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bismuth

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Occurs in Manufacturing Related Drugs Related Conditions Protein Interactions Research Growth

Description

Bismuth: A metallic element that has the atomic symbol Bi, and atomic number 83. Its principal isotope is Bismuth 209. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5359367
CHEBI ID33301
MeSH IDM0002611

Synonyms (153)

Synonym
AKOS015832970
bi
bismuth
bismut
bismuto
bismuth atom
wismut
83bi
CHEBI:33301
7440-69-9
bismuth, pieces, 1-12 mm, 99.999% trace metals basis
bismuth, beads, 1-5 mm, 99.999% trace metals basis
bismuth, powder, -100 mesh, >=99.999%
bismuth, powder, -100 mesh, >=99.99% trace metals basis
bismuth, shot, 4-30 mesh, 99.9% trace metals basis
bismuth, powder, -100 mesh, 99% trace metals basis
bismuth, granular, >=99.99% trace metals basis
bdbm85242
nsc_26947
cas_14882-18-9
FT-0623124
bismuth (lump)
bismuth ingot/button, ca. 36mm (1.4in) dia x 8mm (0.3in) thick
JCXGWMGPZLAOME-UHFFFAOYSA-N
bismuth, granular
bismuth pieces, 10cm (3.9in) & down
bismuth shot, spherical, 1-2mm (0.04-0.20in), low oxide
bismuth granules, 1-2mm (0.04-0.08in)
bismuth needles, 1-5cm (0.4-2in) long
bismuth powder, -100 mesh
bismuth rod, 12.7mm (0.5in) dia
bismuth powder, -200 mesh
bismuth foil, 1.0mm (0.04in) thick
bismuth, plasma standard solution, specpure?, bi 10,000?g/ml
bismuth, plasma standard solution, specpure?, bi 1000?g/ml
bismuth, aas standard solution, specpure?, bi 1000?g/ml
bismuth rod, 11mm (0.43in) dia
bismuth foil, 2.0mm (0.08in) thick
bismuth powder, -325 mesh
bismuth polycrystalline lump, puratronic?
bismuth needles
bismuth standard for aas, ready-to-use, traceable to bam, in nitric acid
bismuth powder
mfcd00134033
bismuth shot, elongated
bismuth granules
bismuth rod
bismuth pieces
bismuth standard for icp, for icp, ready-to-use, traceable to bam, in nitric acid
bismuth, shot, 99.9999%
bismuth, pieces, elongated, 99.999%
bismuth, foil, 50x50mm, thickness 2.0mm, 100%
bismuth, rod, 70mm, diameter 10.0mm, cast sticks, 100%
bismuth, powder, max. particle size 150 micron, weight 100 g, high purity 99.999%
bismuth, foil, thickness 0.007 mm, size 25 x 25 mm, purity 99.97%
bismuth, lump, 7 mm max. lump size, weight 50 g, purity 99.999%
bismuth, powder, 150 max. part. size (micron), weight 50 g, high purity 99.999%
bismuth, foil, thickness 0.004 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, thickness 3.0 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, thickness 0.03 mm, size 25 x 25 mm, purity 99.97%
bismuth, foil, 25x25mm, thickness 2.0mm, 100%
bismuth, foil, thickness 0.03 mm, size 50 x 50 mm, purity 99.97%
bismuth, powder, max. particle size 150 micron, weight 50 g, high purity 99.997%
bismuth, foil, 50x50mm, thickness 0.5mm, 100%
bismuth, foil, thickness 0.008 mm, purity 99.97%, size 25 x 25 mm
bismuth, foil, thickness 0.045 mm, size 150 x 150 mm, purity 99.97%
bismuth, powder, max. particle size 150 micron, weight 200 g, high purity 99.999%
bismuth, powder, max. particle size 45 micron, weight 200 g, purity 99.5+%
bismuth, lump, 10 mm max. lump size, weight 50 g, purity 99.999%
bismuth, foil, 25x25mm, thickness 0.25mm, 100%
bismuth, lump, 25 mm max. lump size, weight 100 g, high purity 99.9999%
bismuth, lump, 25 mm max. lump size, weight 50 g, high purity 99.9999%
bismuth, foil, 50x50mm, thickness 1.0mm, 99.97%
bismuth, powder, max. particle size 45 micron, weight 50 g, purity 99.5+%
bismuth, foil, thickness 0.006 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, thickness 0.007 mm, size 50 x 50 mm, purity 99.97%
bismuth, powder, 150 max. part. size (micron), weight 50 g, purity 99.97%
bismuth, foil, thickness 0.03 mm, purity 99.97%, size 50 x 50 mm
bismuth, rod, 140mm, diameter 10.0mm, cast sticks, 100%
bismuth, foil, size 100 x 100 mm, thickness 0.0125 mm, purity 99.97%
bismuth, lump, 25 mm max. lump size, weight 200 g, high purity 99.9999%
bismuth, powder, 150 max. part. size (micron), high purity 99.998%, weight 100 g
bismuth, foil, thickness 0.0125 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, thickness 0.04 mm, size 150 x 150 mm, purity 99.97%
bismuth, foil, thickness 0.04 mm, size 50 x 50 mm, purity 99.97%
bismuth, lump, 100 mm max. lump size, weight 2252 g, purity 99.999%
bismuth, foil, thickness 0.045 mm, size 25 x 25 mm, purity 99.97%
bismuth, lump, 25 mm max. lump size, weight 20 g, high purity 99.9999%
bismuth, foil, 25x25mm, thickness 1.0mm, 99.97%
bismuth, lump, 7 mm max. lump size, weight 100 g, purity 99.999%
bismuth, foil, 50x50mm, thickness 0.25mm, 100%
bismuth, powder, max. particle size 150 micron, weight 200 g, high purity 99.997%
bismuth, foil, 50x50mm, thickness 1.0mm, 100%
bismuth, foil, thickness 0.006 mm, size 25 x 25 mm, purity 99.97%
bismuth, powder, max. particle size 150 micron, weight 200 g, purity 99.97%
bismuth, foil, thickness 0.04 mm, size 100 x 100 mm, purity 99.97%
bismuth, lump, 10 mm max. lump size, weight 100 g, purity 99.999%
bismuth, foil, thickness 0.04 mm, size 25 x 25 mm, purity 99.97%
bismuth, foil, thickness 0.03 mm, size 150 x 150 mm, purity 99.97%
bismuth, foil, thickness 0.003 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, 25x25mm, thickness 1.0mm, 100%
bismuth, foil, thickness 0.045 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, thickness 0.009 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, thickness 0.03 mm, size 100 x 100 mm, purity 99.97%
bismuth, powder, max. particle size 150 micron, weight 100 g, purity 99.97%
bismuth, foil, thickness 0.003 mm, size 25 x 25 mm, purity 99.97%
bismuth, powder, max. particle size 45 micron, weight 100 g, purity 99.5+%
bismuth, foil, thickness 0.004 mm, size 25 x 25 mm, purity 99.97%
bismuth, lump, 10 mm max. lump size, weight 200 g, purity 99.999%
bismuth, foil, thickness 0.009 mm, size 25 x 25 mm, purity 99.97%
bismuth, foil, thickness 0.045 mm, size 100 x 100 mm, purity 99.97%
bismuth, lump, 7 mm max. lump size, weight 200 g, purity 99.999%
bismuth, lump, 100 mm max. lump size, weight 1126 g, purity 99.999%
bismuth, rod, 120mm, diameter 10.0mm, cast sticks, 100%
bismuth, foil, thickness 0.0125 mm, size 25 x 25 mm, purity 99.97%
bismuth, foil, thickness 0.008 mm, size 50 x 50 mm, purity 99.97%
bismuth, foil, 25x25mm, thickness 0.5mm, 100%
bismuth, 99.9%
DTXSID3052484
bismuthide
Q4918361
bi3 (b6 o13 (o h))
bi (b4 o6 (o h)2) (o h)
bismuth single crystal disc, 10mm (0.39in) dia, 1-3mm (0.04-0.1in) thick
bismuth single crystal disc, 10mm (0.39in) dia, 1-3mm (0.04-0.1in) thick, (111) orientation, polished both sides
bismuth single crystal disc, 10mm (0.39in) dia, 1-3mm (0.04-0.1in) thick, (100) orientation, polished both sides
bismuth single crystal, 15mm (0.59in) dia, 25mm (1in) long, (100) orientation
bismuth single crystal, 15mm (0.59in) dia, 25mm (1in) long, random orientation
Q942
bismuth, ingot, 99.9999% (6n), diameter 8 mm, length 42 mm, approx. 21 g
bismuth nanorods
bismuth sputtering target
bismuth nanopowder
bismuth nanorods properties
bismuth nanoprisms
bismuth metal
bismuth hollow cathode lamp: 2.0 diameter, 9-pin, non-coded
bismuth hollow cathode lamp: 2.0 diameter, 4-pin, cableless
bismuth hollow cathode lamp: 1.5 diameter, 2-pin, non-coded
bismuth standard: bi @ 10 microg/ml in 2% hno3
sulfur-free bismuth standard: bi @ 1000 microg/g in hydrocarbon oil
bismuth standard: bi @ 10000 microg/ml in 5% hno3
icp-ms internal standard: bi @ 100 ug/ml in 2% hno3
bismuth, elemental;
bismuth internal standard: bi @ 0.793 g/l in mineral oil
bismuth standard: bi @ 1000 microg/ml in 5% hno3
sulfur-free bismuth standard: bi @ 5000 microg/g in hydrocarbon oil
bismuth internal standard: bi @ 10 microg/ml in 2% hno3
bismuth aa standard: bi @ 1000 microg/ml in 5% hno3
bismuth standard: bi @ 1000 microg/g in hydrocarbon oil
bismuth internal standard in mineral oil - bi @ 0.793 g/l
bismuth - bi @ 1000 microg/g in hydrocarbon oil
bismuth - bi @ 1000 microg/ml in 5% hno3

Research Excerpts

Toxicity

Fourteen-day HDDT is non-inferior to bismuth-containing quadruple therapy, with fewer adverse effects and good treatment compliance, suggesting HDDT as an alternative for H.I.V.

