Rate at Month 8Change in Pulse Rate at Month 9Change in Pulse Rate at Month 10Change in Pulse Rate at Month 11Change in Pulse Rate at Month 12Change in Pulse Rate at Final assessment
Candesartan Cilexetil/Hydrochlorothiazide-1.3-1.1-1.3-1.5-1.3-1.5-1.1-1.5-1.6-1.7-1.5-1.8-1.6

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Change in the Level of Urinary Free Light Chains

In relation to kidney function and washout/reintroduction of ACE/ARB medication the level of urinary free light chains will be assessed. (NCT02046395)
Timeframe: Visit 1 (Baseline), Visit 3 (Day 60)

Interventionmg/g (Mean)
Alternate Antihypertensive Arm1.14

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Change in Urine Microalbumin Creatinine Ratio

Kidney function will be assessed throughout the study to assess changes in function prior to the washout of ACE/ARB medication and reintroduction of the ACE/ARB medication. (NCT02046395)
Timeframe: Visit 1 (Baseline), Visit 3 (Day 60)

Interventionmg/g (Mean)
Alternate Antihypertensive Arm15

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Maximum Measured Concentration (Cmax) at Steady State for HCTZ

Maximum measured concentration (Cmax) of HCTZ in plasma at steady state over the dosing interval tau (NCT02183675)
Timeframe: 15 minutes (min) before drug administration and 15min, 30min, 45min, 1 hour (h), 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 12h, 24h, 32h and 48h after 10 days drug administration

Interventionng/mL (Geometric Mean)
T80-A5-H12.5107
T80-H12.5102

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Maximum Measured Concentration (Cmax) at Steady State for Amlodipine

Maximum measured concentration (Cmax) of amlodipine in plasma at steady state over the dosing interval tau (NCT02183675)
Timeframe: 15 minutes (min) before drug administration and 15min, 30min, 45min, 1 hour (h), 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 12h, 24h, 32h, 48h, 72h, 96h, 120h and 144h after 10 days drug administration

Interventionng/mL (Geometric Mean)
T80-A5-H12.511.8
T80-A511.3

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Area Under the Plasma Concentration Curve at Steady State for Telmisartan

Area under the plasma concentration curve (AUC) of telmisartan in plasma at steady state over the dosing interval tau (NCT02183675)
Timeframe: 15 minutes (min) before drug administration and 15min, 30min, 45min, 1 hour (h), 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 12h, 24h, 32h, 48h and 72h after 10 days drug administration

Interventionng*h/mL (Geometric Mean)
T80-A5-H12.52510
T80-A52570
T80-H12.52580

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Area Under the Plasma Concentration Curve at Steady State for HCTZ

Area under the plasma concentration curve (AUC) of HCTZ in plasma at steady state over the dosing interval tau (NCT02183675)
Timeframe: 15 minutes (min) before drug administration and 15min, 30min, 45min, 1 hour (h), 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 12h, 24h, 32h and 48h after 10 days drug administration

Interventionng*h/mL (Geometric Mean)
T80-A5-H12.5584
T80-H12.5565

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Area Under the Plasma Concentration Curve at Steady State for Amlodipine

Area under the plasma concentration curve (AUC) of amlodipine in plasma at steady state over the dosing interval tau (NCT02183675)
Timeframe: 15 minutes (min) before drug administration and 15min, 30min, 45min, 1 hour (h), 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 12h, 24h, 32h, 48h, 72h, 96h, 120h and 144h after 10 days drug administration

Interventionng*h/mL (Geometric Mean)
T80-A5-H12.5230
T80-A5223

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Amount of HCTZ Excreted in Urine at Steady State From 0 to 24 Hours

Amount of HCTZ excreted in urine over the time interval from 0 to 24 hours at steady state (NCT02183675)
Timeframe: 0-6 hours (h), 6-12h and 12-24h after drug administration on day 10

Interventionmg (Geometric Mean)
T80-A5-H12.510.4
T80-H12.59.9

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Maximum Measured Concentration (Cmax) at Steady State for Telmisartan

Maximum measured concentration (Cmax) of telmisartan in plasma at steady state over the dosing interval tau (NCT02183675)
Timeframe: 15 minutes (min) before drug administration and 15min, 30min, 45min, 1 hour (h), 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 12h, 24h, 32h, 48h and 72h after 10 days drug administration