ExcerptReferenceRelevance
" Bismuth blood and urine levels obtained from patients after administration of a new anti-ulcer drug (Bicitropeptide) in a well controlled clinical trial are discussed and suggest that that this bismuth containing drug behaves pharmacologically in a manner similar to the inorganic bismuth salts in man, low bismuth blood levels and the absence of toxic side effects being conspicuous features of the drug."( Bismuth toxicity in man II. Review of bismuth blood and urine levels in patients after administration of therapeutic bismuth formulations in relation to the problem of bismuth toxicity in man.
Mekel, R; Serfontein, WJ, 1979
)
0.26
" Changes in cell growth, cell viability, and the visual appearance of cells were used for the assessment of toxic response."( Cytotoxicity evaluation of a new radiopaque resin additive--triphenyl bismuth.
Bhagat, HR; Cabasso, I; Cardenas, HL; Marshall, MV; Rawls, HR, 1992
)
0.28
" Since 1980, five papers have addressed questions concerning potential metal toxicity, safe shop practices, measurement of airborne vapors and metal particulates, and the results of biological testing of personnel fabricating secondary field shaping blocks."( The safety of low melting point bismuth/lead alloys: a review.
Glasgow, GP, 1991
)
0.28
" During 12 months of follow-up, no side-effects were reported by TDB-treated patients, blood bismuth levels did not rise above discontinuation threshold concentrations (greater than 50 micrograms/L in the first 6 months, or greater than 100 micrograms/L in the second 6 months), and there were no adverse effects on haematological or biochemical indices."( The safety and efficacy of tripotassium dicitrato bismuthate (De-Nol) maintenance therapy in patients with duodenal ulceration.
Dunk, AA; Mowat, NA; O'Morain, C; Prabhu, U; Tobin, A, 1990
)
0.28
"The effect of preinduction of metallonthionein (MT) by bismuth subnitrate (BSN) on the adverse effects and antitumor activity of gamma-ray irradiation was investigated in mice."( Prevention of adverse effects of gamma-ray irradiation after metallothionein induction by bismuth subnitrate in mice.
Imura, N; Kawamura, E; Matsuzaki, N; Miura, N; Naganuma, A; Satoh, M, 1989
)
0.28
" A number of toxic effects have been attributed to bismuth compounds in humans: nephropathy, encephalopathy, osteoarthropathy, gingivitis, stomatitis and colitis."( Pharmacokinetics and toxicity of bismuth compounds.
de Wolff, FA; Slikkerveer, A,
)
0.13
"The effect of preinduction of metallothionein (MT) by bismuth (Bi) compounds on the toxic side effects and antitumor activity of adriamycin (ADR) was investigated in mice."( Specific reduction of toxic side effects of adriamycin by induction of metallothionein in mice.
Imura, N; Naganuma, A; Satoh, M, 1988
)
0.27
" The use of such therapies, however, may be impeded by a number of major disadvantages, including reduced patient compliance, the incidence of adverse events and primary or acquired antibiotic resistance."( Compliance, adverse events and antibiotic resistance in Helicobacter pylori treatment.
Malfertheiner, P, 1993
)
0.29
"The toxic effects of modified endodontic sealers, Fillcanal, N-Rickert, FS, and Sealer 26, were assessed."( Cytotoxicity of some modified root canal sealers and their leachable components.
Araki, K; Barbosa, SV; Spångberg, LS, 1993
)
0.29
" Adverse reactions to these agents are mild, transient and infrequent, and reports of serious adverse reactions are rare."( Review article: safety of bismuth in the treatment of gastrointestinal diseases.
Dixon, JS; Drake, FM; Tillman, LA; Wood, JR, 1996
)
0.29
" No adverse events were specifically attributed to ranitidine bismuth citrate."( The safety and efficacy of ranitidine bismuth citrate in combination with antibiotics for the eradication of Helicobacter pylori.
Bardhan, KD; Buckley, MJ; De Koster, EH; Duggan, AE; Gilvarry, J; Gummett, PA; Logan, RP; O'Morain, CA; Pounder, RE; Rauws, EA; Schaufelberger, HD; Wyeth, JW, 1996
)
0.29
" Twenty-four patients experienced side-effects, but in only seven cases was treatment discontinued due to adverse events."( Efficacy and safety of three 7-day Helicobacter pylori eradication regimens containing ranitidine bismuth citrate.
Bazzoli, F; Cannizzaro, O; D'Angelo, A; Ederle, A; Fossi, S; Gerace, G; Iaquinto, G; Olivieri, A; Pozzato, P; Reina, G; Ricciardiello, L; Roda, E; Scarpulla, G; Spadaccini, A; Tosatto, R; Zagari, M, 1998
)
0.3
" Three novel RBC-based triple therapies proved to be safe and well tolerated, with discontinuations due to side-effects occurring in less than 5% of cases."( Efficacy and safety of three 7-day Helicobacter pylori eradication regimens containing ranitidine bismuth citrate.
Bazzoli, F; Cannizzaro, O; D'Angelo, A; Ederle, A; Fossi, S; Gerace, G; Iaquinto, G; Olivieri, A; Pozzato, P; Reina, G; Ricciardiello, L; Roda, E; Scarpulla, G; Spadaccini, A; Tosatto, R; Zagari, M, 1998
)
0.3
" AH26 had a severe cytotoxic effect whilst Topseal and AH-Plus showed a markedly lower toxic influence on the cells during the experimental period."( Cytotoxicity of three resin-based root canal sealers: an in vitro evaluation.
Beltes, P; Geromichalos, GD; Kortsaris, AH; Koulaouzidou, EA; Papazisis, KT, 1998
)
0.3
"The kidney, in particular the proximal convoluted tubule, is a major target site for the toxic effects of various metals."( Exposure of cultured human proximal tubular cells to cadmium, mercury, zinc and bismuth: toxicity and metallothionein induction.
Hawksworth, GM; Jenner, W; Miles, AT; Rodilla, V, 1998
)
0.3
" The results obtained in this study showed the high cytotoxcity of the new AH Plus root canal sealer, which was shown to be equally or more toxic to the standard AH26 and Diaket materials."( Cytotoxic effect of four root filling materials.
Anić, I; Karlović, Z; Marsan, T; Miletić, I; Osmak, M; Pezelj-Ribarić, S, 2000
)
0.31
" Calcium hydroxide-based sealer was the least toxic sealer amongst the chemicals tested in both cultures."( Cytotoxicity of resin-, zinc oxide-eugenol-, and calcium hydroxide-based root canal sealers on human periodontal ligament cells and permanent V79 cells.
Chang, YC; Chou, MY; Huang, FM; Tai, KW, 2002
)
0.31
"The effect of tissue specific induction of metallothionein (MT) by preadministration of metal compounds on the antitumor activity and adverse effects of adriamycin (ADR) was examined using mice bearing colon 38 adenocarcinoma."( Modulation of adriamycin toxicity by tissue-specific induction of metallothionein synthesis in mice.
Imura, N; Naganuma, A; Satoh, M, 2000
)
0.31
" AH Plus was also shown to be toxic in concentrations of 16."( Examination of cytotoxicity and mutagenicity of AH26 and AH Plus sealers.
Anić, I; Garaj-Vrhovac, V; Jukić, S; Miletić, I; Osmak, M; Zeljezić, D, 2003
)
0.32
" Since both BSN and citrate are used clinically as pharmaceuticals, the combination regimen of BSN and citrate may be readily applicable as a countermeasure against the adverse side effects of CDDP without affecting its antitumor activity."( Citrate enhances the protective effect of orally administered bismuth subnitrate against the nephrotoxicity of cis-diamminedichloroplatinum.
Himeno, S; Imura, N; Kondo, Y; Naganuma, A; Nishimura, T; Satoh, M, 2004
)
0.32
" Adherence and adverse events for quadruple therapy were similar to currently recommended triple therapies."( Meta-analysis: the efficacy, adverse events, and adherence related to first-line anti-Helicobacter pylori quadruple therapies.
Dickason, J; Fischbach, LA; van Zanten, S, 2004
)
0.32
"8, 4, 20 mg/kg to male Crj:CD(SD)IGS rats (SPF) by intratracheal intermittent administration once a week for thirteen weeks to investigate its potential toxic effects; especially for specific adverse effects and changes related to pre-neoplastic lesions."( A 13-week toxicity study of bismuth in rats by intratracheal intermittent administration.
Chiba, M; Nakashima, H; Okamoto, M; Omae, K; Sano, Y; Satoh, H; Serizawa, K; Shinohara, A, 2005
)
0.33
"The consumption and production of bismuth are increasing, however there is very little information about the direct toxic effect of bismuth."( Oral toxicity of bismuth in rat: single and 28-day repeated administration studies.
Chiba, M; Nakashima, H; Okamoto, M; Omae, K; Sano, Y; Satoh, H; Serizawa, K, 2005
)
0.33
" The general public may assume that over-the-counter products are safe because they do not require a prescription."( Salicylate toxicity associated with administration of Percy medicine in an infant.
Badillo, R; Hagemann, TM; Lewis, TV; McGoodwin, L; Schaeffer, S, 2006
)
0.33
" We also analyzed the cyto- and genotoxic effects of these compounds to investigate their toxic potential."( Methylated bismuth, but not bismuth citrate or bismuth glutathione, induces cyto- and genotoxic effects in human cells in vitro.
Dopp, E; Hartmann, LM; Hippler, J; Hirner, AV; Rabieh, S; Rettenmeier, AW; von Recklinghausen, U, 2008
)
0.35
" Total numbers of adverse events were recorded."( Adverse events with bismuth salts for Helicobacter pylori eradication: systematic review and meta-analysis.
Ford, AC; Giguere, M; Khan, M; Malfertheiner, P; Moayyedi, P; Santana, J, 2008
)
0.35
" There were no serious adverse events occurring with bismuth therapy."( Adverse events with bismuth salts for Helicobacter pylori eradication: systematic review and meta-analysis.
Ford, AC; Giguere, M; Khan, M; Malfertheiner, P; Moayyedi, P; Santana, J, 2008
)
0.35
"Bismuth for the treatment of H pylori is safe and well-tolerated."( Adverse events with bismuth salts for Helicobacter pylori eradication: systematic review and meta-analysis.
Ford, AC; Giguere, M; Khan, M; Malfertheiner, P; Moayyedi, P; Santana, J, 2008
)
0.35
" However, treatment with therapeutically effective activities of (177)Lu-d9MAb was not free of toxic side effects."( 177Lu-immunotherapy of experimental peritoneal carcinomatosis shows comparable effectiveness to 213Bi-immunotherapy, but causes toxicity not observed with 213Bi.
Beck, R; Bruchertseifer, F; Quintanilla-Martinez, L; Seidl, C; Senekowitsch-Schmidtke, R; Zöckler, C, 2011
)
0.37
"The therapeutic efficacy of (177)Lu-d9MAb conjugates in peritoneal carcinomatosis is impaired by toxic side effects."( 177Lu-immunotherapy of experimental peritoneal carcinomatosis shows comparable effectiveness to 213Bi-immunotherapy, but causes toxicity not observed with 213Bi.
Beck, R; Bruchertseifer, F; Quintanilla-Martinez, L; Seidl, C; Senekowitsch-Schmidtke, R; Zöckler, C, 2011
)
0.37
" Seventeen patients experienced mild adverse events."( Effectiveness and safety of repeated quadruple therapy in Helicobacter pylori infection after failure of second-line quadruple therapy: repeated quadruple therapy as a third-line therapy.
Choi, JH; Hyun, JJ; Jung, SW; Kim, JH; Kim, SY; Koo, JS; Kwon, BS; Lee, SK; Lee, SW; Park, JY; Yim, HJ, 2011
)
0.37
"A retrial of quadruple therapy before use of a third-line therapy may be safe and effective for patients who fail to respond to second-line quadruple therapy."( Effectiveness and safety of repeated quadruple therapy in Helicobacter pylori infection after failure of second-line quadruple therapy: repeated quadruple therapy as a third-line therapy.
Choi, JH; Hyun, JJ; Jung, SW; Kim, JH; Kim, SY; Koo, JS; Kwon, BS; Lee, SK; Lee, SW; Park, JY; Yim, HJ, 2011
)
0.37
" Safety and tolerability were assessed by adverse events, physical examination and serum biochemistry."( Safety and tolerability of bismuthyl ecabet suspension, a novel anti-ulcer agent, following single and multiple oral dose administration in healthy Chinese subjects.
Chen, A; Jiang, N; Meng, L; Ou, N; Shi, R; Tang, N; Wang, Y; Wu, D; Xu, K; Zhang, H; Zhang, P; Zhang, X, 2012
)
0.38
"In both the single- and multiple-dose studies, no severe adverse events were observed in any of the volunteers."( Safety and tolerability of bismuthyl ecabet suspension, a novel anti-ulcer agent, following single and multiple oral dose administration in healthy Chinese subjects.
Chen, A; Jiang, N; Meng, L; Ou, N; Shi, R; Tang, N; Wang, Y; Wu, D; Xu, K; Zhang, H; Zhang, P; Zhang, X, 2012
)
0.38
"Bismuthyl ecabet was shown to be safe and well tolerated in healthy Chinese subjects."( Safety and tolerability of bismuthyl ecabet suspension, a novel anti-ulcer agent, following single and multiple oral dose administration in healthy Chinese subjects.
Chen, A; Jiang, N; Meng, L; Ou, N; Shi, R; Tang, N; Wang, Y; Wu, D; Xu, K; Zhang, H; Zhang, P; Zhang, X, 2012
)
0.38
" The results show that bismuth nanoparticles are more toxic than most previously reported bismuth compounds."( In vitro cytotoxicity of surface modified bismuth nanoparticles.
Hossain, M; Luo, Y; Ma, L; Qiao, Y; Su, M; Wang, C, 2012
)
0.38
"To establish the efficiency and adverse effects of the addition of bismuth subsalicylate to triple eradication therapy for Helicobacter pylori infection."( [Addition of bismuth subsalicylate to triple eradication therapy for Helicobacter pylori infection: efficiency and adverse events].
Díaz Ferrer, J; Hinostroza Morales, D,
)
0.13
" The adverse events of both groups were: diarrhea (10."( [Addition of bismuth subsalicylate to triple eradication therapy for Helicobacter pylori infection: efficiency and adverse events].
Díaz Ferrer, J; Hinostroza Morales, D,
)
0.13
"5 µg/mL), whereas higher concentrations (5-100 µg/mL) of BiOCl-NSs could trigger toxic effects on HaCaT cells, with changes in cell morphology and impairment of intracellular structures (mitochondria and cytoskeleton)."( An in vitro study on the cytotoxicity of bismuth oxychloride nanosheets in human HaCaT keratinocytes.
Fan, C; Gao, X; Peng, S; Wang, Y; Zhang, X, 2015
)
0.42
" In addition, data on side effect profiles and patient compliance were collected."( Different bismuth-based therapies for eradicating Helicobacter pylori: Randomized clinical trial of efficacy and safety.
Gokcan, H; Onal, IK; Oztas, E, 2016
)
0.43
" The glycolate complexes are selectively toxic against parasite amastigotes, with all complexes being nontoxic towards promastigotes and human fibroblast cells."( Bismuth(III) α-hydroxy carboxylates: highly selective toxicity of glycolates towards Leishmania major.
Andrews, PC; Blair, VL; Kedzierski, L; Loh, A; Ong, YC, 2015
)
0.42
" Further investigations with the use of in vivo animal models are required to validate the potential adverse biological effects of TheraCal LC on hDPSCs."( Cytotoxicity and osteogenic potential of silicate calcium cements as potential protective materials for pulpal revascularization.
Bortoluzzi, EA; Cutler, CW; El-Awady, AR; Hammond, BD; Niu, LN; Palani, CD; Pashley, DH; Pei, DD; Tay, FR; Tian, FC, 2015
)
0.42
" In vitro cytotoxic activities against cancerous (human chronic myelogenous leukemia, K562 and murine metastatic melanoma, B16F10) and healthy non-cancerous (murine fibroblasts, L929 and murine melanocytes, Melan-A) cells showed that, compared to free ligands, both of the metal complexes are more active as anticancer agents at low concentration in cancerous cell lines, but also possessed toxic effect at comparatively higher concentration towards the non-cancerous cells."( Cytotoxicity and apoptotic activity of novel organobismuth(V) and organoantimony(V) complexes in different cancer cell lines.
Demicheli, C; Dittz, D; Frézard, F; Ishfaq, M; Islam, A; Marzano, IM; Paz Lopes, MT; Perreira-Maia, EC; Rodrigues, BL, 2016
)
0.43
" The absence of toxic effects on epithelial cells growing with BisBAL NPs was corroborated with long-time experiments (24-72 hrs."( Cytotoxic Effect of Lipophilic Bismuth Dimercaptopropanol Nanoparticles on Epithelial Cells.
Badireddy, AR; Chellam, S; Claudio, CR; Francisco, CC; Isela, SN; Israel, MG; José, MS; Rene, HD, 2016
)
0.43
"High-dose chemotherapy prior to autologous stem cell transplantation (ASCT) leads to adverse effects including mucositis, neutropenia and bacteremia."( Bismuth adjuvant ameliorates adverse effects of high-dose chemotherapy in patients with multiple myeloma and malignant lymphoma undergoing autologous stem cell transplantation: a randomised, double-blind, prospective pilot study.
Hansen, PB; Penkowa, M, 2017
)
0.46
"We show for the first time that bismuth significantly reduces grade 2 stomatitis, febrile neutropenia and infections caused by melphalan in multiple myeloma, where adverse effects also were significantly linked to gender."( Bismuth adjuvant ameliorates adverse effects of high-dose chemotherapy in patients with multiple myeloma and malignant lymphoma undergoing autologous stem cell transplantation: a randomised, double-blind, prospective pilot study.
Hansen, PB; Penkowa, M, 2017
)
0.46
" Efficacy (by intention to treat) was analyzed using the inverse variance method; safety data were recorded as the occurrence of any adverse event."( Efficacy and Safety of Quinolone-Containing Rescue Therapies After the Failure of Non-Bismuth Quadruple Treatments for Helicobacter pylori Eradication: Systematic Review and Meta-Analysis.
Gisbert, JP; Marin, AC; McNicholl, AG; Nyssen, OP, 2017
)
0.46
" Adverse events occurred in 55 patients (15."( Effectiveness and Safety of Pylera® in Patients Infected by Helicobacter Pylori: A Multicenter, Retrospective, Real Life Study.
Allegretta, L; Baldassarre, G; Brandimarte, G; Cassieri, C; De Bastiani, R; Di Mario, F; Elisei, W; Ferronato, A; Franceschi, M; Licci, C; Miraglia, C; Penna, A; Picchio, M; Pranzo, G; Rizzo, GL; Savarino, E; Scida, S; Tursi, A, 2018
)
0.48
" Due to the reported adverse events of bismuth on human health, we extended our studies on the mechanisms for BiNP induced nephrotoxicity."( The protective role of autophagy in nephrotoxicity induced by bismuth nanoparticles through AMPK/mTOR pathway.
Li, R; Liu, Y; Shi, H; Song, Z; Wang, Y; Yu, H; Zhang, LW; Zhang, X; Zhao, J, 2018
)
0.48
" Adverse events were reported by 32."( The "three-in-one" formulation of bismuth quadruple therapy for Helicobacter pylori eradication with or without probiotics supplementation: Efficacy and safety in daily clinical practice.
Bazzoli, F; Conigliaro, R; Eusebi, LH; Farinati, F; Grande, G; Gravina, AG; Ierardi, E; Maconi, G; Panarese, A; Romano, M; Romiti, A; Savarino, E; Stasi, E; Zagari, RM, 2018
)
0.48
" However, little is known regarding the toxic effects of surface-modified nZVI on multiple species in the ecosystem."( Impact of surface modification on the toxicity of zerovalent iron nanoparticles in aquatic and terrestrial organisms.
Chang, YS; Hwang, YS; Jang, MH; Pangging, M; Yoon, H, 2018
)
0.48
" Adverse events were recorded by patients in specially developed diaries."( Evaluation of the efficacy and safety of the hybrid scheme for eradication therapy of Helicobacter pylori infection.
Andreev, DN; Dicheva, DT; Maiev, IV; Partzvania-Vinogradova, EV; Yurenev, GL, 2018
)
0.48
" The incidence of adverse events with the use of triple, four-component and hybrid ET regimens was 15; 18."( Evaluation of the efficacy and safety of the hybrid scheme for eradication therapy of Helicobacter pylori infection.
Andreev, DN; Dicheva, DT; Maiev, IV; Partzvania-Vinogradova, EV; Yurenev, GL, 2018
)
0.48
" In this work, we reported a novel kind of BiOI@CuS nanoparticle to achieve safe and effective therapy of lung cancer by co-loading hydrochloric acid doxorubicin (DOX) and aspirin phenacetin and caffeine (APC)."( Construction of DOX/APC co-loaded BiOI@CuS NPs for safe and highly effective CT imaging and chemo-photothermal therapy of lung cancer.
Cheng, J; He, D; Huang, G; Li, W; Wang, R; Zhang, Y; Zhu, J, 2019
)
0.51
" Efficacy and treatment-related adverse events were assessed."( Non-bismuth and bismuth quadruple therapies based on previous clarithromycin exposure are as effective and safe in an area of high clarithromycin resistance: A real-life study.
Avallone, L; Bazzoli, F; Compare, D; Dallio, M; Federico, A; Granata, L; Gravina, AG; Loguercio, C; Martorano, M; Miranda, A; Mucherino, C; Nardone, G; Priadko, K; Romano, L; Romano, M; Romiti, A; Romito, MR; Sgambato, D; Tuccillo, C; Zagari, RM, 2020
)
0.56
" Adverse events occurred in 24."( Non-bismuth and bismuth quadruple therapies based on previous clarithromycin exposure are as effective and safe in an area of high clarithromycin resistance: A real-life study.
Avallone, L; Bazzoli, F; Compare, D; Dallio, M; Federico, A; Granata, L; Gravina, AG; Loguercio, C; Martorano, M; Miranda, A; Mucherino, C; Nardone, G; Priadko, K; Romano, L; Romano, M; Romiti, A; Romito, MR; Sgambato, D; Tuccillo, C; Zagari, RM, 2020
)
0.56
" As for adverse events, HDDT was significantly less than BQT and CT regardless of duration, while BQT for 14 days represented higher adverse events than ST, HT and CT ≥ 10."( Comparative efficacy and safety of high-dose dual therapy, bismuth-based quadruple therapy and non-bismuth quadruple therapies for Helicobacter pylori infection: a network meta-analysis.
Cheng, L; Feng, R; Ma, X; Su, Y; Wang, W; Xu, H; Yang, Y; Zhang, D, 2021
)
0.62
" This case highlights the potential adverse effects of over-the-counter medications."( Salicylate toxicity from chronic bismuth subsalicylate use.
Halani, S; Wu, PE, 2020
)
0.56
" The total incidence of adverse events during the eradication therapy did not significantly differ between the ACLA and LCLA groups (31."( Antofloxacin-based bismuth quadruple therapy is safe and effective in Helicobacter pylori eradication: A prospective, open-label, randomized trial.
He, XJ; Jiang, CS; Li, DZ; Liu, G; Wang, W; Zeng, XP, 2021
)
0.62
" The adverse events were predictable and reported as frequent adverse events during triple-antibiotic therapy."( Pharmacokinetic Interactions between Tegoprazan and Metronidazole/Tetracycline/Bismuth and Safety Assessment in Healthy Korean Male Subjects.
Jeon, JY; Kim, B; Kim, MG; Kim, SY; Lee, J; Moon, SJ; Oh, K; Song, GS, 2021
)
0.62
"The safety of Helicobacter pylori eradication treatments and to what extent adverse events (AEs) influence therapeutic compliance in clinical practice are hardly known."( Adverse Event Profile During the Treatment of Helicobacter pylori: A Real-World Experience of 22,000 Patients From the European Registry on H. pylori Management (Hp-EuReg).
Alekseenko, S; Areia, M; Barrio, J; Bordin, D; Bujanda, L; Buzas, GM; Caldas, M; Camarero, JG; Castro-Fernandez, M; Dekhnich, NN; Dominguez-Cajal, M; Fadeenko, G; Fernandez-Salazar, L; Georgopoulos, S; Gisbert, JP; Gomez Rodriguez, BJ; Heluwaert, F; Huguet, JM; Ilchishina, T; Jonaitis, L; Jurecic, NB; Kikec, Z; Kupcinskas, J; Lafuente, MR; Leja, M; Lerang, F; Lucendo, A; Machado, JC; Megraud, F; Modolell, I; Ntouli, V; Nuñez, O; Nyssen, OP; O'Morain, C; Ortuño, J; Pellicano, R; Perez-Aisa, A; Perez-Lasala, J; Perona, M; Phull, P; Puig, I; Rodrigo, L; Rokkas, T; Romero, PM; Shvets, O; Simsek, C; Simsek, I; Tepes, B; Tonkic, A; Venerito, M; Vologzhanina, L; Voynovan, I; Zaytsev, O, 2021
)
0.62
" Safety was assessed by adverse event monitoring, physical examinations, vital signs, 12-lead electrocardiograms and clinical laboratory tests."( Evaluation of safety and pharmacokinetics of bismuth-containing quadruple therapy with either vonoprazan or lansoprazole for Helicobacter pylori eradication.
Bhatia, S; Chung, H; Huh, KY; Kim, YK; Lee, S; Nakaya, R; Takanami, Y; Yu, KS, 2022
)
0.72
" Vonoprazan-containing quadruple therapy was safe and well tolerated."( Evaluation of safety and pharmacokinetics of bismuth-containing quadruple therapy with either vonoprazan or lansoprazole for Helicobacter pylori eradication.
Bhatia, S; Chung, H; Huh, KY; Kim, YK; Lee, S; Nakaya, R; Takanami, Y; Yu, KS, 2022
)
0.72
" Twenty-three children reported at least one adverse event (63."( Efficacy and safety of bismuth-based quadruple therapy for Helicobacter pylori eradication in children.
Bontems, P; Cadranel, S; Kotilea, K; Mahler, T; Miendje Deyi, VY; Nguyen, J; Salame, A; Verset, L, 2021
)
0.62
" pylori eradication in children is a safe and very effective solution, especially for previously treated patients and those infected with double resistant strains."( Efficacy and safety of bismuth-based quadruple therapy for Helicobacter pylori eradication in children.
Bontems, P; Cadranel, S; Kotilea, K; Mahler, T; Miendje Deyi, VY; Nguyen, J; Salame, A; Verset, L, 2021
)
0.62
" The secondary outcomes included symptom improvement, patient compliance, and incidence of adverse events."( The efficacy and safety of different bismuth agents in Helicobacter pylori first-line eradication: A multicenter, randomized, controlled clinical trial.
Cao, Y; Huo, L; Liu, J; Liu, Y; Lv, H; Qi, Y; Shi, Y; Wang, J; Wang, L; Wei, X; Zhang, J; Zhang, L, 2021
)
0.62
" There were also no significant differences in the symptom improvement rate, overall adverse reaction rate, or patient compliance among the 4 groups."( The efficacy and safety of different bismuth agents in Helicobacter pylori first-line eradication: A multicenter, randomized, controlled clinical trial.
Cao, Y; Huo, L; Liu, J; Liu, Y; Lv, H; Qi, Y; Shi, Y; Wang, J; Wang, L; Wei, X; Zhang, J; Zhang, L, 2021
)
0.62
" Adverse events were recorded during follow-up by telephone interview."( Efficacy and safety of bismuth quadruple regimens containing tetracycline or furazolidone for initial eradication of Helicobacter pylori.
Cao, Y; He, W; Li, X; Wang, J, 2021
)
0.62
"The clarithromycin-based triple therapy is the most prescribed Helicobacter pylori eradication regimen in Europe; it causes adverse effects in a significant proportion of subjects, leading to discontinuation."( Randomised clinical trial: comparison of efficacy and adverse effects of a standard triple clarithromycin-containing regimen with high-dose amoxicillin and bismuth therapy in Helicobacter pylori eradication.
Daugule, I; Leja, M; Lielause, A; Park, JY; Paršutins, S; Poļaka, I; Rūdule, A; Sjomina, O; Stonāns, I; Vangravs, R, 2022
)
0.72
"We compared the efficacy and spectrum of adverse effects of clarithromycin-based triple therapy with the high-dose amoxicillin/bismuth regimen."( Randomised clinical trial: comparison of efficacy and adverse effects of a standard triple clarithromycin-containing regimen with high-dose amoxicillin and bismuth therapy in Helicobacter pylori eradication.
Daugule, I; Leja, M; Lielause, A; Park, JY; Paršutins, S; Poļaka, I; Rūdule, A; Sjomina, O; Stonāns, I; Vangravs, R, 2022
)
0.72
"Information on treatment completion and adverse effects were collected via a telephone interview at 21-28 days after medication delivery."( Randomised clinical trial: comparison of efficacy and adverse effects of a standard triple clarithromycin-containing regimen with high-dose amoxicillin and bismuth therapy in Helicobacter pylori eradication.
Daugule, I; Leja, M; Lielause, A; Park, JY; Paršutins, S; Poļaka, I; Rūdule, A; Sjomina, O; Stonāns, I; Vangravs, R, 2022
)
0.72
"We analysed 483 subjects for adverse effects (248 vs."( Randomised clinical trial: comparison of efficacy and adverse effects of a standard triple clarithromycin-containing regimen with high-dose amoxicillin and bismuth therapy in Helicobacter pylori eradication.
Daugule, I; Leja, M; Lielause, A; Park, JY; Paršutins, S; Poļaka, I; Rūdule, A; Sjomina, O; Stonāns, I; Vangravs, R, 2022
)
0.72
"Bismuth-based high-dose amoxicillin therapy showed a lower efficacy but was less frequently associated with adverse effects."( Randomised clinical trial: comparison of efficacy and adverse effects of a standard triple clarithromycin-containing regimen with high-dose amoxicillin and bismuth therapy in Helicobacter pylori eradication.
Daugule, I; Leja, M; Lielause, A; Park, JY; Paršutins, S; Poļaka, I; Rūdule, A; Sjomina, O; Stonāns, I; Vangravs, R, 2022
)
0.72
" The secondary endpoints were adverse effects, symptom improvement rates, and patient compliance."( Efficacy and safety of high-dose esomeprazole-amoxicillin dual therapy for Helicobacter pylori rescue treatment: a multicenter, prospective, randomized, controlled trial.
Bi, H; Chen, X; Chen, Y; Han, S; Li, M; Lin, T; Liu, J; Lyu, T; Shi, Y; Wang, J; Wang, S; Yuan, D; Zhao, X, 2022
)
0.72
" The incidence of adverse events in the HDDT group was significantly lower than that in the TFEB group (11."( Efficacy and safety of high-dose esomeprazole-amoxicillin dual therapy for Helicobacter pylori rescue treatment: a multicenter, prospective, randomized, controlled trial.
Bi, H; Chen, X; Chen, Y; Han, S; Li, M; Lin, T; Liu, J; Lyu, T; Shi, Y; Wang, J; Wang, S; Yuan, D; Zhao, X, 2022
)
0.72
" The inclusion of Bifiform in the eradication scheme dramatically reduces the frequency of adverse events and increases patient compliance, and also maintains the protective factors of the gastrointestinal mucosa at a higher level."( [A prospective randomized comparative study of the efficacy and safety of a two-week bismuth-based quadrotherapy of
Iakovenko, AV; Ivanov, AN; Soluyanova, IP; Strokova, TV; Vasilyev, NN; Yakovenko, EP, 2021
)
0.62
" However, the large doses, short circulation time and adverse effects are the intrinsic limitations of CT contrast agents, preventing their extended and safe use in the clinical setting."( Bismuth nanomaterials as contrast agents for radiography and computed tomography imaging and their quality/safety considerations.
Guo, H; Wang, Y; Yu, H; Zhang, L, 2022
)
0.72
"PTBD is safe and effective in the management of biliary obstruction caused by PCCA."( Percutaneous transhepatic biliary drainage for biliary obstruction in perihilar cholangiocarcinoma: a 10-year analysis of safety and outcomes using the CCI index.
Ausania, F; Bermúdez, P; Burrel, M; Carrero, E; Fondevila, C; Gómez, FM; Hessheimer, A; Molina, V; Moreno, J; Páez-Carpio, A; Serrano, E; Zarco, FX, 2023
)
0.91
" pylori eradication rate, changes in clinical symptoms of epigastric pain scores, and the incidence of adverse reactions."( Efficacy and safety of bifidobacterium quadruple viable tablets in the treatment of Helicobacter pylori-infected peptic ulcer or gastritis patients: a systematic review and meta-analysis.
Chen, P; Jiang, X; Liu, B; Xu, C; Xu, Q; Zhang, L, 2023
)
0.91
" The improvement of clinical symptoms of patients is better than that of bismuth-containing quadruple therapy, and the incidence of adverse reactions is lower than that of bismuth-containing quadruple therapy."( Efficacy and safety of bifidobacterium quadruple viable tablets in the treatment of Helicobacter pylori-infected peptic ulcer or gastritis patients: a systematic review and meta-analysis.
Chen, P; Jiang, X; Liu, B; Xu, C; Xu, Q; Zhang, L, 2023
)
0.91
" The incidence of treatment-emergent adverse events was similar between the groups, with no serious adverse events."( Pharmacokinetics, Safety, and Tolerability of Vonoprazan- or Esomeprazole-Based Bismuth-Containing Quadruple Therapy: A Phase 1, Double-Blind, Parallel-Group Study in Adults with Helicobacter pylori Infection in China.
Czerniak, R; Gu, L; Hu, C; Men, R; Miao, J; Tang, J; Wang, W; Wang, Y; Yang, L; Yoshida, N, 2023
)
0.91
" The secondary outcomes were symptom improvement rate, patient compliance, and incidence of adverse events."( Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial.
Chen, S; Dong, Q; Liu, Y; Shen, W; Shi, Y, 2023
)
0.91
" In addition, the symptom improvement rate, overall adverse reaction rate, and patient compliance were similar among the three groups (P >0."( Efficacy and safety of triple therapy containing berberine, amoxicillin, and vonoprazan for Helicobacter pylori initial treatment: A randomized controlled trial.
Chen, S; Dong, Q; Liu, Y; Shen, W; Shi, Y, 2023
)
0.91
" •Drug adverse effects were fewer and milder in the gemifloxacin group."( EFFICACY AND SAFETY OF GEMIFLOXACIN CONTAINING TREATMENT REGIMEN IN FIRST-LINE TREATMENT OF HELICOBACTER PYLORI.
Alanli, R; Aydin, MF; Ergül, B; Kucukay, MB; Yakaryilmaz, F,
)
0.13
" pylori eradication and adverse events (AEs)."( Efficacy and safety of minocycline quadruple therapy for Helicobacter pylori eradication: A meta-analysis of RCTs.
Gao, W; Wang, L; Yin, Y; Zhang, X; Zhu, M, 2023
)
0.91