Interventionng/mL (Geometric Mean)
T80-A5-H12.5970
T80-A5857
T80-H12.5895

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Medication Adherence-Percentage of Pills Taken

polypill arm-evaluation via pill counts. (NCT02278471)
Timeframe: 12 months

Interventionpercentage of pills taken (Median)
Polypill86

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Systolic Blood Pressure

polypill versus usual care (NCT02278471)
Timeframe: 2 months

Interventionmm Hg (Mean)
Usual Care133
Polypill128

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Systolic Blood Pressure

polypill versus usual care (NCT02278471)
Timeframe: 12 months

Interventionmm Hg (Mean)
Usual Care138
Polypill131

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Medication Adherence

polypill-percentage of pills taken, evaluated via pill counts (NCT02278471)
Timeframe: 2 months

Interventionpercentage of pills taken (Median)
Polypill98

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LDL Cholesterol

polypill versus usual care (NCT02278471)
Timeframe: 2 months

Interventionmg/dL (Mean)
Usual Care108
Polypill90

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LDL Cholesterol

Polypill versus usual care (NCT02278471)
Timeframe: 12 months

Interventionmg/dL (Mean)
Usual Care109
Polypill98

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The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target at 12 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 12 weeks. Blood pressure was measured at week 14 of the trial. (NCT02336607)
Timeframe: 12 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)NANA
Felodipine Tablet (Plendil)+Hydrochlorothiazide-18.2-12.2
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-18.4-13.0
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-20.3-13.6

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The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target After 8 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 8 weeks. Blood pressure was measured at week 10 of the trial. (NCT02336607)
Timeframe: 8 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)NANA
Felodipine Tablet (Plendil)+Hydrochlorothiazide-18.5-11.5
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-19.4-13.4
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-19.7-13.1

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The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among All Randomized Subjects After 8 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 8 weeks. Blood pressure was measured at week 10 of the trial. (NCT02336607)
Timeframe: 8 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)NANA
Felodipine Tablet (Plendil)+Hydrochlorothiazide-16.4-10.7
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-17.8-11.3
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-18.0-12.1

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The Magnitude of Systolic and Diastolic Blood Pressure Change From Baseline Among All Randomized Subjects After 4 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 4 weeks. Blood pressure was measured at week 6 of the trial. (NCT02336607)
Timeframe: 4 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)NANA
Felodipine Tablet (Plendil)+Hydrochlorothiazide-9.8-6.0
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-10.3-7.3
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-13.4-9.9

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The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among All Randomized Subjects After 12 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 12 weeks. Blood pressure was measured at week 14 of the trial. (NCT02336607)
Timeframe: 12 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)NANA
Felodipine Tablet (Plendil)+Hydrochlorothiazide-16.8-10.6
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-16.6-10.7
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-18.0-12.8

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The Change of Pulse Wave Velocity From Baseline at 2, 14 Weeks of Felodipine Sustained Release Alone.

The duration of the combination therapy was 12 weeks. The change of pulse wave velocity was measured at week 14 of the trial. (NCT02336607)
Timeframe: 12 weeks

,,,
Interventionm/s (Mean)
week 2week 14
Felodipine Tablet (Plendil)-0.58-0.86
Felodipine Tablet (Plendil)+HydrochlorothiazideNANA
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)NANA
Felodipine Tablets (Plendil)+Lisinopril (Zestril)NANA

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The Percentage of Subjects Reaching Blood Pressure Target (Defined as < 140 / 90 mmHg) After 4 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 4 weeks. Blood pressure was measured at week 6 of the trial. (NCT02336607)
Timeframe: 4 weeks

InterventionPercentage (Number)
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)45.8
Felodipine Tablets (Plendil)+Lisinopril (Zestril)59.5
Felodipine Tablet (Plendil)+Hydrochlorothiazide46.2
Felodipine Tablet (Plendil)NA

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The Change of Pulse Wave Velocity at 12 Weeks Compare With Baseline Data of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 12 weeks. The change of pulse wave velocity was measured at week 14 of the trial. (NCT02336607)
Timeframe: 12 weeks

Interventionm/s (Mean)
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-0.12
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-0.44
Felodipine Tablet (Plendil)+Hydrochlorothiazide-0.06
Felodipine Tablet (Plendil)NA

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The Percentage of Subjects Reaching Blood Pressure Target (Defined as < 140 / 90 mmHg) After 8 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 8 weeks. Blood pressure was measured at week 10 of the trial. (NCT02336607)
Timeframe: 8 weeks

InterventionPercentage (Number)
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)78.6
Felodipine Tablets (Plendil)+Lisinopril (Zestril)79
Felodipine Tablet (Plendil)+Hydrochlorothiazide78.7
Felodipine Tablet (Plendil)NA

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The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target at 4 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