Pharmacokinetics

The goal of this study was to evaluate the pharmacokinetic interaction between tegoprazan and triple-antibiotic therapy containing metronidazole, tetracycline, and bismuth. The objective was to investigate the pharmacokeretic interaction of the novel PPI anaprazole, amoxicillin and clarithromycin with/without bistuth.

ExcerptReferenceRelevance
" a) In terms of the nephrotoxic factors, the Cmax of platinum did not increase dose-dependently, and total clearance of platinum was constant under the same time of injection; b) As for the antitumor effect, AUC of ultrafilterable (free) platinum increased dose-dependently."( [A method of cisplatin administration with the aid of high-dose bismuth subnitrate, and their pharmacokinetics].
Kawamura, E; Morikawa, T, 1989
)
0.28
" After the last dose the geometric mean for Cmax for 500 mg bid of GR122311X was 5 ng."( Comparative pharmacokinetics of bismuth from ranitidine bismuth citrate (GR122311X), a novel anti-ulcerant and tripotassium dicitrato bismuthate (TDB).
Frazer, NM; Keene, ON; Lacey, LF; Smith, JT, 1994
)
0.29
"We investigated the hypothesis that distributions of continuous pharmacokinetic variables are positively skewed in nature and that logarithmic transformation of these variables restores normality."( Common noncompartmental pharmacokinetic variables: are they normally or log-normally distributed?
Bye, A; Keene, ON; Lacey, LF; Pritchard, JF, 1997
)
0.3
" The non-compartmental method was used for pharmacokinetic analysis."( Pharmacokinetics and bioequivalence of ranitidine and bismuth derived from two compound preparations.
Jiang, B; Ruan, ZR; Xu, DH; Yuan, H; Zhou, Q, 2006
)
0.33
"Various pharmacokinetic parameters of ranitidine derived from the two compound preparations, including C(max), AUC( (0-t)), AUC( (0-infinity)), T(max) and T((1/2)), were nearly consistent with previous observations."( Pharmacokinetics and bioequivalence of ranitidine and bismuth derived from two compound preparations.
Jiang, B; Ruan, ZR; Xu, DH; Yuan, H; Zhou, Q, 2006
)
0.33
" The mice were sacrificed at different time points for pharmacokinetic studies."( Pharmacokinetics and toxicity of (213)Bi-labeled PAI2 in preclinical targeted alpha therapy for cancer.
Abbas Rizvi, SM; Allen, BJ; Apostolidis, C; Brechbiel, MW; Morgenstern, A; Qu, CF; Raja, C; Song, EY, 2007
)
0.34
" The goal of this study was to evaluate the pharmacokinetic interaction between tegoprazan and triple-antibiotic therapy containing metronidazole, tetracycline, and bismuth."( Pharmacokinetic Interactions between Tegoprazan and Metronidazole/Tetracycline/Bismuth and Safety Assessment in Healthy Korean Male Subjects.
Jeon, JY; Kim, B; Kim, MG; Kim, SY; Lee, J; Moon, SJ; Oh, K; Song, GS, 2021
)
0.62
" Pharmacokinetic blood samples were collected within 24 h after the last dose."( Pharmacokinetic Interactions between Tegoprazan and Metronidazole/Tetracycline/Bismuth and Safety Assessment in Healthy Korean Male Subjects.
Jeon, JY; Kim, B; Kim, MG; Kim, SY; Lee, J; Moon, SJ; Oh, K; Song, GS, 2021
)
0.62
"Eleven cohort 1 subjects and ten cohort 2 subjects were included in the pharmacokinetic analysis."( Pharmacokinetic Interactions between Tegoprazan and Metronidazole/Tetracycline/Bismuth and Safety Assessment in Healthy Korean Male Subjects.
Jeon, JY; Kim, B; Kim, MG; Kim, SY; Lee, J; Moon, SJ; Oh, K; Song, GS, 2021
)
0.62
"Changes in the tegoprazan, tetracycline, and bismuth pharmacokinetic parameters were detected after concurrent administration."( Pharmacokinetic Interactions between Tegoprazan and Metronidazole/Tetracycline/Bismuth and Safety Assessment in Healthy Korean Male Subjects.
Jeon, JY; Kim, B; Kim, MG; Kim, SY; Lee, J; Moon, SJ; Oh, K; Song, GS, 2021
)
0.62
" The objective of this study was to investigate the pharmacokinetic interaction of the novel PPI anaprazole, amoxicillin and clarithromycin with/without bismuth."( Pharmacokinetic Interaction of Anaprazole, Amoxicillin and Clarithromycin after Single-Dose Simultaneous Administration and the Effect of Adding Bismuth on Their Pharmacokinetics in Healthy Male Chinese Subjects.
Chen, J; Ding, S; Li, T; Liu, Y; Shao, F; Wang, L; Xie, L; Zhang, Z; Zhou, C; Zhou, S; Zhu, B; Zhu, J, 2023
)
0.91
"This single-centre, randomised, open-label phase 1 pharmacokinetic study included healthy Chinese male participants, comprising two cohorts (cohort 1, 4 × 4 crossover design; cohort 2, 2 × 2 crossover design)."( Pharmacokinetic Interaction of Anaprazole, Amoxicillin and Clarithromycin after Single-Dose Simultaneous Administration and the Effect of Adding Bismuth on Their Pharmacokinetics in Healthy Male Chinese Subjects.
Chen, J; Ding, S; Li, T; Liu, Y; Shao, F; Wang, L; Xie, L; Zhang, Z; Zhou, C; Zhou, S; Zhu, B; Zhu, J, 2023
)
0.91

Compound-Compound Interactions

Dietary intervention combined with bismuth potassium citrate exhibited more effective treatment in Helicobacter pylori-related CAG. This suggests proper diet has a positive impact on improving the therapeutic efficacy of bismuth kpotassium citrate.

ExcerptReferenceRelevance
" A number of studies have now been undertaken using an acid inhibitor in combination with two antibiotics."( Eradication of Helicobacter pylori: omeprazole in combination with antibiotics.
Axon, AT; Moayyedi, P, 1996
)
0.29
"To test eradication and adverse events of ranitidine bismuth citrate (RBC) when given with metronidazole and either oxytetracycline or spiramycin."( Spiramycin is comparable to oxytetracycline in eradicating H. pylori when given with ranitidine bismuth citrate and metronidazole.
Bang, CJ; Berstad, A; Coll, P; Hatlebakk, JG; Hausken, T; Nysaeter, G; Olafsson, S; Olafsson, T; Tefera, S, 1999
)
0.3
" pylori eradication rate in both metronidazole-sensitive and -resistant strains following quadruple therapy using single-triple capsules of bismuth biskalcitrate, metronidazole and tetracycline, given with omeprazole."( Efficacy and safety of single-triple capsules of bismuth biskalcitrate, metronidazole and tetracycline, given with omeprazole, for the eradication of Helicobacter pylori: an international multicentre study.
Borody, T; Dallaire, C; De Boer, WA; Fallone, CA; Farley, A; Mégraud, F; O'Morain, C; Piotrowski, J; Schuman, R; Spénard, J; Tytgat, G, 2003
)
0.32
" Radioimmunotherapy was also combined with a single injection of 300 microg paclitaxel to explore improved efficacy."( Radioimmunotherapy with alpha-particle emitting 213Bi-C-functionalized trans-cyclohexyl-diethylenetriaminepentaacetic acid-humanized 3S193 is enhanced by combination with paclitaxel chemotherapy.
Brechbiel, MW; Kelly, MP; Lee, FT; Scott, AM; Smyth, FE; Tahtis, K, 2007
)
0.34
"To compare the short- and long-term sealing ability of root canal fillings consisting of AH-26 and laterally compacted gutta-percha in combination with a self-etching dentin bonding system and the Epiphany-Resilon system."( Long-term evaluation of the sealing ability of two root canal sealers in combination with self-etching bonding agents.
Economides, N; Gogos, C; Helvatjoglu-Antoniades, M; Kokorikos, I; Kolokouris, I, 2009
)
0.35
"The Epiphany-Resilon system and the group obturated with AH-26 sealer and gutta-percha, in combination with the self-etching bonding system after removal of the smear layer with EDTA, demonstrated similar sealing ability."( Long-term evaluation of the sealing ability of two root canal sealers in combination with self-etching bonding agents.
Economides, N; Gogos, C; Helvatjoglu-Antoniades, M; Kokorikos, I; Kolokouris, I, 2009
)
0.35
" The use of an ITS in combination with CL dry cow treatment was associated with significantly lower clinical and subclinical mastitis in the following lactation, with a greater difference found in cows that had a history of subclinical mastitis in the previous lactation."( The use of an internal teat sealant in combination with cloxacillin dry cow therapy for the prevention of clinical and subclinical mastitis in seasonal calving dairy cows.
Deighton, M; Malmo, J; Runciman, DJ, 2010
)
0.36
" The purpose of this study was to evaluate, in terms of both recurrence and the preservation of contour and function, the effectiveness of enucleation combined with peripheral ostectomy (Enu/PO) in managing large mandibular cystic ameloblastomas."( Enucleation combined with peripheral ostectomy: its role in the management of large cystic ameloblastomas of the mandible.
Fu, T; Liu, Y; Shan, Y; Shi, S; Zhao, S, 2014
)
0.4
" In summary, the method of multi-wavelength fingerprints combined with antioxidant activities has been proved to be a feasible and scientific procedure for monitoring and evaluating the quality consistency of CBAT."( Monitoring and evaluating the quality consistency of Compound Bismuth Aluminate tablets by a simple quantified ratio fingerprint method combined with simultaneous determination of five compounds and correlated with antioxidant activities.
Gao, J; Huang, J; Ling, J; Liu, Y; Liu, Z; Sun, G; Wang, Y, 2015
)
0.42
"To assess the efficacy and safety of omeprazole given with the new single capsule of bismuth, metronidazole and tetracycline (OBMT) compared with quadruple treatment consisting of omeprazole, bismuth, amoxicillin and clarithromycin (OBAC) for Helicobacter pylori eradication in duodenal ulcer patients."( New single capsule of bismuth, metronidazole and tetracycline given with omeprazole versus quadruple therapy consisting of bismuth, omeprazole, amoxicillin and clarithromycin for eradication of Helicobacter pylori in duodenal ulcer patients: a Chinese pro
Chen, Y; Du, Y; Li, Y; Liu, D; Lv, N; Pan, X; Wang, H; Wang, J; Wu, K; Xie, Y; Xu, J; Zeng, Z; Zhang, G, 2018
)
0.48
"The objective of this study was to investigate the therapeutic effect of transcatheter intra-arterial infusion of lecithin-modified Bi nanoparticles (Bi-Ln NPs) combined with interventional PTT (IPTT) on hepatocellular carcinoma."( Transcatheter Intra-Arterial Infusion Combined with Interventional Photothermal Therapy for the Treatment of Hepatocellular Carcinoma.
Cao, J; Ding, X; Liao, X; Ling, G; Long, Q; Wu, M; Xu, H; Zhou, J; Zhou, X, 2020
)
0.56
"Transcatheter intra-arterial infusion combined with interventional PTT (IPTT) is safe and effective in eradicating tumor cells and inhibiting tumor growth and may provide a novel and valuable choice for the treatment of hepatocellular carcinoma in the future."( Transcatheter Intra-Arterial Infusion Combined with Interventional Photothermal Therapy for the Treatment of Hepatocellular Carcinoma.
Cao, J; Ding, X; Liao, X; Ling, G; Long, Q; Wu, M; Xu, H; Zhou, J; Zhou, X, 2020
)
0.56
"To evaluate the efficacy and economics of different proton pump inhibitors (PPIs) combined with bismuth quadruple regimens for Helicobacter pylori (Hp) eradication, a retrospective analysis method was used to collect Hp-positive patients who were treated with a bismuth-containing quadruple regimen (PPIs + amoxicillin + furazolidone + colloid pectin bismuth) from the outpatient department of gastroenterology in our hospital from January to June 2017."( Evaluation of different proton pump inhibitors combined with bismuth quadruple regimens in Helicobacter pylori eradication.
Chen, J; Chen, Q; Fang, HM; Huang, YT; Kan, LD; Li, LC; Qiu, Y; Yu, XL, 2020
)
0.56
" This study aimed to compare the efficacy of Biling Weitong granules (BLWTG) combined with quadruple therapy in patients with refractory HP infection who had previously failed eradication therapy."( Clinical Effects of Biling Weitong Granules in Combination with Quadruple Therapy on Refractory Helicobacter pylori Infection.
Chen, DL; Chen, YL; Li, ZS; Zhang, HQ, 2023
)
0.91
" And those treated with BLWTG (5 g three times daily) combined with the EACB group for 14 days (BLWTG+EACB group)."( Clinical Effects of Biling Weitong Granules in Combination with Quadruple Therapy on Refractory Helicobacter pylori Infection.
Chen, DL; Chen, YL; Li, ZS; Zhang, HQ, 2023
)
0.91
"To investigate the clinical impact of dietary intervention in combination with bismuth potassium citrate in the management of chronic atrophic gastritis (CAG) caused by Helicobacter pylori."( Clinical Efficacy of Diet Intervention Combined with Bismuth Potassium Citrate in Helicobacter pylori-Related Chronic Atrophic Gastritis.
Ou, S; Xu, Y; Yang, T; Yao, J; Yuan, X; Zuo, X, 2023
)
0.91
"Dietary intervention combined with bismuth potassium citrate exhibited more effective treatment than bismuth potassium citrate-only treatment in Helicobacter pylori-related CAG, which hinted us proper diet has a positive impact on improving the therapeutic efficacy of bismuth potassium citrate."( Clinical Efficacy of Diet Intervention Combined with Bismuth Potassium Citrate in Helicobacter pylori-Related Chronic Atrophic Gastritis.
Ou, S; Xu, Y; Yang, T; Yao, J; Yuan, X; Zuo, X, 2023
)
0.91

Bioavailability

Bioavailability of doxycycline was significantly reduced by 37% and 51%, respectively, when subsalicylate bismuth was given simultaneously and as a multiple-dose regimen. These results suggest that ciprofloxacin bioavailability will not be significantly decreased when the two medications are administered simultaneously.