The duration of the combination therapy was 4 weeks. Blood pressure was measured at week 6 of the trial. (NCT02336607)
Timeframe: 4 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)NANA
Felodipine Tablet (Plendil)+Hydrochlorothiazide-16.4-8.2
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)-16.1-12.3
Felodipine Tablets (Plendil)+Lisinopril (Zestril)-17.1-10.9

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The Magnitude of Systolic and Diastolic Blood Pressure Changes From Baseline Among the Subjects Who Reached Target at 2 Weeks of Felodipine Sustained Release, Alone

The duration of the combination therapy was 2 weeks. Blood pressure was measured at week 2 of the trial. (NCT02336607)
Timeframe: 2 weeks

,,,
InterventionmmHg (Mean)
Change of systolic blood pressureChange of diastolic blood pressure
Felodipine Tablet (Plendil)-22.8-15.1
Felodipine Tablet (Plendil)+HydrochlorothiazideNANA
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)NANA
Felodipine Tablets (Plendil)+Lisinopril (Zestril)NANA

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The Percentage of Subjects Reaching Blood Pressure Target (Defined as < 140 / 90 mmHg) After 14 Weeks of Felodipine Sustained Release in Combination With Metoprolol, Lisinopril or Hydrochlorothiazide.

(NCT02336607)
Timeframe: 14 weeks

InterventionPercentage (Number)
Felodipine Tablet (Plendil)+Metoprolol Tablet (Betaloc ZOK)74.1
Felodipine Tablets (Plendil)+Lisinopril (Zestril)80.5
Felodipine Tablet (Plendil)+Hydrochlorothiazide80.2
Felodipine Tablet (Plendil)NA

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The Number of Patients for Whom Each Drug is Selected as the Preferred Therapy

For each n-of-1 trial, the preferred drug is defined as that which produces normal ambulatory blood pressure (by pediatric Ambulatory blood pressure monitoring (ABPM) standards), with the greatest magnitude of wake mean systolic BP reduction, and without unacceptable side effects. (NCT02412761)
Timeframe: The outcome of BP control and side effect tolerability will be assessed 2 weeks after starting each drug. Participants will be followed for an average of 10-12 weeks.

InterventionParticipants (Count of Participants)
Lisinopril16
Amlodipine8
Hydrochlorothiazide4

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Brachial Artery Flow Mediated Dilation

Brachial Artery Flow Mediated Dilation is upper arm brachial artery dilation during the 3 minutes forearm reactive hyperemia following the release of the 5-minute forearm cuff occlusion. (NCT02699125)
Timeframe: At the end of 2 weeks of placebo therapy, at the end of 6 weeks of guanfacine therapy and at the end of 6 weeks of hydrochlorothiazide therapy.

Interventionpercentage of the preoclussion diameter (Mean)
Placebo4.5
Guanfacine8.4
Hydrochlorothiazide4.9

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24-h, Wake and Sleep Period Systolic and Diastolic Blood Pressure

"The primary outcome measure is ambulatory systolic and diastolic blood pressure recorded once every 15 minutes during the day and once every 30 minutes during the sleep. The Outcome Measure Data Table present primary outcome as 24-h, Wake and Sleep Period Systolic and Diastolic Blood Pressure after each of the following three interventions: Placebo, Guanfacine and Hydrochlorothiazide." (NCT02699125)
Timeframe: At the end of 2 weeks of placebo therapy, at the end of 6 weeks of guanfacine therapy and at the end of 6 weeks of hydrochlorothiazide therapy.

,,
InterventionmmHg (Mean)
24-h systolic blood pressure24-h diastolic blood pressureWake systolic blood pressureWake diastolic blood pressureSleep systolic blood pressureSleep diastolic blood pressure
Guanfacine133811378412473
Hydrochlorothyazide136831398613076
Placebo143871479113680

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24-h, Wake and Sleep Period Systolic and Diastolic Blood Pressure

"24-h Systolic Blood Pressure is the average of all 24-h Ambulatory Systolic Blood Pressure recordings. The Wake Period Systolic Blood Pressure is the average of all Systolic Blood Pressures recorded every 15 minutes during the wake period. The Sleep Period Systolic Blood pressure is the average of all Systolic Blood Pressures recorded every 30 minutes during the sleep period.~24-h Diastolic Blood Pressure is the average of all 24-h Ambulatory Diastolic Blood Pressure recordings. The Wake Period Diastolic Blood Pressure is the average of all Diastolic Blood Pressures recorded every 15 minutes during the wake period. The Sleep Period Diastolic Blood pressure is the average of all Diastolic Blood Pressures recorded every 30 minutes during the sleep period." (NCT02710071)
Timeframe: At the end of 2 weeks of placebo therapy, at the end of 6 weeks of Nebivolol therapy and at the end of 6 weeks of hydrochlorothiazide therapy.