ExcerptReferenceRelevance
" Apparently, the reduction in tetracycline bioavailability previously reported with a kaolin-pectin suspension is not peculiar to kaolin-pectin but can be expected with almost any antidiarrheal whose mechanism of action is adsorptive in nature."( Decreased tetracycline bioavailability caused by a bismuth subsalicylate antidiarrheal mixture.
Albert, KS; DeSante, KA; DiSanto, AR; Welch, RD, 1979
)
0.26
"The bioavailability of 205Bi from various 205Bi-labelled pharmaceutical oral bismuth preparations was studied in rats."( Bioavailability of bismuth from 205Bi-labelled pharmaceutical oral Bi-preparations in rats.
Dresow, B; Fischer, R; Gabbe, EE; Heinrich, HC; Nielsen, P; Wendel, J, 1991
)
0.28
" Bioavailability of doxycycline was significantly reduced by 37% and 51%, respectively, when subsalicylate bismuth was given simultaneously and as a multiple-dose regimen before doxycycline."( Influence of subsalicylate bismuth on absorption of doxycycline.
Cleary, TG; Ericsson, CD; Feldman, S; Pickering, LK, 1982
)
0.26
" For other otherwise healthy persons, poorly absorbed agents are preferable in order to avoid the serious, albeit rare, toxicity of systemic drugs."( Prevention and treatment of traveler's diarrhea: a clinical pharmacological approach.
Rampal, P; Scarpignato, C, 1995
)
0.29
" These results suggest that ciprofloxacin bioavailability will not be significantly decreased by single doses of bismuth subsalicylate when the two medications are administered simultaneously."( Effect of bismuth subsalicylate on ciprofloxacin bioavailability.
Gallicano, K; Garber, G; Oliveras, L; Rambout, L; Sahai, J, 1994
)
0.29
" First, we examined the impact of the labeling procedure and the presence of the chelate, DOTA, on antibody bioavailability and survival."( Pharmacokinetics and bioactivity of 1,4,7,10-tetra-azacylododecane off',N'',N'''-tetraacetic acid (DOTA)-bismuth-conjugated anti-Tac antibody for alpha-emitter (212Bi) therapy.
Brechbiel, MW; Dobbs, D; Gansow, OA; Junghans, RP; Mirzadeh, S; Raubitschek, AA; Waldmann, TA, 1993
)
0.29
" This, in part, reflects the low systemic bioavailability of bismuth from these medicines: less than 1% of the bismuth dose administered is absorbed."( Review article: safety of bismuth in the treatment of gastrointestinal diseases.
Dixon, JS; Drake, FM; Tillman, LA; Wood, JR, 1996
)
0.29
"To determine whether the observed decrease in tetracycline bioavailability is due to the active drug bismuth subsalicylate via complexation, or to magnesium aluminum silicate (Veegum), an inactive excipient present only in the liquid formulation of bismuth subsalicylate, which might adsorb the tetracycline, rendering it unavailable for systemic absorption."( Reduced tetracycline bioavailability caused by magnesium aluminum silicate in liquid formulations of bismuth subsalicylate.
Clendening, CE; Dansereau, RJ; Deepe, GS; Dunn, AB; Healy, DP; Mounts, AW, 1997
)
0.3
" Hence, the use of effective but poorly absorbed bismuth preparations should be encouraged for bismuth-based eradication therapies."( Double-blind comparison of absorbable colloidal bismuth subcitrate and nonabsorbable bismuth subnitrate in the eradication of Helicobacter pylori and the relief of nonulcer dyspepsia.
Delves, HT; Phillips, RH; Powell, JJ; Seed, PT; Sieniawska, CE; Thompson, RP; Whitehead, MW, 2000
)
0.31
" However, due to the low absorption rate of Bi from the gastrointestinal tract, the efficacy of BSN in inducing renal MT is low."( Citrate enhances the protective effect of orally administered bismuth subnitrate against the nephrotoxicity of cis-diamminedichloroplatinum.
Himeno, S; Imura, N; Kondo, Y; Naganuma, A; Nishimura, T; Satoh, M, 2004
)
0.32
"Food significantly decreased the relative bioavailability of each drug but formulation was without effect."( Effects of food and formulation on the relative bioavailability of bismuth biskalcitrate, metronidazole, and tetracycline given for Helicobacter pylori eradication.
Aumais, C; Brunet, JS; Grace, M; Lefebvre, M; Massicotte, J; Spénard, J; Tremblay, C, 2005
)
0.33
"The bioavailability was measured in 20 healthy male Chinese volunteers following a single oral dose (equivalent to 200 mg of ranitidine and 220 mg of bismuth) of the test or reference products in the fasting state."( Pharmacokinetics and bioequivalence of ranitidine and bismuth derived from two compound preparations.
Jiang, B; Ruan, ZR; Xu, DH; Yuan, H; Zhou, Q, 2006
)
0.33
" With the advent of poorly absorbed (<0."( Current and future developments in travelers' diarrhea therapy.
DuPont, HL; Koo, HL, 2006
)
0.33
" However, bioavailability on these sites needs to be comprehensively characterized."( Integration of toxicological and chemical tools to assess the bioavailability of metals and energetic compounds in contaminated soils.
Auroy, A; Berthelot, Y; Robidoux, PY; Trottier, B; Valton, E, 2008
)
0.35
" However, the bioavailability and toxicity of bismuth is still not very well described."( Multi-elemental bio-imaging of rat tissue from a study investigating the bioavailability of bismuth from shotgun pellets.
Beattie, JH; Berlinger, B; Eilertsen, E; Ellingsen, DG; Feldmann, J; Friisk, G; Kwun, IS; Skaug, V; Thomassen, Y; Urgast, DS, 2012
)
0.38
" Despite their impact on mobility, bioavailability and toxicity of various metal(loid)s, only few papers deal with these processes under aerobic conditions with microscopic fungi."( Bioaccumulation and biovolatilization of various elements using filamentous fungus Scopulariopsis brevicaulis.
Boriová, K; Bujdoš, M; Cerňanský, S; Matúš, P; Simonovičová, A, 2014
)
0.4
" Improving the bioavailability and developing synergistic therapeutic regimens benefit the drug transformation of BNPs."( Platelet-membrane-camouflaged bismuth sulfide nanorods for synergistic radio-photothermal therapy against cancer.
Chen, Y; Du, C; Fan, Z; Han, S; He, Y; Li, S; Wang, C; Wang, J; Wang, S; Zhao, G, 2019
)
0.51

Dosage Studied

The pharmacokinetics of bismuth subcitrate were studied in plasma and urine under conditions of single and multiple dosing (28-56 days) using atomic absorption technique. Twelve healthy male subjects were dosed with six regimens: ranitidine and De-Noltab. Twenty four men with duodenal ulcers were studied before and on the 8th day of dosing.

ExcerptRelevanceReference
"Six-mercaptopurine and its Pt, Pd and Bi complexes were used at various dosage levels to treat Dunning ascitic leukemia in rats."( Anti leukemia activity (Dunning ascitic) of 6-mercaptopurine and its metallo complexes in rats.
Lewis, RW; Skinner, SM; Swatzell, JM, 1978
)
0.26
"Six-mercaptopurine in the free form and complexed with Pt, Pd, or Bi metals was used at various dosage levels to treat L1210 leukemia in mice."( Anti leukemia activity (L1210) of 6-mercaptopurine and its metallo complexes in mice.
Lewis, RW; Skinner, SM, 1977
)
0.26
" Recombinant human (rHu) EPO (5000 units) in a dosing solution or in a rectal suppository was placed in the rectum of healthy rats and changes in serum EPO levels were monitored by an enzyme-linked immunosorbent assay."( Effects of salicylate and other enhancers on rectal absorption of erythropoietin in rats.
Kawanishi, G; Mizuno, A; Ueda, M, 1992
)
0.28
" Substitution of doxycycline for tetracycline HCl offers advantages of less frequent dosing and extrarenal excretion."( Helicobacter pylori eradication with doxycycline-metronidazole-bismuth subcitrate triple therapy.
Andrews, P; Borody, TJ; Brandl, S; Devine, M; George, LL; Lenne, J; Moore-Jones, D; Walton, M, 1992
)
0.28
"Electron microscopic examination of upper gastrointestinal biopsies with x-ray microanalysis was used to detect electron-dense particles of bismuth in the mucosa of the upper gastrointestinal tract, 30-60 minutes after oral dosing with either tripotassium dicitrato bismuthate [De-Noltab; Brocades (Great Britain) Ltd."( Transmucosal penetration of bismuth particles in the human stomach.
Hudson, M; Lewin, JF; Nwokolo, CU; Pounder, RE, 1992
)
0.28
" Side effects so far reported have been very infrequent mild and transient when the drug is used at low dosage providing blood-bismuth concentration above toxic values."( [Bismuth revisited in Helicobacter pylori gastro-duodenal infection].
Caron, F; Rouveix, B,
)
0.13
" It appears prudent to halve tripotassium dicitrato bismuthate dosage in patients with severe renal insufficiency (creatinine clearance less than or equal to 20 ml/min) to avoid any possible toxic risks."( Tripotassium dicitrato bismuthate: absorption and urinary excretion of bismuth in patients with normal and impaired renal function.
Gladziwa, U; Ittel, TH; Klotz, U; Schweinsberg, F; Treiber, G; Walker, S, 1991
)
0.28
"Twelve healthy male subjects were dosed with six regimens: ranitidine and De-Noltab (tripotassium dicitrato bismuthate; Gist-Brocades Ltd."( The effect of histamine H2-receptor blockade on bismuth absorption from three ulcer-healing compounds.
Hudson, M; Nwokolo, CU; Pounder, RE; Prewett, EJ; Sawyerr, AM, 1991
)
0.28
" The dosing regimen was 20 mg/kg five times daily for 5 days."( Bismuth subsalicylate in the treatment of acute diarrhea in children: a clinical study.
Avendaño, P; Balm, TK; Braun, SD; Manhart, MD; O'Ryan, M; Soriano, HA; Soriano-Brücher, H, 1991
)
0.28
" In spite of the high dosage as well as the large interindividual variability in the urinary recovery and the serum concentrations potential "toxic" serum levels of 100 micrograms/l were never reached."( [Effect of meals on resorption of bismuth from an oral bismuth gallate/bismuth nitrate preparation].
Klotz, U; Leonhardt, H, 1991
)
0.28
" It proved possible to reduce the oral prednisolone dosage from a median of 15 mg/day (range 10 to 35 mg/day) to 6 mg/day (range 0 to 18 mg/day) after 8 weeks of treatment; 5 patients were no longer taking oral steroids at this time."( Rectal bismuth subsalicylate as therapy for ulcerative colitis.
Jones, H; Rhodes, JM; Ryder, SD; Walker, RJ, 1990
)
0.28
"2% of the ingested dose) and sequestration of this heavy metal in multiple tissue sites, even occurring with conventional dosing over a 6-week period."( Bismuth therapy in gastrointestinal diseases.
Gorbach, SL, 1990
)
0.28
" Before dosing with D-penicillamine, the median 24 h urinary bismuth output was 55 micrograms 24 h-1 (range 17-156 micrograms 24 h-1) and following dosing with D-penicillamine the median 24 h urinary bismuth output was 53 micrograms 24 h-1 (range 12-156 micrograms 24 h-1)."( D-penicillamine does not increase urinary bismuth excretion in patients treated with tripotassium dicitrato bismuthate.
Nwokolo, CU; Pounder, RE, 1990
)
0.28
" Of three dosage regimens tested, continuous treatment before and after the bacterial challenge, mimicking the way BSS is used in the prevention of traveller's diarrhoea, was the most effective."( Bismuth subsalicylate in the prevention of colonization of infant mice with Campylobacter jejuni.
Hänninen, ML, 1990
)
0.28
" Extended dosing of Pepto-Bismol (3."( Bismuth subsalicylate: history, chemistry, and safety.
Bierer, DW,
)
0.13
" Patients received either BSS at a dosage of 100 mg/(kg."( Use of bismuth subsalicylate in acute diarrhea in children.
Avendaño, P; O'Ryan, M; Soriano, HA; Soriano-Brücher, HE,
)
0.13
" In the first study, 62 subjects received BSS for 3 weeks at a dosage of 60 mL four times daily (4."( Use of bismuth subsalicylate for the prevention of travelers' diarrhea.
de la Cabada, FJ; DuPont, HL; Ericsson, CD; Johnson, PC,
)
0.13
" Such risk assessment should be based upon careful evaluation of scientific findings of dose-response relationships in the chronically exposed population."( Health assessment of environmental pollutants: proliferative and degenerative diseases.
Stuart, BO, 1988
)
0.27
"Two studies measured plasma concentrations of bismuth during dosing with tripotassium dicitrato bismuthate (De-Noltab)."( The absorption of bismuth from oral doses of tripotassium dicitrato bismuthate.
Gavey, CJ; Nwokolo, CU; Pounder, RE; Smith, JT, 1989
)
0.28
"The pharmacokinetics of bismuth subcitrate were studied in plasma and urine under conditions of single and multiple dosing (28-56 days) using atomic absorption technique."( Absorption and elimination of bismuth from oral doses of tripotassium dicitrato bismuthate.
Froomes, PR; Keech, AC; McLean, AJ; McNeil, JJ; Wan, AT, 1989
)
0.28
" Slopes of dose-response relations for lung cancer show a tendency to decrease with increasing dose."( Estimates of lifetime lung cancer risks resulting from Rn progeny exposure.
Dougherty, C; McNeill, KG; Thomas, DC, 1985
)
0.27
" However, no such intoxication has been reported with CBS used at its recommended dosage in the acute treatment of peptic ulcer disease, and no other serious adverse effects have been associated with CBS."( Colloidal bismuth subcitrate. A review of its pharmacodynamic and pharmacokinetic properties, and its therapeutic use in peptic ulcer disease.
Benfield, P; Monk, JP; Wagstaff, AJ, 1988
)
0.27
" Because it has been suggested that the lower relapse rate for duodenal ulcer following colloidal bismuth subcitrate (CBS) is due to suppression of C pylori we investigated different formulations and dosing of CBS for their efficacy in clearing C pylori."( Treatment of Campylobacter pylori gastritis: a pilot study using pirenzepine dihydrochloride (Gastrozepin) and three formulations of colloidal bismuth subcitrate (De-Nol).
Ali, MR; Brown, P; Lane, M; Morris, A; Palmer, R, 1988
)
0.27
"025), bismuth subsalicylate (Pepto-Bismol) taken orally at a dosage of as low as 30 ml every half hour for eight doses was shown to be effective in reducing the frequently of episodes of diarrhea."( Nonantibiotic therapy for travelers' diarrhea.
DuPont, HL; Ericsson, CD; Johnson, PC,
)
0.13
"Forty patients with endoscopically proven duodenal ulceration have cooperated in a clinical trial to compare the ulcer healing effect of colloidal bismuth subcitrate (CBS) at standard dosage administered either twice or four times a day."( Colloidal bismuth subcitrate as coated tablets: four times versus twice daily dosage in duodenal ulcer.
Bianchi Porro, G; Lazzaroni, M; Parente, F; Prada, A, 1986
)
0.27
"Fifty three patients with endoscopically proven duodenal ulceration have cooperated in a clinical trial to compare the ulcer healing effect of tripotassium dicitrato bismuthate (TDB) at standard dosage administered either twice or four times daily."( Twice daily tripotassium dicitrato bismuthate in the treatment of duodenal ulceration.
Hollanders, D, 1986
)
0.27
" In dose-response experiments, B16F10 mouse melanoma cells were incubated with liposomes 212Pb/212Bi bound to dextran 70."( In vitro killing of melanoma by liposome-delivered intracellular irradiation.
Parks, NJ; Pikul, SS; Schneider, PD, 1987
)
0.27
" The dosage of two tablets of bismuth subsalicylate four times daily (2."( Prevention of travelers' diarrhea by the tablet formulation of bismuth subsalicylate.
Bitsura, JA; de la Cabada, FJ; DuPont, HL; DuPont, MW; Ericsson, CD; Johnson, PC, 1987
)
0.27
" Treatment was given for 7 days with dosage varied according to age."( Bismuth subsalicylate in the treatment of chronic diarrhea of childhood.
Grill, B; Gryboski, JD; Hillemeier, AC; Kocoshis, S, 1985
)
0.27
" Most of the commercially available and investigational compounds have similar efficacy; therefore the optimal drug may be the one associated with the fewest adverse effects and the most convenient dosing regimen."( Problems associated with medical treatment of peptic ulcer disease.
Zimmerman, TW, 1984
)
0.27
"The efficacy of a daily dosage regimen of subsalicylate bismuth in preventing or reducing the severity of diarrhea among young healthy adults was evaluated in a double-blind, randomized, placebo-controlled trial."( Prevention of traveler's diarrhea (emporiatric enteritis). Prophylactic administration of subsalicylate bismuth).
Ackerman, PB; DuPont, HL; Ericsson, CD; Evans, DG; Evans, DJ; Pickering, LK; Sullivan, P; Tjoa, WS; Vollet, JJ, 1980
)
0.26
" After ulcer healing, drug dosage was reduced (cimetidine to 400 mg at night and Caved-S to two tablets twice daily)."( Comparison between cimetidine and Caved-S in the treatment of gastric ulceration, and subsequent maintenance therapy.
Darnborough, A; McAdam, WA; Morgan, AG; Pacsoo, C, 1982
)
0.26
"Impulsion polarography with anodic redissolution, a very sensitive means of dosage that is easy to repeat and more selective than atomic absorption, makes it possible to affirm the presence of bismuth in the bones after oral or parenteral treatment in 6 patients, 5 of whom suffered from osteoarthropathies that could be linked, given their nature, to the treatment administered, though this could not be proven."( [Bismuth osteoarthropathies. Concern with bone bismuth dosage].
Burnel, D; Faure, G; Gaucher, A; Hutin, MF; Netter, P; Pourel, J, 1980
)
0.26
" At day 70 of dosing the mean plasma bismuth concentration was 63."( Plasma and tissue distribution of bismuth in normal and cirrhotic rats.
Luppino, MA; McLean, AJ, 1995
)
0.29
"-azithromycin dosage regime (83%) (95% CI = 52-98%) compared to the 250-mg-b."( Azithromycin triple therapy for Helicobacter pylori infection: azithromycin, tetracycline, and bismuth.
al-Assi, MT; Cole, RA; Genta, RM; Graham, DY; Karttunen, TJ, 1995
)
0.29
" Thirty minutes after dosing each subject was given 375 ml of 99mTc-DTPA (diethylene triaminepentaacetic acid) labelled Clinifeed-ISO."( Ranitidine bismuth citrate and ranitidine do not affect gastric emptying of a radio-labelled liquid meal.
Bedding, AW; Farr, SJ; Forster, ER; Parikh, R; Smith, JT; Sweetland, J, 1994
)
0.29
" The median integrated 6-hour serum bismuth concentration after dosing with CBS and BSG was 49 and 32 ng h/ml, respectively, after dosing with BSC, BA, BSS, BSN and BSN1480 13, 11, 3, 0 and 5 ng h/ml, respectively."( [Absorption and renal elimination of bismuth from 6 different bismuth salts after a single dosage].
Bödeker, RH; Heckers, H; Mannl, MR; Muskat, E; Stelz, A, 1994
)
0.29
" For successful triple therapy with complicated dosage protocols cooperation with and compliance by the patient is stressed."( [Clinico-pharmacologic considerations in Helicobacter pylori eradication therapy].
Leiss, O; Von Bergmann, K,
)
0.13
" The maximum percentages of cells accumulated in G2M 18 h after alpha- and gamma-irradiation were comparable, though the dose-response relationships differed."( G2M arrest and apoptosis in murine T lymphoma cells following exposure to 212Bi alpha particle irradiation.
Atcher, RW; Hines, JJ; Humm, JL; Macklis, RM; Palayoor, ST, 1993
)
0.29
" Twenty four men with duodenal ulcers were studied before and on the 8th day of dosing with either ranitidine bismuth citrate 800 mg twice daily or ranitidine 300 mg twice daily (double blind, randomised, parallel groups)."( Effect of ranitidine bismuth citrate on postprandial plasma gastrin and pepsinogens.
Fraser, AG; Hudson, M; Lam, WM; Luk, YW; Pounder, RE; Samloff, IM; Sawyerr, AM; Sercombe, J, 1993
)
0.29
" However, the energy deposition pattern will be strongly dependent upon the configuration of alpha-particle sources relative to the cells, and will consequently impact upon the dose-response characteristics."( A model of cell inactivation by alpha-particle internal emitters.
Chin, LM; Humm, JL, 1993
)
0.29
"To determine whether bismuth penetrates the gastric mucosa after dosing with ranitidine bismuth citrate."( Gastric persorption of bismuth from ranitidine bismuth citrate.
Fraser, AG; Lewin, JF; Pounder, RE, 1995
)
0.29
"Bismuth particles were found to be interposed between epithelial cells in the antral mucosa of three of eight patients who were dosed with ranitidine bismuth citrate."( Gastric persorption of bismuth from ranitidine bismuth citrate.
Fraser, AG; Lewin, JF; Pounder, RE, 1995
)
0.29
"Penetration of bismuth particles into the gastric mucosa may occur after oral dosing with ranitidine bismuth citrate."( Gastric persorption of bismuth from ranitidine bismuth citrate.
Fraser, AG; Lewin, JF; Pounder, RE, 1995
)
0.29
"This review provides an updated overview on Helicobacter pylori (HP) trials, focusing on drug dosage and cost:benefit ratio."( The influence of drug dosage on Helicobacter pylori eradication: a cost-effectiveness analysis.
Treiber, G, 1996
)
0.29
" In addition, the incidence of micronucleus induction seemed to be reduced by double dosing with K2CrO4 and H2SeO3, compared to single dosing."( Micronucleus induction by chromium and selenium, and suppression by metallothionein inducer.
Itoh, S; Shimada, H, 1996
)
0.29
" These drawbacks have thus stimulated research aimed at identifying better drug combinations, with a simpler dosage for a shorter period, fewer side-effects, and greater and more consistent efficacy."( Eradication of Helicobacter pylori: omeprazole in combination with antibiotics.
Axon, AT; Moayyedi, P, 1996
)
0.29
"Bismuth (Bi) can produce neurotoxic effects in both humans and animals under certain dosing conditions, but little else is known about the effects of Bi in the brain."( Distribution of bismuth in the brain after intraperitoneal dosing of bismuth subnitrate in mice: implications for routes of entry of xenobiotic metals into the brain.
Lawhorn, GT; Poston, MR; Ross, JF; Switzer, RC, 1996
)
0.29
" pylori eradication is effected, the optimal dosing schedules, and the specific antimicrobial agents to be administered require further study, the combination of a proton pump inhibitor and one or two antibiotics promises to be an appropriate first-line treatment for peptic ulcer disease."( Peptic ulcer disease: defining the treatment strategies in the era of Helicobacter pylori.
Hunt, RH, 1997
)
0.3
" Although the dosage of omeprazole in pediatric patients has not been established (no pediatric formulation exists), clarithromycin is available for use in pediatric patients."( Guidelines for the treatment of Helicobacter pylori in the pediatric population.
Abdel-Rahman, SM; Nahata, MC; Robinson, DM, 1997
)
0.3
"Disposition pharmacokinetics of bismuth following oral dosing of ranitidine bismuth citrate are complicated and variable."( Modeling of trough plasma bismuth concentrations.
Bennett, JE; Lacey, LF; Wakefield, JC, 1997
)
0.3
" Such a synergistic effect probably explains the increased efficacy of RBC-clarithromycin dual therapies compared with clarithromycin dosed with acid-suppressive agents such as H2-receptor antagonists or proton-pump inhibitors."( New options in Helicobacter pylori eradication: efficacy, resistance and synergy.
Pipkin, GA; Williamson, R; Wood, JR, 1998
)
0.3
" After dosing with bismuth alone or in association with ranitidine hydrochloride, bismuth was detected in several organs and deposition was not influenced by gastric pH."( Distribution of bismuth in the rat after oral dosing with ranitidine bismuth citrate and bismuth subcitrate.
Canena, J; Leitão, J; Pinheiro, T; Pinto, AS; Quina, MG; Reis, J; Santos, AM, 1998
)
0.3
"Helicobacter pylori eradication is accomplished using a wide array of drugs combined in a multitude of dosage schedules."( Optimal PPI-based triple therapy for the cure of Helicobacter pylori infection: a single center comparison of four 14-day schedules.
Battaglia, G; Benvenuti, ME; Del Bò, N; Di Mario, F; Donisi, PM; Leandro, G; Pasini, M; Pasquino, M; Vianello, F; Vigneri, S, 1998
)
0.3
" dosing schedule: RBC 400 mg plus clarithromycin 250 mg and tinidazole 500 mg (RBCCT): RBC 400 mg plus clarithromycin 500 mg and amoxycillin 1 g (RBCCA); RBC 400 mg plus tinidazole 500 mg and amoxycillin 1 g (RBCTA)."( Efficacy and safety of three 7-day Helicobacter pylori eradication regimens containing ranitidine bismuth citrate.
Bazzoli, F; Cannizzaro, O; D'Angelo, A; Ederle, A; Fossi, S; Gerace, G; Iaquinto, G; Olivieri, A; Pozzato, P; Reina, G; Ricciardiello, L; Roda, E; Scarpulla, G; Spadaccini, A; Tosatto, R; Zagari, M, 1998
)
0.3
" Bacterial infections were absent in all dosed ducks."( Effects of lead, iron, and bismuth alloy shot embedded in the breast muscles of game-farm mallards.
Anderson, WL; Brawn, JW; Foley, GL; Havera, SP; Sanderson, GC; Seets, JW; Skowron, LM; Taylor, GD, 1998
)
0.3
"In order to improve the efficacy and simplicity of the FDA-approved regimen of ranitidine bismuth citrate (RBC) and clarithromycin dual therapy, we added an inexpensive antibiotic (metronidazole), changed the dosage scheme to twice daily dosing, and decreased the duration of therapy to 1 week."( Efficacy of a 1-week regimen of ranitidine bismuth citrate in combination with metronidazole and clarithromycin for Helicobacter pylori eradication.
Cave, DR; Hoffman, JS; Katz, LM, 1999
)
0.3
" Pre-treatment with a proton pump inhibitor, higher doses or more frequent dosing may be necessary to increase the cure rate of short duration regimens."( Comparison of two 3-day Helicobacter pylori eradication regimens with a standard 1-week regimen.
Cross, R; Grimley, CE; Illing, RC; Lismore, JR; Loft, DE; Nwokolo, CU; O'sullivan, M; Penny, A; Shebani, M, 1999
)
0.3
" Other factors reported to affect compliance included the frequency of dosing and the number of pills."( A randomized controlled trial of an enhanced patient compliance program for Helicobacter pylori therapy.
Canning, A; Egan, C; Farraye, FA; Kemp, JA; Lee, M; Tataronis, G, 1999
)
0.3
" pylori eradication rate with a standard triple therapy regardless of the regimen utilized, the dosage and/or the duration of the therapy used appearing not to be sufficient to eradicate the infection efficiently."( Efficacy of different Helicobacter pylori eradication regimens in patients affected by insulin-dependent diabetes mellitus.
Armuzzi, A; Gasbarrini, A; Gasbarrini, G; Ghirlanda, G; Ojetti, V; Pitocco, D; Pola, P; Silveri, NG, 2000
)
0.31
"The phantom study demonstrated that the use of bismuth-coated shielding over the eyes decreased radiation dosage by 48."( Radioprotection to the eye during CT scanning.
Hopper, KD; King, SH; Kunselman, AR; Neuman, JD,
)
0.13
" Thirty-two bird groups (sexes equal) of adult mallards were dosed orally with eight #4 steel shot (control), eight #4 tungsten-iron shot, or eight #4 tungsten-polymer shot on days 0, 30, 60, 90, and 120 of a 150-day trial (26 January 1998 to 25 June 1998)."( Health effects following chronic dosing with tungsten-iron and tungsten-polymer shot in adult game-farm mallards.
Aulerich, RJ; Balander, RJ; Bursian, SJ; Fitzgerald, SD; Mitchell, RR; Powell, DC; Stevens, W; Stickle, RL; Tempelman, RJ, 2001
)
0.31
"We evaluated the effect of optimized doses and dosing schedules of metronidazole, tetracycline, and bismuth-metronidazole-tetracycline (BMT) triple therapy with only 1 day of dosing on Helicobacter pylori SS1 titers in a mouse model."( Effects of metronidazole, tetracycline, and bismuth-metronidazole-tetracycline triple therapy in the Helicobacter pylori SS1 mouse model after 1 day of dosing: development of an H. pylori lead selection model.
Amsler, KM; Foster, LA; Merrill, JJ; Modzelewski, TC; Quispe, JD; Sizemore, CF; Slee, AM; Stevenson, DA, 2002
)
0.31
" According to the dosage regimen the patients were divided into two groups."( [Effectiveness of eradication anti-helicobacter therapy in patients with duodenal ulcer in different drug dosage regimens].
Nurbaev, FE; Orziev, ZM; Rakhimova, GSh, 2003
)
0.32
" When cases treated with "adequate" dosage of arsenic and bismuth are analysed by the same statistical method as that employed in evaluating penicillin, the superiority of penicillin is clearly evident."( Long-term studies of results of penicillin therapy in early syphilis.
PRICE, EV; SHAFER, JK; USILTON, LJ, 1954
)
0.23