,,
InterventionmmHg (Mean)
24-h systolic blood pressure24-h diastolic blood pressureWake systolic blood pressureWake diastolic blood pressureSleep systolic blood pressureSleep diastolic blood pressure
Hydrochlorothiazide133801388512775
Nebivolol130771358112371
Placebo137821418612976

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Blood Urea Nitrogen (BUN) Levels at Indicated Time Points

Serum BUN levels were assessed as a clinical chemistry laboratory parameter at Day -1 and Day 3 in each treatment period. Only those participants available at the specified time points were analyzed (represented by n=X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionMilligrams per deciliter (mg/dL) (Mean)
P1; Day-1; 24 hour pre-dose; n=21, 21P1; Day 3; 48 hour post-dose; n=21, 20P2; Day -1; 24 hour pre-dose; n=19, 19P2; Day 3; 48 hour post-dose; n=19, 19
Treatment A12.51914.97012.18516.372
Treatment B12.70215.59312.16415.208

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Body Temperature Values at Indicated Time Points

Vital sign measurements including body temperature were taken in a supine position after at least 5 minutes of rest at Day -1, Day 1, Day 2 and Day 3 in each treatment period. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionDegree Celsius (Mean)
P1; Day-1; 12 hour pre-dose; n= 21, 21P1; Day1; 1 hour post-dose; n= 21, 21P1; Day1; 1.5 hour post-dose; n= 21, 21P1; Day1; 2 hour post-dose; n= 21, 21P1; Day1; 4 hour post-dose; n= 21, 21P1; Day1; 6 hour post-dose; n= 21, 21P1; Day1; 8 hour post-dose; n= 21, 21P1; Day2; 24 hour post-dose; n= 21, 21P1; Day3; 48 hour post-dose; n= 21, 20P2; Day-1; 12 hour pre-dose; n= 19, 19P2; Day1; 1 hour post-dose; n= 19, 19P2; Day1; 1.5 hour post-dose; n= 19, 19P2; Day1; 2 hour post-dose; n= 19, 19P2; Day1; 4 hour post-dose; n= 19, 19P2; Day1; 6 hour post-dose; n= 19, 19P2; Day1; 8 hour post-dose; n= 19, 19P2; Day2; 24 hour post-dose; n= 19, 19P2; Day3; 48 hour post-dose; n= 18, 19
Treatment A36.4236.4436.0636.4236.4536.5936.6436.2836.2636.4136.2836.0636.4136.5336.5936.6436.1536.08
Treatment B36.4336.4036.0536.3836.4636.6136.7536.3036.2836.3436.2436.1936.3836.4436.5736.6536.1736.28

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Calcium, Chloride, Glucose, Magnesium, Potassium and Sodium Levels at Indicated Time Points

Serum calcium, chloride, glucose, magnesium, potassium and sodium levels were assessed as a clinical chemistry laboratory parameter at Day -1 and Day 3 in each treatment period. Only those participants available at the specified time points were analyzed (represented by n=X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionMillimoles per liter (Mmol/L) (Mean)
Calcium; P1; Day-1; 24 hour pre-dose; n= 21, 21Calcium; P1; Day 3; 48 hour post-dose; n= 21, 20Calcium; P2; Day-1; 24 hour pre-dose; n= 19, 19Calcium; P2; Day 3; 48 hour post-dose; n= 19, 19Chloride; P1; Day-1; 24 hour pre-dose; n= 21, 21Chloride; P1; Day 3; 48 hour post-dose; n= 21, 20Chloride; P2; Day-1; 24 hour pre-dose; n= 19, 19Chloride; P2; Day 3; 48 hour post-dose; n= 19, 19Glucose; P1; Day-1; 24 hour pre-dose; n= 21, 20Glucose; P1; Day 3; 48 hour post-dose; n= 21, 20Glucose; P2; Day-1; 24 hour pre-dose; n= 19, 19Glucose; P2; Day 3; 48 hour post-dose; n= 19, 19Magnesium; P1; Day-1; 24 hour pre-dose; n= 21, 21Magnesium; P1; Day 3; 48 hour post-dose; n= 21, 20Magnesium; P2; Day-1; 24 hour pre-dose; n= 19, 19Magnesium; P2; Day 3; 48 hour post-dose; n= 19, 19Potassium; P1; Day-1; 24 hour pre-dose; n= 21, 21Potassium; P1; Day 3; 48 hour post-dose; n= 21, 20Potassium; P2; Day-1; 24 hour pre-dose; n= 19, 19Potassium; P2; Day 3; 48 hour post-dose; n= 19, 19Sodium; P1; Day-1; 24 hour pre-dose; n= 21, 21Sodium; P1; Day 3; 48 hour post-dose; n= 21, 20Sodium; P2; Day-1; 24 hour pre-dose; n= 19, 19Sodium; P2; Day 3; 48 hour post-dose; n= 19, 19
Treatment A2.4002.3962.3742.415104.80103.27104.36102.624.7465.0064.7544.6520.7820.7810.8260.8214.2874.3034.3004.364140.86138.90140.11139.11
Treatment B2.4182.3932.3352.379103.62102.63104.85103.494.6434.8274.7654.7320.8010.8040.8050.7834.2944.2224.2254.336140.67139.25139.68139.11