" Since the cellular consumption of metals in the transferrin cycle critically depends upon recognition of the holo-protein complex by the transferrin receptor, the noncanonical conformation of the transferrin-bismuth complex may explain very inefficient delivery of bismuth to cells even when a high dosage of bismuth-containing drugs is administered for prolonged periods of time."( Indirect detection of protein-metal binding: interaction of serum transferrin with In3+ and Bi3+.
Gumerov, DR; Kaltashov, IA; Mason, AB; Zhang, M, 2004
)
0.32
" dosing of levofloxacin (81%[95% CI: 78%-89%]vs 84%[95% CI: 66%-97%])."( Levofloxacin-based triple therapy versus bismuth-based quadruple therapy for persistent Helicobacter pylori infection: a meta-analysis.
Chey, WD; Kim, HM; Saad, RJ; Schoenfeld, P, 2006
)
0.33
" The negative control and the (213)Bi-CD19 groups were combined to investigate the dose-response relationship for model parameters describing the formation and growth of foci of altered hepatocytes."( Investigating the formation and growth of alpha-particle radiation-induced foci of altered hepatocytes: a model-based approach.
Bannasch, P; Burkholder, I; Groos, J; Haertel, T; Heeger, S; Kopp-Schneider, A; Wesch, H, 2006
)
0.33
" For the 50 ppm treatment group, only birds dosed with bismuth citrate for 21 d demonstrated any reduction in cecal Campylobacter concentrations when compared with controls."( Effect of oral administration of bismuth compounds on Campylobacter colonization in broilers.
Blore, PJ; Cole, K; de Los Santos, FS; Dirain, ML; Donoghue, AM; Donoghue, DJ; Farnell, MB; Pandya, K; Reyes-Herrera, I, 2006
)
0.33
" pylori treatment: effectiveness (>80%), simplicity (twice-daily dosing and excellent compliance) and safety (low incidence of adverse effects)."( First-line triple therapy with levofloxacin for Helicobacter pylori eradication.
Fernández-Bermejo, M; Gisbert, JP; González-García, G; Mateos-Rodríguez, JM; Molina-Infante, J; Pérez-Gallardo, B; Prieto-Bermejo, AB; Robledo-Andrés, P, 2007
)
0.34
" Although dosing regimens of clarithromycin triple therapy were quite consistent between trials, dosing regimens varied considerably for bismuth quadruple therapy."( Empiric quadruple vs. triple therapy for primary treatment of Helicobacter pylori infection: Systematic review and meta-analysis of efficacy and tolerability.
Chey, WD; Higgins, PD; Luther, J; Moayyedi, P; Schoenfeld, PS; Vakil, N, 2010
)
0.36
" The oral dosing regimen selected for subsequent phase II/III clinical trials was 800 mg twice daily."( Safety and tolerability of bismuthyl ecabet suspension, a novel anti-ulcer agent, following single and multiple oral dose administration in healthy Chinese subjects.
Chen, A; Jiang, N; Meng, L; Ou, N; Shi, R; Tang, N; Wang, Y; Wu, D; Xu, K; Zhang, H; Zhang, P; Zhang, X, 2012
)
0.38
"9)O(8)I was as high as 92% within 12 h visible light irradiation under the optimal conditions: initial MO concentration of 5-10 mg L(-1), catalyst dosage of 6 g L(-1) and natural pH (6-8), the MO molecules could be completely degradated by Bi(4)Nb(0."( Photocatalytic removal of organic pollutants in aqueous solution by Bi(4)Nb(x)Ta((1-x))O(8)I.
Fan, J; Hu, XY; Wang, JJ; Zhang, KL, 2012
)
0.38
" Possibly, it can be improved by alterations in dose, dosing intervals, and/or duration."( A modified bismuth-containing quadruple therapy including a short course of furazolidone for Helicobacter pylori eradication after sequential therapy failure.
Bari, Z; Fakheri, H; Sardarian, H, 2012
)
0.38
", nearly 100%, was observed with the BiOI/BiOCl composite (containing 90% BiOI) using a catalyst dosage of 1 g L(-1) in the BPA solution (C(0)=20 mg L(-1), pH=7."( One-pot solvothermal synthesis of three-dimensional (3D) BiOI/BiOCl composites with enhanced visible-light photocatalytic activities for the degradation of bisphenol-A.
Hao, R; Li, L; Liang, M; Nan, J; Xiao, X; Zhang, W; Zuo, X, 2012
)
0.38
" It might be related to the low dosage of our probiotic regimen and/or high frequency of upper gastrointestinal adverse effects which in turn could decrease the eradication efficacy."( The effects of multistrain probiotic compound on bismuth-containing quadruple therapy for Helicobacter pylori infection: a randomized placebo-controlled triple-blind study.
Gholamrezaei, A; Hashemi, H; Khodadoostan, M; Minakari, M; Shavakhi, A; Shavakhi, S; Tabesh, E; Tabesh, F; Yaghoutkar, A, 2013
)
0.39
"Pediatricians in Africa requested a tool to improve caregiver dosing of liquid antiretroviral medication."( Design, evaluation, and dissemination of a plastic syringe clip to improve dosing accuracy of liquid medications.
Adler, M; Dinh, C; Gray, LV; Gutierrez, A; Lu, B; Lukomnik, J; Marton, S; Mirabal, Y; Oden, M; Richards-Kortum, R; Schutze, GE; Shah, K; Slough, T; Spiegel, GJ; Wickham, H; Yeh, PT, 2013
)
0.39
", doses, dosing interval, dosing in relation to meals, formulation, etc."( Bismuth-containing quadruple therapy for Helicobacter pylori: lessons from China.
Graham, DY; Lu, H; Zhang, W, 2013
)
0.39
" The observed reaction rate constant (kobs) was related to nanoparticles dosage and initial solution pH."( Synthesis of BiOI-TiO2 composite nanoparticles by microemulsion method and study on their photocatalytic activities.
Chen, Y; Chu, J; Fang, J; Liu, Z; Wu, S; Xu, W; Xu, X; Zhou, G; Zhu, X, 2014
)
0.4
" The first step of the study was to assess the dose-response of Melphalan 21 days after engraftment."( Comparative analysis of multiple myeloma treatment by CD138 antigen targeting with bismuth-213 and Melphalan chemotherapy.
Bruchertseifer, F; Chérel, M; Davodeau, F; Faivre-Chauvet, A; Gaschet, J; Gouard, S; Kraeber-Bodéré, F; Matous, E; Maurel, C; Morgenstern, A; Pallardy, A, 2014
)
0.4
" Effects of the molar ratio of Ag/Bi during BSO preparation and the BSO dosage on the degradation of TBBPA were investigated."( [Efficient oxidative degradation of tetrabromobisphenol A by silver bismuth oxide].
Chen, MT; Ding, YB; Liao, HX; Song, Z; Wang, N; Zhu, LH, 2015
)
0.42
" At a low dosage of 10 μg mL(-1), HeLa cells could be efficiently killed through a synergistic effect of chemo- and photothermo-therapy respectively based on the DOX release and the photothermal effect of Cu3BiS3 HNSs."( PEGylated Cu3BiS3 hollow nanospheres as a new photothermal agent for 980 nm-laser-driven photothermochemotherapy and a contrast agent for X-ray computed tomography imaging.
Chen, W; Huang, SM; Ma, DK; Wang, W; Yu, K; Zhang, SH; Zhou, SM, 2016
)
0.43
" This method has been applied in the determination of isoproterenol in dosage forms and in biological fluids."( Selective separation and determination of isoproterenol on thin layers of bismuth silicate ion-exchanger.
, 2015
)
0.42
" DMF was dosed twice-daily (BID) at 120 mg (week 1) and 240 mg (weeks 2-8)."( Effect of Bismuth Subsalicylate on Gastrointestinal Tolerability in Healthy Volunteers Receiving Oral Delayed-release Dimethyl Fumarate: PREVENT, a Randomized, Multicenter, Double-blind, Placebo-controlled Study.
Chalkias, S; Edwards, MR; Koulinska, I; Riester, K, 2018
)
0.48
" In contrast, patients in the SMRE group received extra short messages including dosage and time of administration twice daily."( Twice daily short-message-based re-education could improve Helicobacter pylori eradication rate in young population: A prospective randomized controlled study.
Ji, C; Li, L; Li, Y; Liu, J; Sun, Y; Wang, T; Yang, X; Zuo, X, 2019
)
0.51
" The efficacy of MMF as an immunosuppressant and long-term safety in cats of this dosage regimen is unknown."(
Abrams, G; Adolfsson, E; Agarwal, PK; Akkan, AG; Al Alhareth, NS; Alves, VGL; Armentano, R; Bahroos, E; Baig, M; Baldridge, KK; Barman, S; Bartolucci, C; Basit, A; Bertoli, SV; Bian, L; Bigatti, G; Bobenko, AI; Boix, PP; Bokulic, T; Bolink, HJ; Borowiec, J; Bulski, W; Burciaga, J; Butt, NS; Cai, AL; Campos, AM; Cao, G; Cao, Y; Čapo, I; Caruso, ML; Chao, CT; Cheatum, CM; Chelminski, K; Chen, AJW; Chen, C; Chen, CH; Chen, D; Chen, G; Chen, H; Chen, LH; Chen, R; Chen, RX; Chen, X; Cherdtrakulkiat, R; Chirvony, VS; Cho, JG; Chu, K; Ciurlino, D; Coletta, S; Contaldo, G; Crispi, F; Cui, JF; D'Esposito, M; de Biase, S; Demir, B; Deng, W; Deng, Z; Di Pinto, F; Domenech-Ximenos, B; Dong, G; Drácz, L; Du, XJ; Duan, LJ; Duan, Y; Ekendahl, D; Fan, W; Fang, L; Feng, C; Followill, DS; Foreman, SC; Fortunato, G; Frew, R; Fu, M; Gaál, V; Ganzevoort, W; Gao, DM; Gao, X; Gao, ZW; Garcia-Alvarez, A; Garza, MS; Gauthier, L; Gazzaz, ZJ; Ge, RS; Geng, Y; Genovesi, S; Geoffroy, V; Georg, D; Gigli, GL; Gong, J; Gong, Q; Groeneveld, J; Guerra, V; Guo, Q; Guo, X; Güttinger, R; Guyo, U; Haldar, J; Han, DS; Han, S; Hao, W; Hayman, A; He, D; Heidari, A; Heller, S; Ho, CT; Ho, SL; Hong, SN; Hou, YJ; Hu, D; Hu, X; Hu, ZY; Huang, JW; Huang, KC; Huang, Q; Huang, T; Hwang, JK; Izewska, J; Jablonski, CL; Jameel, T; Jeong, HK; Ji, J; Jia, Z; Jiang, W; Jiang, Y; Kalumpha, M; Kang, JH; Kazantsev, P; Kazemier, BM; Kebede, B; Khan, SA; Kiss, J; Kohen, A; Kolbenheyer, E; Konai, MM; Koniarova, I; Kornblith, E; Krawetz, RJ; Kreouzis, T; Kry, SF; Laepple, T; Lalošević, D; Lan, Y; Lawung, R; Lechner, W; Lee, KH; Lee, YH; Leonard, C; Li, C; Li, CF; Li, CM; Li, F; Li, J; Li, L; Li, S; Li, X; Li, Y; Li, YB; Li, Z; Liang, C; Lin, J; Lin, XH; Ling, M; Link, TM; Liu, HH; Liu, J; Liu, M; Liu, W; Liu, YP; Lou, H; Lu, G; Lu, M; Lun, SM; Ma, Z; Mackensen, A; Majumdar, S; Martineau, C; Martínez-Pastor, JP; McQuaid, JR; Mehrabian, H; Meng, Y; Miao, T; Miljković, D; Mo, J; Mohamed, HSH; Mohtadi, M; Mol, BWJ; Moosavi, L; Mosdósi, B; Nabu, S; Nava, E; Ni, L; Novakovic-Agopian, T; Nyamunda, BC; Nyul, Z; Önal, B; Özen, D; Özyazgan, S; Pajkrt, E; Palazon, F; Park, HW; Patai, Á; Patai, ÁV; Patzke, GR; Payette, G; Pedoia, V; Peelen, MJCS; Pellitteri, G; Peng, J; Perea, RJ; Pérez-Del-Rey, D; Popović, DJ; Popović, JK; Popović, KJ; Posecion, L; Povall, J; Prachayasittikul, S; Prachayasittikul, V; Prat-González, S; Qi, B; Qu, B; Rakshit, S; Ravelli, ACJ; Ren, ZG; Rivera, SM; Salo, P; Samaddar, S; Samper, JLA; Samy El Gendy, NM; Schmitt, N; Sekerbayev, KS; Sepúlveda-Martínez, Á; Sessolo, M; Severi, S; Sha, Y; Shen, FF; Shen, X; Shen, Y; Singh, P; Sinthupoom, N; Siri, S; Sitges, M; Slovak, JE; Solymosi, N; Song, H; Song, J; Song, M; Spingler, B; Stewart, I; Su, BL; Su, JF; Suming, L; Sun, JX; Tantimavanich, S; Tashkandi, JM; Taurbayev, TI; Tedgren, AC; Tenhunen, M; Thwaites, DI; Tibrewala, R; Tomsejm, M; Triana, CA; Vakira, FM; Valdez, M; Valente, M; Valentini, AM; Van de Winckel, A; van der Lee, R; Varga, F; Varga, M; Villarino, NF; Villemur, R; Vinatha, SP; Vincenti, A; Voskamp, BJ; Wang, B; Wang, C; Wang, H; Wang, HT; Wang, J; Wang, M; Wang, N; Wang, NC; Wang, Q; Wang, S; Wang, X; Wang, Y; Wang, Z; Wen, N; Wesolowska, P; Willis, M; Wu, C; Wu, D; Wu, L; Wu, X; Wu, Z; Xia, JM; Xia, X; Xia, Y; Xiao, J; Xiao, Y; Xie, CL; Xie, LM; Xie, S; Xing, Z; Xu, C; Xu, J; Yan, D; Yan, K; Yang, S; Yang, X; Yang, XW; Ye, M; Yin, Z; Yoon, N; Yoon, Y; Yu, H; Yu, K; Yu, ZY; Zhang, B; Zhang, GY; Zhang, H; Zhang, J; Zhang, M; Zhang, Q; Zhang, S; Zhang, W; Zhang, X; Zhang, Y; Zhang, YW; Zhang, Z; Zhao, D; Zhao, F; Zhao, P; Zhao, W; Zhao, Z; Zheng, C; Zhi, D; Zhou, C; Zhou, FY; Zhu, D; Zhu, J; Zhu, Q; Zinyama, NP; Zou, M; Zou, Z, 2019
)
0.51
"Findings will provide timely information on the safety, efficacy, and optimal dosing of t-PA to treat moderate/severe COVID-19-induced ARDS, which can be rapidly adapted to a phase III trial (NCT04357730; FDA IND 149634)."(
Abbasi, S; Abd El-Wahab, A; Abdallah, M; Abebe, G; Aca-Aca, G; Adama, S; Adefegha, SA; Adidigue-Ndiome, R; Adiseshaiah, P; Adrario, E; Aghajanian, C; Agnese, W; Ahmad, A; Ahmad, I; Ahmed, MFE; Akcay, OF; Akinmoladun, AC; Akutagawa, T; Alakavuklar, MA; Álava-Rabasa, S; Albaladejo-Florín, MJ; Alexandra, AJE; Alfawares, R; Alferiev, IS; Alghamdi, HS; Ali, I; Allard, B; Allen, JD; Almada, E; Alobaid, A; Alonso, GL; Alqahtani, YS; Alqarawi, W; Alsaleh, H; Alyami, BA; Amaral, BPD; Amaro, JT; Amin, SAW; Amodio, E; Amoo, ZA; Andia Biraro, I; Angiolella, L; Anheyer, D; Anlay, DZ; Annex, BH; Antonio-Aguirre, B; Apple, S; Arbuznikov, AV; Arinsoy, T; Armstrong, DK; Ash, S; Aslam, M; Asrie, F; Astur, DC; Atzrodt, J; Au, DW; Aucoin, M; Auerbach, EJ; Azarian, S; Ba, D; Bai, Z; Baisch, PRM; Balkissou, AD; Baltzopoulos, V; Banaszewski, M; Banerjee, S; Bao, Y; Baradwan, A; Barandika, JF; Barger, PM; Barion, MRL; Barrett, CD; Basudan, AM; Baur, LE; Baz-Rodríguez, SA; Beamer, P; Beaulant, A; Becker, DF; Beckers, C; Bedel, J; Bedlack, R; Bermúdez de Castro, JM; Berry, JD; Berthier, C; Bhattacharya, D; Biadgo, B; Bianco, G; Bianco, M; Bibi, S; Bigliardi, AP; Billheimer, D; Birnie, DH; Biswas, K; Blair, HC; Bognetti, P; Bolan, PJ; Bolla, JR; Bolze, A; Bonnaillie, P; Borlimi, R; Bórquez, J; Bottari, NB; Boulleys-Nana, JR; Brighetti, G; Brodeur, GM; Budnyak, T; Budnyk, S; Bukirwa, VD; Bulman, DM; Burm, R; Busman-Sahay, K; Butcher, TW; Cai, C; Cai, H; Cai, L; Cairati, M; Calvano, CD; Camacho-Ordóñez, A; Camela, E; Cameron, T; Campbell, BS; Cansian, RL; Cao, Y; Caporale, AS; Carciofi, AC; Cardozo, V; Carè, J; Carlos, AF; Carozza, R; Carroll, CJW; Carsetti, A; Carubelli, V; Casarotta, E; Casas, M; Caselli, G; Castillo-Lora, J; Cataldi, TRI; Cavalcante, ELB; Cavaleiro, A; Cayci, Z; Cebrián-Tarancón, C; Cedrone, E; Cella, D; Cereda, C; Ceretti, A; Ceroni, M; Cha, YH; Chai, X; Chang, EF; Chang, TS; Chanteux, H; Chao, M; Chaplin, BP; Chaturvedi, S; Chaturvedi, V; Chaudhary, DK; Chen, A; Chen, C; Chen, HY; Chen, J; 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Langaro, MC; Langham, MC; Lao, X; Larocca, MC; Lassus, J; Lattimer, TA; Lazar, S; Le, MH; Leal, DB; Leal, M; Leary, A; Ledermann, JA; Lee, JF; Lee, MV; Lee, NH; Leeds, CM; Leeds, JS; Lefrandt, JD; Leicht, AS; Leonard, M; Lev, S; Levy, K; Li, B; Li, C; Li, CM; Li, DH; Li, H; Li, J; Li, L; Li, LJ; Li, N; Li, P; Li, T; Li, X; Li, XH; Li, XQ; Li, XX; Li, Y; Li, Z; Li, ZY; Liao, YF; Lin, CC; Lin, MH; Lin, Y; Ling, Y; Links, TP; Lira-Romero, E; Liu, C; Liu, D; Liu, H; Liu, J; Liu, L; Liu, LP; Liu, M; Liu, T; Liu, W; Liu, X; Liu, XH; Liu, Y; Liuwantara, D; Ljumanovic, N; Lobo, L; Lokhande, K; Lopes, A; Lopes, RMRM; López-Gutiérrez, JC; López-Muñoz, MJ; López-Santamaría, M; Lorenzo, C; Lorusso, D; Losito, I; Lu, C; Lu, H; Lu, HZ; Lu, SH; Lu, SN; Lu, Y; Lu, ZY; Luboga, F; Luo, JJ; Luo, KL; Luo, Y; Lutomski, CA; Lv, W; M Piedade, MF; Ma, J; Ma, JQ; Ma, JX; Ma, N; Ma, P; Ma, S; Maciel, M; Madureira, M; Maganaris, C; Maginn, EJ; Mahnashi, MH; Maierhofer, M; Majetschak, M; Malla, TR; Maloney, L; Mann, DL; Mansuri, A; Marelli, E; Margulis, CJ; Marrella, A; Martin, BL; Martín-Francés, L; Martínez de Pinillos, M; Martínez-Navarro, EM; Martinez-Quintanilla Jimenez, D; Martínez-Velasco, A; Martínez-Villaseñor, L; Martinón-Torres, M; Martins, BA; Massongo, M; Mathew, AP; Mathews, D; Matsui, J; Matsumoto, KI; Mau, T; Maves, RC; Mayclin, SJ; Mayer, JM; Maynard, ND; Mayr, T; Mboowa, MG; McEvoy, MP; McIntyre, RC; McKay, JA; McPhail, MJW; McVeigh, AL; Mebazaa, A; Medici, V; Medina, DN; Mehmood, T; Mei-Li, C; Melku, M; Meloncelli, S; Mendes, GC; Mendoza-Velásquez, C; Mercadante, R; Mercado, MI; Merenda, MEZ; Meunier, J; Mi, SL; Michels, M; Mijatovic, V; Mikhailov, V; Milheiro, SA; Miller, DC; Ming, F; Mitsuishi, M; Miyashita, T; Mo, J; Mo, S; Modesto-Mata, M; Moeller, S; Monte, A; Monteiro, L; Montomoli, J; Moore, EE; Moore, HB; Moore, PK; Mor, MK; Moratalla-López, N; Moratilla Lapeña, L; Moreira, R; Moreno, MA; Mörk, AC; Morton, M; Mosier, JM; Mou, LH; Mougharbel, AS; Muccillo-Baisch, AL; Muñoz-Serrano, AJ; Mustafa, B; Nair, GM; Nakanishi, I; Nakanjako, D; Naraparaju, K; Nawani, N; Neffati, R; Neil, EC; Neilipovitz, D; Neira-Borrajo, I; Nelson, MT; Nery, PB; Nese, M; Nguyen, F; Nguyen, MH; Niazy, AA; Nicolaï, J; Nogueira, F; Norbäck, D; Novaretti, JV; O'Donnell, T; O'Dowd, A; O'Malley, DM; Oaknin, A; Ogata, K; Ohkubo, K; Ojha, M; Olaleye, MT; Olawande, B; Olomo, EJ; Ong, EWY; Ono, A; Onwumere, J; Ortiz Bibriesca, DM; Ou, X; Oza, AM; Ozturk, K; Özütemiz, C; Palacio-Pastrana, C; Palaparthi, A; Palevsky, PM; Pan, K; Pantanetti, S; Papachristou, DJ; Pariani, A; Parikh, CR; Parissis, J; Paroul, N; Parry, S; Patel, N; Patel, SM; Patel, VC; Pawar, S; Pefura-Yone, EW; Peixoto Andrade, BCO; Pelepenko, LE; Peña-Lora, D; Peng, S; Pérez-Moro, OS; Perez-Ortiz, AC; Perry, LM; Peter, CM; Phillips, NJ; Phillips, P; Pia Tek, J; Piner, LW; Pinto, EA; Pinto, SN; Piyachaturawat, P; Poka-Mayap, V; Polledri, E; Poloni, TE; Ponessa, G; Poole, ST; Post, AK; Potter, TM; Pressly, BB; Prouty, MG; Prudêncio, M; Pulkki, K; Pupier, C; Qian, H; Qian, ZP; Qiu, Y; Qu, G; Rahimi, S; Rahman, AU; Ramadan, H; Ramanna, S; Ramirez, I; Randolph, GJ; Rasheed, A; Rault, J; Raviprakash, V; Reale, E; Redpath, C; Rema, V; Remucal, CK; Remy, D; Ren, T; Ribeiro, LB; Riboli, G; Richards, J; Rieger, V; Rieusset, J; Riva, A; Rivabella Maknis, T; Robbins, JL; Robinson, CV; Roche-Campo, F; Rodriguez, R; Rodríguez-de-Cía, J; Rollenhagen, JE; Rosen, EP; Rub, D; Rubin, N; Rubin, NT; Ruurda, JP; Saad, O; Sabell, T; Saber, SE; Sabet, M; Sadek, MM; Saejio, A; Salinas, RM; Saliu, IO; Sande, D; Sang, D; Sangenito, LS; Santos, ALSD; Sarmiento Caldas, MC; Sassaroli, S; Sassi, V; Sato, J; Sauaia, A; Saunders, K; Saunders, PR; Savarino, SJ; Scambia, G; Scanlon, N; Schetinger, MR; Schinkel, AFL; Schladweiler, MC; Schofield, CJ; Schuepbach, RA; Schulz, J; Schwartz, N; Scorcella, C; Seeley, J; Seemann, F; Seinige, D; Sengoku, T; Seravalli, J; Sgromo, B; Shaheen, MY; Shan, L; Shanmugam, S; Shao, H; Sharma, S; Shaw, KJ; Shen, BQ; Shen, CH; Shen, P; Shen, S; Shen, Y; Shen, Z; Shi, J; Shi-Li, L; Shimoda, K; Shoji, Y; Shun, C; Silva, MA; Silva-Cardoso, J; Simas, NK; Simirgiotis, MJ; Sincock, SA; Singh, MP; Sionis, A; Siu, J; Sivieri, EM; Sjerps, MJ; Skoczen, SL; Slabon, A; Slette, IJ; Smith, MD; Smith, S; Smith, TG; Snapp, KS; Snow, SJ; Soares, MCF; Soberman, D; Solares, MD; Soliman, I; Song, J; Sorooshian, A; Sorrell, TC; Spinar, J; Staudt, A; Steinhart, C; Stern, ST; Stevens, DM; Stiers, KM; Stimming, U; Su, YG; Subbian, V; Suga, H; Sukhija-Cohen, A; Suksamrarn, A; Suksen, K; Sun, J; Sun, M; Sun, P; Sun, W; Sun, XF; Sun, Y; Sundell, J; Susan, LF; Sutjarit, N; Swamy, KV; Swisher, EM; Sykes, C; Takahashi, JA; Talmor, DS; Tan, B; Tan, ZK; Tang, L; Tang, S; Tanner, JJ; Tanwar, M; Tarazi, Z; Tarvasmäki, T; Tay, FR; Teketel, A; Temitayo, GI; Thersleff, T; Thiessen Philbrook, H; Thompson, LC; Thongon, N; Tian, B; Tian, F; Tian, Q; Timothy, AT; Tingle, MD; Titze, IR; Tolppanen, H; Tong, W; Toyoda, H; Tronconi, L; Tseng, CH; Tu, H; Tu, YJ; Tung, SY; Turpault, S; Tuynman, JB; Uemoto, AT; Ugurlu, M; Ullah, S; Underwood, RS; Ungell, AL; Usandizaga-Elio, I; Vakonakis, I; van Boxel, GI; van den Beucken, JJJP; van der Boom, T; van Slegtenhorst, MA; Vanni, JR; Vaquera, A; Vasconcellos, RS; Velayos, M; Vena, R; Ventura, G; Verso, MG; Vincent, RP; Vitale, F; Vitali, S; Vlek, SL; Vleugels, MPH; Volkmann, N; Vukelic, M; Wagner Mackenzie, B; Wairagala, P; Waller, SB; Wan, J; Wan, MT; Wan, Y; Wang, CC; Wang, H; Wang, J; Wang, JF; Wang, K; Wang, L; Wang, M; Wang, S; Wang, WM; Wang, X; Wang, Y; Wang, YD; Wang, YF; Wang, Z; Wang, ZG; Warriner, K; Weberpals, JI; Weerachayaphorn, J; Wehrli, FW; Wei, J; Wei, KL; Weinheimer, CJ; Weisbord, SD; Wen, S; Wendel Garcia, PD; Williams, JW; Williams, R; Winkler, C; Wirman, AP; Wong, S; Woods, CM; Wu, B; Wu, C; Wu, F; Wu, P; Wu, S; Wu, Y; Wu, YN; Wu, ZH; Wurtzel, JGT; Xia, L; Xia, Z; Xia, ZZ; Xiao, H; Xie, C; Xin, ZM; Xing, Y; Xing, Z; Xu, S; Xu, SB; Xu, T; Xu, X; Xu, Y; Xue, L; Xun, J; Yaffe, MB; Yalew, A; Yamamoto, S; Yan, D; Yan, H; Yan, S; Yan, X; Yang, AD; Yang, E; Yang, H; Yang, J; Yang, JL; Yang, K; Yang, M; Yang, P; Yang, Q; Yang, S; Yang, W; Yang, X; Yang, Y; Yao, JC; Yao, WL; Yao, Y; Yaqub, TB; Ye, J; Ye, W; Yen, CW; Yeter, HH; Yin, C; Yip, V; Yong-Yi, J; Yu, HJ; Yu, MF; Yu, S; Yu, W; Yu, WW; Yu, X; Yuan, P; Yuan, Q; Yue, XY; Zaia, AA; Zakhary, SY; Zalwango, F; Zamalloa, A; Zamparo, P; Zampini, IC; Zani, JL; Zeitoun, R; Zeng, N; Zenteno, JC; Zepeda-Palacio, C; Zhai, C; Zhang, B; Zhang, G; Zhang, J; Zhang, K; Zhang, Q; Zhang, R; Zhang, T; Zhang, X; Zhang, Y; Zhang, YY; Zhao, B; Zhao, D; Zhao, G; Zhao, H; Zhao, Q; Zhao, R; Zhao, S; Zhao, T; Zhao, X; Zhao, XA; Zhao, Y; Zhao, Z; Zheng, Z; Zhi-Min, G; Zhou, CL; Zhou, HD; Zhou, J; Zhou, W; Zhou, XQ; Zhou, Z; Zhu, C; Zhu, H; Zhu, L; Zhu, Y; Zitzmann, N; Zou, L; Zou, Y, 2022
)
0.72
"Dose adjustments for individual drugs are not necessary with combined dosing of anaprazole, amoxicillin, clarithromycin and bismuth."( Pharmacokinetic Interaction of Anaprazole, Amoxicillin and Clarithromycin after Single-Dose Simultaneous Administration and the Effect of Adding Bismuth on Their Pharmacokinetics in Healthy Male Chinese Subjects.
Chen, J; Ding, S; Li, T; Liu, Y; Shao, F; Wang, L; Xie, L; Zhang, Z; Zhou, C; Zhou, S; Zhu, B; Zhu, J, 2023
)
0.91
" This study aimed to evaluate the efficacy and safety of 10-day vonoprazan-amoxicillin dual therapy as a first-line treatment of Helicobacter pylori infection compared with B-quadruple and to explore the optimal dosage of amoxicillin in the dual therapy."( Ten-Day Vonoprazan-Amoxicillin Dual Therapy as a First-Line Treatment of Helicobacter pylori Infection Compared With Bismuth-Containing Quadruple Therapy.
Dang, YN; Gao, X; Li, LR; Li, WJ; Li, X; Qian, HS; Xu, XB; Yang, Z; Yuan, L; Zhang, GX; Zhang, M; Zhang, WF, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Occurs in Manufacturing (2 Product(s))