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Creatinine, Direct Bilirubin and Total Bilirubin Levels at Indicated Time Points

Serum creatinine, direct bilirubin and total bilirubin levels were assessed as a clinical chemistry laboratory parameter at Day -1 and Day 3 in each treatment period. Only those participants available at the specified time points were analyzed (represented by n=X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionMicromoles per liter (µmol/L) (Mean)
Creatinine; P1; Day-1; 24 hour pre-dose; n= 21, 21Creatinine; P1; Day3; 48 hour post-dose; n= 21, 20Creatinine; P2; Day-1; 24 hour pre-dose; n= 19, 19Creatinine; P2; Day3; 48 hour post-dose; n= 19, 19Direct bilirubin;P1;Day-1;24 hour pre-dose;n=21,21Direct bilirubin;P1;Day3;48 hour post-dose;n=21,20Direct bilirubin;P2;Day-1;24 hour pre-dose;n=19,19Direct bilirubin;P2;Day3;48 hour post-dose;n=19,19Total bilirubin;P1;Day-1;24 hour pre-dose;n=21,21Total bilirubin;P1;Day3;48 hour post-dose;n=21,20Total bilirubin;P2;Day-1;24 hour pre-dose;n=19,19Total bilirubin;P2;Day3;48 hour post-dose;n=19,19
Treatment A85.287.082.185.64.253.203.943.7712.109.4010.6110.83
Treatment B85.087.382.588.74.523.723.643.1413.4810.8010.088.67

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Number of Participants With Adverse Events (AEs) and Serious AEs (SAEs) During Treatment Period

An AE is any untoward medical occurrence in a clinical investigation participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. SAE is defined as any untoward medical occurrence that, at any dose results in death, is life threatening requires hospitalization or prolongation of existing hospitalization, results in disability, is a congenital anomaly/ birth effect, other situations and is associated with liver injury or impaired liver function. Only those participants with data available at the specified time points were analyzed (NCT03031496)
Timeframe: Up to 25 days

,
InterventionParticipants (Number)
AEsSAEs
Treatment A50
Treatment B80

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Percentage of AUC(0-inf) Obtained by Extrapolation (Percent AUCex) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma

Blood samples were collected at indicated time points under fasting conditions for PK analysis of hydrochlorothiazide and amiloride. Bioequivalence of test product and reference product was assessed based on the 90 percent CIs for estimates of the geometric mean ratios between percent AUCex of the test and reference products in relation to the conventional bioequivalence range. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Pre-dose, 0.33, 0.67, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10, 12,14, 16 hours post-dose on Day 1, 24 and 36 hours post dose on Day 2 and 48 hours post-dose on Day 3

,
InterventionPercent of area (Geometric Mean)
Hydrochlorothiazide; n= 37, 38Amiloride; n= 22, 22
Treatment A5.249.68
Treatment B4.6310.7

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Pulse Rate Values at Indicated Time Points

Vital sign measurements including pulse rate were taken in a supine position after at least 5 minutes of rest at Day -1, Day 1, Day 2 and Day 3 in each treatment period. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionBeats per minute (bpm) (Mean)
P1; Day-1; 12 hour pre-dose; n= 21, 21P1; Day1; 1 hour post-dose; n= 21, 21P1; Day1; 1.5 hour post-dose; n= 21, 21P1; Day1; 2 hour post-dose; n= 21, 21P1; Day1; 4 hour post-dose; n= 21, 21P1; Day1; 6 hour post-dose; n= 21, 21P1; Day1; 8 hour post-dose; n= 21, 21P1; Day2; 24 hour post-dose; n= 21, 21P1; Day3; 48 hour post-dose; n= 21, 20P2; Day-1; 12 hour pre-dose; n= 19, 19P2; Day1; 1 hour post-dose; n= 19, 19P2; Day1; 1.5 hour post-dose; n= 19, 19P2; Day1; 2 hour post-dose; n= 19, 19P2; Day1; 4 hour post-dose; n= 19, 19P2; Day1; 6 hour post-dose; n= 19, 19P2; Day1; 8 hour post-dose; n= 19, 19P2; Day2; 24 hour post-dose; n= 19, 19P2; Day3; 48 hour post-dose; n= 18, 19
Treatment A66.961.862.561.764.171.566.069.071.465.262.561.560.762.472.968.269.070.3
Treatment B64.762.060.960.762.570.867.868.673.065.260.162.859.262.771.466.268.873.4