Product Categories

Product CategoryProducts
Vitamins & Supplements2

Products

ProductBrandCategoryCompounds Matched from IngredientsDate Retrieved
Heaven Sent Wellgenix Balanced Essentials + Plus Liquid Vitamins Berry -- 32 fl ozHeaven SentVitamins & Supplementscitric acid, Antimony, Arginine, Vitamin C, Aspartic Acid, Kelp, Barium, Beryllium, Biotin, Bismuth, Boron, Bromide, Omega 3, Cerium, Cesium, Chromium, citric acid, Cobalt, Cystine, Vitamin E, fructose, Dysprosium, Erbium, Europium, Fluoride, Folate, Gadolinium, Gallium, Vitamin E, Glycine, Gold, Hafnium, Histidine, Holmium, Inositol, Iodine, Iodine, Isoleucine, Lanthanum, Leucine, Calcium Carbonate, Lithium, Lutetium, Lysine, Manganese, Methionine, Molybdenum, Neodymium, Niacin, Nickel, Niobium, Pantothenic Acid, Phenylalanine, Phosphorus, Praseodymium, Proline, Vitamin B6, Vitamin A, Rhenium, Riboflavin, Rubidium, Samarium, Scandium, Selenium, Serine, Silicon, Silver, Strontium, Tantalum, Tellurium, Terbium, Thallium, Thiamin, Thorium, Threonine, Thulium, Tin, Titanium, Tryptophan, Tungsten, Tyrosine, Valine, Vanadium, Vitamin B12, Vitamin B6, Vitamin K, Ytterbium, Yttrium, Zirconium2024-11-29 10:47:42
Olympian Labs Sea Nourishment Cran-Raspberry -- 32 fl ozOlympian LabsVitamins & SupplementsLipase, citric acid, Alanine, Arginine, Vitamin C, Aspartic Acid, Barium, Beta Carotene, Bismuth, Boron, Bromine, Cadmium, Cellulase, Cesium, Chloride, Chromium, citric acid, Citrulline, Cobalt, Cysteine, Cystine, Vitamin E, fructose, Germanium, Vitamin E, Glutamine, Glycine, Gold, Histidine, Hydrogen, Indium, Iodine, Iridium, Lanthanum, Lithium, Manganese, Molybdenum, Vitamin B, Nickel, Niobium, Ornithine, Osmium, Palladium, Phosphorus, Platinum, Proline, Rhodium, Rubidium, Selenium, Serine, Silver, Strontium, Sulfur, Taurine, Tellurium, Thallium, Tin, Titanium, Tungsten, CoQ7, CoQ8, CoQ9, Uranium, Vanadium2024-11-29 10:47:42

Drug Classes (2)

ClassDescription
pnictogenAny p-block element atom that is in group 15 of the periodic table: nitrogen, phosphorus, arsenic, antimony and bismuth.
metal atomAn atom of an element that exhibits typical metallic properties, being typically shiny, with high electrical and thermal conductivity.
[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]