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Respiratory Rate Values at Indicated Time Points

Vital sign measurements including respiratory rate were taken in a supine position after at least 5 minutes of rest at Day -1, Day 1, Day 2 and Day 3 in each treatment period. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionBreaths per minute (Mean)
P1; Day-1; 12 hour pre-dose; n= 21, 21P1; Day1; 1 hour post-dose; n= 21, 21P1; Day1; 1.5 hour post-dose; n= 21, 21P1; Day1; 2 hour post-dose; n= 21, 21P1; Day1; 4 hour post-dose; n= 21, 21P1; Day1; 6 hour post-dose; n= 21, 21P1; Day1; 8 hour post-dose; n= 21, 21P1; Day2; 24 hour post-dose; n= 21, 21P1; Day3; 48 hour post-dose; n= 21, 20P2; Day-1; 12 hour pre-dose; n= 19, 19P2; Day1; 1 hour post-dose; n= 19, 19P2; Day1; 1.5 hour post-dose; n= 19, 19P2; Day1; 2 hour post-dose; n= 19, 19P2; Day1; 4 hour post-dose; n= 19, 19P2; Day1; 6 hour post-dose; n= 19, 19P2; Day1; 8 hour post-dose; n= 19, 19P2; Day2; 24 hour post-dose; n= 19, 19P2; Day3; 48 hour post-dose; n= 18, 19
Treatment A16.516.316.717.016.917.216.918.217.117.917.715.818.017.917.218.717.518.4
Treatment B17.017.017.917.517.018.418.218.017.717.217.916.317.317.418.318.217.617.2

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Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) Values at Indicated Time Points

Vital sign measurements including SBP and DBP were taken in a supine position after at least 5 minutes of rest at Day -1, Day 1, Day 2 and Day 3 in each treatment period. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionMillimeters of mercury (mmHg) (Mean)
SBP; P1; Day-1; 12 hour pre-dose; n=21,21SBP; P1; Day1; 1 hour post-dose; n= 21, 21SBP; P1; Day1; 1.5 hour pre-dose; n= 21, 21SBP; P1; Day1; 2 hour post-dose; n= 21, 21SBP: P1; Day1; 4 hour post-dose; n= 21, 21SBP; P1; Day1; 6 hour post-dose; n= 21, 21SBP; P1; Day1; 8 hour post-dose; n= 21, 21SBP; P1; Day2; 24 hour post-dose; n= 21, 21SBP; P1; Day3; 48 hour post-dose; n= 21, 20SBP; P2; Day-1; 12 hour pre-dose; n= 19, 19SBP; P2; Day1; 1 hour post-dose; n= 19, 19SBP; P2; Day1; 1.5 hour post-dose; n= 19, 19SBP; P2; Day1; 2 hour post-dose; n= 19, 19SBP: P2; Day1; 4 hour post-dose; n= 19, 19SBP: P2; Day1; 6 hour post-dose; n= 19, 19SBP: P2; Day1; 8 hour post-dose; n= 19, 19SBP: P2; Day2; 24 hour post-dose; n= 19, 19SBP; P2; Day3; 48 hour post-dose; n= 18, 19DBP; P1; Day-1; 12 hour pre-dose; n= 21, 21DBP; P1; Day1; 1 hour post-dose; n= 21, 21DBP: P1; Day1; 1.5 hour post-dose; n= 21, 21DBP; P1; Day1; 2 hour post-dose; n= 21, 21DBP: P1; Day1; 4 hour post-dose; n= 21, 21DBP; P1; Day1; 6 hour post-dose; n= 21, 21DBP; P1; Day1; 8 hour post-dose; n= 21, 21DBP: P1; Day2; 24 hour post-dose; n= 21, 21DBP: P1; Day3; 48 hour post-dose; n= 21, 20DBP; P2; Day-1; 12 hour post-dose; n= 19, 19DBP; P2; Day1; 1 hour post-dose; n= 19, 19DBP; P2; Day1; 1.5 hour post-dose; n= 19, 19DBP; P2; Day1; 2 hour post-dose; n= 19, 19DBP; P2; Day1; 4 hour post-dose; n= 19, 19DBP: P2; Day1; 6 hour post-dose; n= 19, 19DBP; P2; Day1; 8 hour post-dose; n= 19, 19DBP: P2; Day2; 24 hour post-dose; n= 19, 19DBP: P2; Day3; 48 hour post-dose; n= 18, 19
Treatment A115.9112.8111.5113.3112.5110.9113.0111.4114.5113.8110.0108.9109.6109.5108.5109.8109.1112.965.463.764.063.464.861.463.064.967.363.163.961.162.562.859.461.162.965.9
Treatment B115.8111.6110.8112.6114.0113.0111.8110.5113.8116.2113.7112.2113.8113.5112.4111.5110.6116.564.963.563.965.764.462.763.764.266.065.864.163.465.365.361.562.964.467.2

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Terminal Phase Half-life (T1/2) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma

Blood samples were collected at indicated time points under fasting conditions for PK analysis of hydrochlorothiazide and amiloride. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Pre-dose, 0.33, 0.67, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10, 12,14, 16 hours post-dose on Day 1, 24 and 36 hours post dose on Day 2 and 48 hours post-dose on Day 3

,
InterventionHour (Median)
Hydrochlorothiazide; n= 37, 38Amiloride; n= 22, 22
Treatment A12.415.2
Treatment B11.316.6

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Maximum Observed Concentration (Cmax) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma

Blood samples were collected at indicated time points under fasting conditions for pharmacokinetic (PK) analysis of hydrochlorothiazide and amiloride. Bioequivalence of test product and reference product was assessed based on the 90 percent CIs for estimates of the geometric mean ratios between the Cmax of the test and reference products in relation to the conventional bioequivalence range. An analysis of variance was used with sequence, subject (sequence), treatment and period as fixed effects. (NCT03031496)
Timeframe: Pre-dose, 0.33, 0.67, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10, 12,14, 16 hours post-dose on Day 1, 24 and 36 hours post dose on Day 2 and 48 hours post-dose on Day 3

,
Interventionng/mL (Geometric Mean)
HydrochlorothiazideAmiloride
Treatment A3129.27
Treatment B3778.92

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Time of Occurrence of Cmax (Tmax) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma

Blood samples were collected at indicated time points under fasting conditions for PK analysis of hydrochlorothiazide and amiloride. Median and full range has been presented. (NCT03031496)
Timeframe: Pre-dose, 0.33, 0.67, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10, 12,14, 16 hours post-dose on Day 1, 24 and 36 hours post dose on Day 2 and 48 hours post-dose on Day 3

,
InterventionHour (Median)
HydrochlorothiazideAmiloride
Treatment A2.5052.507
Treatment B1.5092.508

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Total Protein Levels at Indicated Time Points

Serum total protein levels were assessed as a clinical chemistry laboratory parameter at Day -1 and Day 3 in each treatment period. Only those participants available at the specified time points were analyzed (represented by n=X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionGrams per liter (g/L) (Mean)
P1; Day-1; 24 hours pre-dose; n= 21, 21P1; Day 3; 48 hours post-dose; n= 21, 20P2; Day-1; 24 hours pre-dose; n= 19, 19P2; Day 3; 48 hours post-dose; n= 19, 19
Treatment A74.0874.5371.2973.56
Treatment B76.0674.9970.0672.33

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AUC From Time Zero to Infinity (AUC[0-inf]) of Hydrochlorothiazide and Amiloride Hydrochloride in Plasma

Blood samples were collected at indicated time points under fasting conditions for PK analysis of hydrochlorothiazide and amiloride. Bioequivalence of test product and reference product was assessed based on the 90 percent CIs for estimates of the geometric mean ratios between the AUC (0-inf) of the test and reference products in relation to the conventional bioequivalence range. An analysis of variance was used with sequence, subject (sequence), treatment and period as fixed effects. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles). (NCT03031496)
Timeframe: Pre-dose, 0.33, 0.67, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10, 12,14, 16 hours post-dose on Day 1, 24 and 36 hours post dose on Day 2 and 48 hours post-dose on Day 3

,
Interventionh*ng/mL (Geometric Mean)
Hydrochlorothiazide; n= 37, 38Amiloride; n= 22, 22
Treatment A2310117
Treatment B2490112

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Area Under the Curve (AUC) From Time Zero to the Time of the Last Quantifiable Concentration (AUC [0-t]) of Hydrochlorothiazide and Amiloride Hydrochloride

Blood samples were collected at indicated time points under fasting conditions for pharmacokinetic (PK) analysis of hydrochlorothiazide and amiloride. Bioequivalence of test product and reference product was assessed based on the 90 percent confidence intervals (CIs) for estimates of the geometric mean ratios between the AUC (0-t) of the test and reference products in relation to the conventional bioequivalence range. An analysis of variance was used with sequence, subject (sequence), treatment and period as fixed effects. (NCT03031496)
Timeframe: Pre-dose, 0.33, 0.67, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 6.0, 7.0, 8.0, 10, 12,14, 16 hours post-dose on Day 1, 24 and 36 hours post dose on Day 2 and 48 hours post-dose on Day 3

,
InterventionHour x nanograms/milliliter (h*ng/mL) (Geometric Mean)
HydrochlorothiazideAmiloride
Treatment A216096.3
Treatment B236094.1

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Alanine Aminotransferase (ALT), Alkaline Phosphatase (Alk.Phosph.) and Aspartate Aminotransferase (AST) Levels at Indicated Time Points

Serum ALT, alk. phosph. and AST levels were assessed as a clinical chemistry laboratory parameter at Day -1 and Day 3 in each treatment period. Only those participants available at the specified time points were analyzed (represented by n=X in the category titles). (NCT03031496)
Timeframe: Day -1 and Day 3 of each treatment period

,
InterventionUnit per liter (U/L) (Mean)
ALT;Period 1 (P1);Day -1;24 hour pre-dose;n=21,21ALT; P1; Day 3; 48 hour post-dose; n= 21,20ALT; P2; Day -1; 24 hour pre-dose; n= 19,19ALT; P2; Day 3; 48 hour post-dose; n= 19, 19Alk.phosph.; P1; Day -1; 24 hour pre-dose; n=21,21Alk.phosph.; P1; Day 3; 48 hour post-dose; n=21,20Alk.phosph.; P2; Day -1; 24 hour pre-dose; n=19,19Alk.phosph.; P2; Day 3; 48 hour post-dose; n=19,19AST; P1; Day -1; 24 hour pre-dose; n=21, 21AST; P1; Day 3; 48 hour post-dose; n=21, 20AST; P2; Day -1; 24 hour pre-dose; n=19, 19AST; P2; Day 3; 48 hour post-dose; n=19, 19
Treatment A19.815.915.815.867.567.165.166.821.917.521.619.9
Treatment B16.614.117.616.971.169.963.665.220.117.821.118.4

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Number of Participants Who Reported That Side Effects From Medication Led Them to Discontinue Medication

(NCT03461003)
Timeframe: from baseline to 6 months

InterventionParticipants (Count of Participants)
NICHE Method0
Usual Care3

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Number of Participants Who Self-reported Adherence to Intervention

Adherence is reported as the number of participants who self-reported at the 6-month visit that they had not missed any doses of their medication in the preceding month. (NCT03461003)
Timeframe: from month 5 to month 6

InterventionParticipants (Count of Participants)
NICHE Method5
Usual Care6

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Patient Satisfaction With Intervention as Assessed by a Survey

Patient satisfaction is scored from 0 to 10, where 0 is the worst health care possible and 10 is the best health care possible. (NCT03461003)
Timeframe: 6 months

Interventionscore on a scale (Mean)
NICHE Method9.929
Usual Care9.667

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Change in Mean 24-hour Ambulatory Systolic Blood Pressure

To assess 24-hour mean ambulatory blood pressure, participants wear a 24-hour blood pressure monitor, which records blood pressure at regular intervals throughout a 24-hour period, while awake and while asleep. The mean of all recordings over the 24-hour period is calculated per participant for both baseline and 6 months, and then the mean 24-hour systolic blood pressure at 6 months minus the mean 24-hour systolic blood pressure at baseline is calculated per participant. The average difference is reported, with a negative value indicating a reduction in blood pressure over time. (NCT03461003)
Timeframe: baseline, 6 months

InterventionmmHg (Mean)
NICHE Method-10.6
Usual Care-5.1

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Change in Mean Wake Ambulatory Systolic Blood Pressure

To assess mean wake ambulatory blood pressure, participants wear a 24-hour blood pressure monitor, which records blood pressure at regular intervals throughout a 24 hour period, throughout wake and sleep. The mean of all recordings that occur while the participant is awake during the 24-hour period is calculated for both baseline and 6 months, and then the mean wake systolic blood pressure at 6 months minus the mean wake systolic blood pressure at baseline is calculated per participant. The average difference is reported, with a negative value indicating a reduction in blood pressure over time. (NCT03461003)
Timeframe: baseline, 6 months

InterventionmmHg (Mean)
NICHE Method-10.5
Usual Care-6.2

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