Research

Studies (6,194)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901998 (32.26)18.7374
1990's927 (14.97)18.2507
2000's984 (15.89)29.6817
2010's1611 (26.01)24.3611
2020's674 (10.88)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials671 (10.07%)5.53%
Reviews526 (7.90%)6.00%
Case Studies237 (3.56%)4.05%
Observational10 (0.15%)0.25%
Other5,218 (78.32%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (143)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Antibiotic Susceptibility-based Tailored Therapy for Helicobacter Pylori Treatment in Patients With Penicillin Allergy: a Prospective Clinical Trial [NCT03708848]Phase 4112 participants (Actual)Interventional2018-12-05Completed
Rescue Therapy for Helicobacter Pylori Eradication: A Randomized Non-Inferiority Trial of Minocycline or Tetracycline in Bismuth Quadruple Therapy [NCT04531059]Phase 4368 participants (Actual)Interventional2020-10-15Completed
Helicobacter Pylori Eradication Using a Bismuth Quadruple Therapy Among Asymptomatically Infected Adults in El Paso, Texas: A Pilot Study. [NCT01335334]Phase 450 participants (Anticipated)Interventional2011-03-31Recruiting
Twice-a-day PPI, Tetracycline, Metronidazolequadruple Therapy With Pylera® or Lactobacillus Reuteri for Treatment naïve or for Retreatment of H. Pylori: Two Randomized Pilot Studies [NCT03925818]99 participants (Actual)Interventional2017-08-29Terminated(stopped due to Lactobacillus reuteri (Gastrus®) was not anymore available in the region)
The Efficacy of Bismuth-containing Quadruple Therapy in the First-line Treatment of Helicobacter Pylori Infection in 10 Days and 14 Days: a Prospective, Randomized, Controlled Study [NCT05586113]Phase 4398 participants (Anticipated)Interventional2023-02-06Not yet recruiting
Rescue Therapy for Helicobacter Pylori Eradication: A Randomized and Non-inferiority Trail of High-dose Esomeprazole and Amoxicillin Dual Therapy Versus Bismuth-containing Quadruple Therapy [NCT04678492]Phase 4658 participants (Actual)Interventional2020-12-20Completed
THE EFFECT OF HELICOBACTER PYLORI ERADICATION THERAPY TO GASTRIC WALL THICKNESS BEFORE THE LAPAROSCOPIC SLEEVE GASTRECTOMY [NCT03757650]Phase 43 participants (Actual)Interventional2018-10-01Completed
Analysis of the Impact of Helicobacter Pylori Infection and Eradication on Salivary Microbiome in Adults by 16S Pyrosequencing [NCT03730766]Phase 460 participants (Anticipated)Interventional2018-08-01Recruiting
Helicobacter Pylori Eradication Rates of Bismuth-containing Quadruple Therapy vs Modified Quadruple Therapy in Korea; Open-label, Randomized Controlled Trial [NCT03665428]Phase 4233 participants (Actual)Interventional2018-07-16Completed
Rescue Therapy for Helicobacter Pylori Eradication: A Randomized and Non-inferiority Trail of Berberine Plus Amoxicillin Quadruple Therapy Versus Tetracycline Plus Furazolidone Quadruple Therapy [NCT03609892]Phase 4658 participants (Actual)Interventional2018-08-01Completed
A Prospective, Single-center, Open-label, Clinical Trial to Compare the 10-day Sequential Therapy and 7-day Culture Based Tailored Therapy for the Eradication of Helicobacter Pylori [NCT02373280]600 participants (Anticipated)Interventional2014-08-31Recruiting
Efficacies of Antimicrobial Susceptibility-Guided Versus Empirical Therapy for Rescue Treatment of Helicobacter Pylori Infection-A Randomized Clinical Trial [NCT03658746]Phase 4420 participants (Actual)Interventional2019-01-01Completed
Bismuth-containing Quadruple Therapy for Helicobacter Pylori First-line Treatment: A Multicenter Randomized Clinical Trial of Different Tetracycline Doses and Frequencies. [NCT05431075]Phase 4407 participants (Anticipated)Interventional2022-07-31Not yet recruiting
Visiting Staff, Division of Gastroenterology and Department of Internal Medicine, Mackay Memorial Hospital, Taipei, Taiwan [NCT04853875]Phase 4104 participants (Actual)Interventional2021-04-19Completed
Comparison of Genotypic Resistance Guided Versus Susceptibility Testing Guided Therapy for the Third-line Eradication of H. Pylori- a Multicenter Randomized Trial [NCT03555526]Phase 4320 participants (Anticipated)Interventional2017-12-15Recruiting
Bismuth Quadruple Therapy for Helicobacter Pylori Rescue Therapy: A Multicenter Randomized Non-Inferiority Trial of Different Tetracycline Doses and Frequencies. [NCT05432115]Phase 4407 participants (Anticipated)Interventional2022-06-25Recruiting
A Randomized Double-Blind, Double-Dummy, Phase 3 Study to Evaluate the Efficacy and Safety of Oral TAK-438 20mg Compared to Lansoprazole 30mg Once- or Twice-Daily in the Treatment of Endoscopically Confirmed Gastric Ulcer Subjects With or Without Helicoba [NCT03050307]Phase 3234 participants (Actual)Interventional2017-04-17Completed
A Prospective, Single-center, Randomized, Open-label, Parallel Design Clinical Trial to Compare the 14-day Bismuth Quadruple Therapy and 7-day Culture Based Tailored Therapy for the Eradication of Helicobacter as a Rescue 2nd Therapy. [NCT02359331]370 participants (Actual)Interventional2014-08-31Terminated
10-Day Antimicrobial Susceptibility Testing Guided Triple Therapy Versus 14-Day Empirical Tailored Therapy for the First-line Treatment of Helicobacter Pylori Infection-A Randomized Controlled Trail [NCT03571230]Phase 4400 participants (Anticipated)Interventional2018-07-01Not yet recruiting
Prospective, Randomized Controlled Trial Comparing High Dose Amoxicillin Versus Tetracycline Based Quadruple Therapy as Second-line Treatment for Resistant Helicobacter Pylori Infection [NCT02175927]Phase 4312 participants (Actual)Interventional2014-07-31Completed
Bismuth Quadruple Therapy Versus Standard Triple Therapy for the First-line Treatment of Helicobacter Pylori Infection in Children: Efficacy and Safety [NCT06143124]Phase 4216 participants (Anticipated)Interventional2022-03-03Recruiting
Efficacy and Safety of a 14-day Modified Sequential Therapy for Refractory Helicobacter Pylori Infection: an Open Randomized Pilot Study [NCT03658733]Phase 4120 participants (Anticipated)Interventional2018-12-15Not yet recruiting
Gastrointestinal Preparation and Efficacy of Saccharomyces Boulardii as a Pre-treatment for Helicobacter Pylori Rescue Therapy [NCT05191875]106 participants (Actual)Interventional2021-12-01Completed
Efficacy and Safety of a 14-day Modified Sequential Therapy for Refractory Helicobacter Pylori Infection: a Pilot Study [NCT03616405]Phase 460 participants (Anticipated)Interventional2019-04-01Not yet recruiting
The Evaluation of Saccharomyces Boulardii Sachets Combined With Standard Quadruple Therapy for Eradication of Helicobacter Pylori: a Prospective, Multi-Center Trial [NCT03688828]360 participants (Actual)Interventional2018-11-11Completed
Crystalline Exposition During Pediatric Cranial CT Imaging [NCT03665181]23 participants (Actual)Observational2018-10-02Completed
A Randomized Double-Blind, Double-Dummy, Phase 3 Study to Evaluate the Efficacy and Safety of Oral TAK-438 20 mg Compared to Lansoprazole 30 mg Once- or Twice-Daily in the Treatment of Endoscopically Confirmed Duodenal Ulcer Subjects With or Without Helic [NCT03050359]Phase 3533 participants (Actual)Interventional2017-04-05Completed
A Real World Study of Bismuth Colloidal Pectin Granules Quadruple Therapy for H. Pylori Eradication [NCT04660123]Phase 4959 participants (Actual)Interventional2020-12-20Completed
A Prospective Double-blind, Randomized, Sham-controlled Trial to Evaluate the Effect of a Lead Free Drape on Scatter Radiation Exposure to Endoscopy Staff During Endoscopic Retrograde Cholangiopancreatography [NCT02063841]Early Phase 12 participants (Actual)Interventional2013-08-31Completed
Rifabutin-containing Triple Therapy for Helicobacter Pylori Rescue Treatment: a Randomized Controlled Trial [NCT05874544]Phase 4357 participants (Anticipated)Interventional2023-05-16Recruiting
Efficacy of Tailored for Helicobacter Pylori Rescue Treatment Based on Antimicrobial-susceptibility Testing [NCT03413020]Phase 4200 participants (Actual)Interventional2018-01-03Completed
A Phase 1, Double-Blind, Parallel Group Study to Evaluate the Safety and Pharmacokinetics of Quadruple Therapy (Bismuth, Clarithromycin, and Amoxicillin) With TAK-438 Versus Quadruple Therapy With Lansoprazole [NCT02892409]Phase 130 participants (Actual)Interventional2016-09-05Completed
Study on The Efficacy and Safety of Berberine,Amoxicillin and Vonoprazan Containing Triple Therapy in Helicobacter Pylori First-Line Eradication [NCT05014334]Phase 4300 participants (Actual)Interventional2021-12-01Completed
Efficacy and Safety of Berberine Hydrochloride, Amoxicillin and Rabeprazole Triple Therapy in the First Eradication of Helicobacter Pylori [NCT04697186]Phase 4524 participants (Actual)Interventional2021-01-07Completed
Optimized Bismuth Quadruple Therapy vs Triple Standard Therapy for Helicobacter Pylori Eradication: Clinical Efficacy Randomized Trial [NCT05664685]Phase 4204 participants (Anticipated)Interventional2022-10-17Recruiting
The Most Appropriate Prescription of the First-line, the Second-line, and the Third Treatment for H. Pylori Eradication Among Patients Who Are Comorbid Diabetes Mellitus, Chronic Obstructive Pulmonary Disease, or Chronic Kidney Disease [NCT05475431]1,000 participants (Anticipated)Observational2020-05-06Enrolling by invitation
Efficacy of Vonoprazan-containing Triple Therapy Versus Empiric Bismuth Quadruple Therapy for First-line Helicobacter Pylori Treatment: a Randomized Clinical Trial [NCT05726734]Phase 4100 participants (Anticipated)Interventional2023-02-06Not yet recruiting
[NCT02873065]Phase 40 participants Interventional2014-09-30Completed
Comparison of Efficacy of Bismuth Potassium Citrate, Pectin Bismuth Capsules, and Pectin Bismuth Granules in the Treatment of Helicobacter Pylori (Hp) First-line Quadruple Regimen: a Multicenter, Randomized, Prospective, Comparative Clinical Trial [NCT04209933]Phase 4240 participants (Actual)Interventional2020-05-25Completed
Efficacy and Safety of Quadruple Therapy by Bismuth Subcitrate Potassium, Metronidazole, and Tetracycline Given X 10 Days With Omeprazole in Eradication of Helicobacter Pylori: A Comparison to Omeprazole, Amoxicillin and Clarithromycin Given X 7 Days [NCT00669955]Phase 3440 participants (Actual)Interventional2008-06-30Completed
A Comparison of Four Different Treatment Regimens as the First-line Treatment of Helicobacter Pylori in Chinese Children and Investigation of Resistance and Impact factors-a Multicenter Study [NCT03365609]1,440 participants (Anticipated)Interventional2017-09-20Recruiting
Bismuth-Metronidazole Triple Versus Quadruple Therapy for Helicobacter Pylori First-line Treatment: A Randomized Controlled Trial [NCT04667299]Phase 4270 participants (Anticipated)Interventional2020-12-20Recruiting
Comparing the Efficacy and Impact on Gastrointestinal Microbiome of Reverse Hybrid Therapy and Bismuth Quadruple Therapy in Helicobacter Pylori Eradication [NCT02547038]352 participants (Actual)Interventional2015-02-28Completed
A Single-center, Randomized, Open-label, Crossover Study to Evaluate the Pharmacokinetic Drug-drug Interaction of the Quadruple Therapy With Anaprazole/Amoxicilin/Clarithromycin/Bismuth in Healthy Chinese Male Subjects [NCT04444011]Phase 132 participants (Anticipated)Interventional2020-07-01Not yet recruiting
Efficacy of High-dose Dual Therapy Versus Bismuth-containing Quadruple Therapy for First-line Treatment of Helicobacter Pylori Infection - A Prospective, Randomized, Comparative Study [NCT02483715]Phase 4589 participants (Actual)Interventional2015-07-31Completed
Randomized, Double-blind, Placebo-controlled Trial of the Impact of Bismuth Subsalicylate on Antimicrobial Use Among Adult Diarrhea Outpatients in Pakistan [NCT02047162]400 participants (Actual)Interventional2014-05-31Completed
Efficacy of 7-day Versus 14-day Bismuth Quadruple Therapy for the Eradication of Helicobacter Pylori : A Multicenter Randomized Non-Inferiority Trial [NCT05997433]254 participants (Anticipated)Interventional2023-09-02Recruiting
Effects of High-dose Dual Therapy and Bismuth Quadruple Therapy for Helicobacter Pylori Eradication on Intestinal Microecology [NCT05742568]Phase 4120 participants (Anticipated)Interventional2022-12-01Recruiting
Efficacy of High Dose of Amoxicillin And Metronidazole Plus Bismuth For Helicobacter Pylori Treatment In Naive Patients : A Randomized Clinical Trial [NCT03557437]Phase 4216 participants (Actual)Interventional2018-05-25Completed
An Open Randomized Controlled Study of Bismuth Quadruple Therapy With Cefuroxime as Rescue Therapy for Helicobacter Pylori Infection [NCT04723472]82 participants (Anticipated)Interventional2023-08-01Suspended(stopped due to Want to modify the study further)
Prospective, Randomized Controlled Trial Comparing Amoxicillin and Metronidazole Based Bismuth-containing Quadruple Therapy With Amoxicillin and Clarithromycin Based Quadruple Therapy for First-line Helicobacter Pylori Eradication [NCT02175901]Phase 4215 participants (Actual)Interventional2014-07-31Completed
Effect of Oral Helicobacter Pylori Infection on the Efficacy of Gastroluminal Helicobacter Pylori Eradication Therapy [NCT05790525]Phase 4200 participants (Anticipated)Interventional2022-11-22Recruiting
A Randomized Double-Blind, Phase 3 Study to Evaluate the Efficacy and Safety of Bismuth-Containing Quadruple Therapy With Oral TAK-438 20 mg Compared to Esomeprazole 20 mg Twice Daily in Subjects With Helicobacter Pylori Infection [NCT04198363]Phase 3510 participants (Actual)Interventional2020-04-30Completed
The Observation on the Efficacy of Dual Therapy Based on Vonoprazan in Eradicating Helicobacter Pylori [NCT06004401]400 participants (Anticipated)Interventional2023-08-20Not yet recruiting
An Exploratory Study of The Effect of Bismuth Subsalicylate on The Gut Microbiome and Host Response in Healthy Adults [NCT05930197]Phase 130 participants (Anticipated)Interventional2023-08-31Recruiting
A Randomized Clinical Trial of Clarithromycin/Bismuth Containing Quadruple Therapy for Helicobacter Pylori First-line Treatment [NCT02732249]Phase 466 participants (Actual)Interventional2016-04-01Completed
A Comparison of High-dose Dual Therapy and Half-dose Clarithromycin-containing Bismuth Quadruple Therapy for H.P Eradication in Elderly Patients [NCT04101708]Phase 4100 participants (Anticipated)Interventional2019-09-20Not yet recruiting
The Associations Between the Gastric Mucosal Pathology and the Eradication Rate of H.Pylori :A Multicenter Study [NCT04030715]1,200 participants (Anticipated)Interventional2018-09-01Recruiting
Comparison Between Tailored Therapy Guided by a Non-invasive Antibiotic Susceptibility Test and Empiric Treatment for First-line Helicobacter Pylori Eradication in Patients With Dyspepsia: a Randomized Controlled Trial. [NCT04107194]Phase 3362 participants (Anticipated)Interventional2020-01-14Recruiting
Efficacies of Susceptibility-guided vs Empiric Therapy for Rescue Treatment of Helicobacter Pylori Infection - A Prospective Randomized, Comparative Study [NCT05332444]Phase 4450 participants (Anticipated)Interventional2022-04-11Recruiting
Comparison of 7-day Proton Pump Inhibitor (PPI)-Clarithromycin Containing Triple Therapy and 10-day Bismuth Quadruple Therapy for Helicobacter Eradication as First-line Regimen: Randomized Controlled Trial [NCT02557932]Phase 3352 participants (Actual)Interventional2015-09-30Completed
Can Treatment With Bismuth Reduce Toxicity to Chemotherapy and Radiotherapy? A Clinical, Prospective, Randomized, Blinded Examination of Patients Suffering From Hematological Malignancies Treated With Intensive Chemotherapy and/or Radiotherapy. [NCT00892502]50 participants (Actual)Interventional2009-05-31Completed
Bismuth Quadruple Therapy in Helicobacter Pylori Rescue Therapy: A Multicenter Randomized Non-Inferiority Trial of Different Tetracycline Doses and Frequencies. [NCT05802888]Phase 4260 participants (Anticipated)Interventional2023-03-12Recruiting
Comparison of 7-day and 14-day Bismuth Based Quadruple Therapy for Secondary Helicobacter Pylori Eradication. [NCT00841854]Phase 4199 participants (Actual)Interventional2008-06-30Completed
Efficacies of High-dose Dual Therapy With or Without Bismuth Versus Amoxicillin-metronidazole Bismuth Quadruple Therapy for First-line Helicobacter Pylori Eradication - A Prospective, Randomized, Comparative Study [NCT03897244]Phase 4702 participants (Anticipated)Interventional2019-05-30Recruiting
Proton Pump Inhibitors and the Risk of Hospitalization for Community-acquired Pneumonia: Replicated Cohort Studies With Meta-analysis [NCT02555852]4,238,504 participants (Actual)Observational2011-09-30Completed
Helicobacter Pylori Eradication and Follow-up in Zhongshan Hospital [NCT05061732]Phase 44,447 participants (Anticipated)Interventional2021-09-30Recruiting
Rescue Therapy for Helicobacter Pylori Eradication: A Randomized and Non-inferiority Trail of Vonorazon and Amoxicillin Dual Therapy Versus Bismuth-containing Quadruple Therapy [NCT06168084]Phase 4688 participants (Anticipated)Interventional2023-06-06Recruiting
The Effect of Helicobacter Pylori Eradication on Liver Fat Content in Subjects With Non-alcoholic Fatty Liver Disease [NCT01876108]Phase 2100 participants (Anticipated)Interventional2012-07-31Completed
Comparison of the Efficacy of Clarithromycin-based Triple Therapy Versus Quadruple Therapies in the First Line Therapy of Helicobacter Pylori Infection- A Multicenter Randomized Comparative Trial [NCT01906879]Phase 41,620 participants (Anticipated)Interventional2013-06-30Recruiting
A Multicenter, Double Blind, Placebo-Controlled Study of Pepto-Bismol® (Bismuth Subsalicylate) on Gastrointestinal Tolerability in Healthy Volunteers Receiving Oral TECFIDERA™ (Dimethyl Fumarate) Delayed-Release Capsules Twice Daily [NCT01915901]Phase 1175 participants (Actual)Interventional2013-08-31Completed
Comparison of the Efficacy of Levofloxacin-based Sequential Therapy and Bismuth Quadruple Therapy in the Second Line and Third Line Therapy for Helicobacter Pylori Infection- A Multi-center Randomized Trial [NCT03148366]Phase 3560 participants (Actual)Interventional2015-02-28Completed
Phytomedicine-based and Quadruple Therapies in Helicobacter Pylori Infection. A Comparative Randomized Trial [NCT02004197]Phase 2/Phase 3176 participants (Actual)Interventional2010-01-31Completed
Doxycycline- and Furazolidone-containing Quadruple Regimen is Superior of Tailored Therapy as Rescue Treatment for Helicobacter Pylori Infection After Failure of Several Therapy [NCT02894268]Phase 4300 participants (Anticipated)Interventional2016-02-29Recruiting
An Open-Label, Randomized, Crossover Study to Evaluate the Pharmacokinetic Interaction After Multiple Oral Doses of Tegoprazan, Metronidazole, Tetracycline and Bismuth in Healthy Volunteers [NCT04066257]Phase 132 participants (Actual)Interventional2019-01-17Completed
Helicobacter Pylori Eradication With Berberine Hydrochloride, Lansoprazole, Amoxicillin and Bismuth Versus Clarithromycin Bismuth, Lansoprazole and Amoxicillin: A Randomized, Open-label, Non-inferiority, Phase Ⅳ Trial [NCT02633930]Phase 4566 participants (Actual)Interventional2015-12-31Completed
A Study on the Efficacy and Safety of Egg Yolk Antibody in Adjuvant Treatment of Helicobacter Pylori Infection [NCT05410223]100 participants (Anticipated)Interventional2021-04-06Recruiting
Comparison of Hybrid and Bismuth Containing Quadruple Therapies for Helicobacter Pylori Eradication: a Randomized Controlled Trial [NCT02541864]330 participants (Actual)Interventional2013-07-31Completed
Phase IV, Multicenter, Open Label, Randomized Study in Parallel Groups To Assess The Efficacy And Safety Of Bismuth Tripotassium Dicitrate (De-Nol®) In Combination With Pantoprazole And Pantoprazole Monotherapy In Treatment Of Patients With NSAID Induced [NCT02788123]Phase 49 participants (Actual)Interventional2017-03-03Terminated(stopped due to Internal reassessment of the medicinal product development strategy by Sponsor)
Susceptibility-Guided Sequential Therapy Versus Empirical Therapy for Helicobacter Pylori Infection: a Randomised Controlled Trial [NCT05549115]500 participants (Anticipated)Interventional2022-09-20Recruiting
Helicobacter Pylori Eradication Clostridium Butyricum Capsule and Bacillus Coagulans Tablets With Hydrochloride,Esomeprazole,Amoxicillin and Bismuth-containing Quadruple Therapy: a Randomized,Single-center,Open-label,Phase Ⅳ Trail [NCT05237115]Phase 4600 participants (Actual)Interventional2020-05-05Completed
[NCT01481844]Phase 3101 participants (Actual)Interventional2011-11-30Completed
Quadruple Therapy Using Esomeprazole, Colloidal Bismuth Subcitrate, Amoxicillin-Clavulanate, and Furazolidone in Patients Who Failed to Eradicate H. Pylori With Triple Therapy [NCT00520949]176 participants (Actual)Interventional2006-10-31Completed
Efficacy of Antibiotic Susceptibility-based Tailored Versus Empiric Therapy for Helicobacter Pylori First-line Treatment:a Randomized Clinical Trial [NCT02935010]Phase 4382 participants (Actual)Interventional2017-02-05Completed
Intragastric pH and Bismuth Effect for H. Pylori Eradication [NCT02894892]21 participants (Actual)Interventional2016-11-15Completed
Rifabutin-containing Triple Therapy for Rescue Treatment of Helicobacter Pylori: A Randomized Clinical Trial [NCT04879992]413 participants (Actual)Interventional2021-05-07Completed
CURRENT PRACTICE STUDY OF ANTIBIOTIC TREATMENT OF GASTRIC MALT LYMPHOMA [NCT00002682]Phase 25 participants (Actual)Interventional1995-08-10Completed
The Evaluation of Triple Therapy With Vonoprazan, Amoxicillin and Bismuth for Eradication of Helicobacter Pylori: a Prospective, Multi-Center, Randomized Controlled Trial [NCT05189444]672 participants (Anticipated)Interventional2022-03-25Not yet recruiting
Bismuth-containing Quadruple Therapy for Helicobacter Pylori Eradication: A Multicenter Randomized Clinical Trial of 10 and 14 Days [NCT05049902]Phase 41,300 participants (Actual)Interventional2021-09-21Completed
Comparison of Vonoprazan Fumarate-based Triple Therapy Versus Proton Pump Inhibitor and Bismuth Based Quadruple Therapy in the Eradication of Helicobacter Pylori: a Single-center Prospective Open-label Controlled Study [NCT05097846]100 participants (Anticipated)Interventional2021-06-17Recruiting
Prospective Randomised Trial of First and Second Line Treatments of Helicobacter Pylori Infection in Slovenia [NCT04359966]560 participants (Anticipated)Interventional2020-05-10Not yet recruiting
Doxycycline-containing Bismuth Quadruple Therapy for Helicobacter Pylori Rescue Treatment: a Randomized Controlled Trial [NCT05874570]Phase 4368 participants (Anticipated)Interventional2023-06-20Recruiting
Can Use of Bismuth Subsalicylate in Clostridium Difficile Patients Decrease the Length of Stay and Time to Resolution of Symptoms [NCT03592082]Phase 40 participants (Actual)Interventional2018-03-01Withdrawn(stopped due to Investigator left institution)
Helicobacter Pylori Treatment [NCT01668927]Phase 4424 participants (Actual)Interventional2012-07-31Completed
Treatment of Microscopic Colitis (Collagenous Colitis and Lymphocytic Colitis) With Budesonide, Bismuth or Fiber [NCT00184171]105 participants (Actual)Interventional2001-11-30Terminated(stopped due to insufficient data quality)
Efficacy of Quadruple Therapy Based on Fecal Molecular Antimicrobial Susceptibility Tests as First-line Treatment for Helicobacter Pylori Infection [NCT05718609]Phase 4855 participants (Anticipated)Interventional2023-03-01Recruiting
Comparison of Different Helicobacter Pylori Detection Methods in Patients With Chronic Atrophic Gastritis [NCT04923113]281 participants (Actual)Interventional2021-06-28Completed
The HEART BREAK Study: Effects of Heart Imaging Radiation on DNA Double-Stranded Breaks in Blood Lymphocytes and Hair Follicle Cells [NCT02617888]228 participants (Actual)Interventional2011-03-31Completed
A Phase 1, Double-Blind, Parallel Group Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Quadruple Therapy (Bismuth, Clarithromycin, and Amoxicillin) With Vonoprazan Versus Quadruple Therapy With Esomeprazole [NCT04753437]Phase 144 participants (Actual)Interventional2021-04-06Completed
A Prospective, Multi-center, Randomized, Open-label, Parallel Design Clinical Trial to Compare 10-day Sequential Therapy and 14-day Modified Bismuth Quadruple Therapy for the Eradication of Helicobacter Pylori in Korea [NCT02159976]390 participants (Actual)Interventional2014-07-31Completed
Ten-day Amoxicillin-containing Dual Therapy as First-line Helicobacter Pylori Treatment in Elderly Patients: a Randomized Trial [NCT05419674]Phase 4393 participants (Anticipated)Interventional2022-08-01Recruiting
Comparing 10-day Reverse Hybrid Therapy and 10-day Triple Therapy Plus Bismuth Therapy on Helicobacter Pylori Eradication [NCT04566211]440 participants (Anticipated)Interventional2020-01-01Recruiting
[NCT01667575]Phase 4180 participants (Actual)Interventional2012-08-31Completed
Levofloxacin-containing Therapy for Helicobacter Pylori Treatment [NCT01667718]Phase 4161 participants (Actual)Interventional2012-05-31Completed
[NCT01742429]Phase 4200 participants (Actual)Interventional2012-11-30Completed
Standard or Short-course Vonoprazan Non-bismuth Triple Therapy or High-dose Dual Therapy Versus Rabeprazole-bismuth Quadruple Therapy for Primary Helicobacter Pylori Eradication: A Single-center, Randomised, Controlled Trial. [NCT06168214]Phase 41,404 participants (Anticipated)Interventional2023-09-04Recruiting
Ten Days Quadruple Versus Sequential Therapy as Empirical First and Second Line Treatment for Helicobacter Pylori Eradication: a Randomized Crossover Trial [NCT01760824]391 participants (Actual)Interventional2011-05-31Completed
The Effect and Safety of Jinghua Weikang Capsule Containing Quadruple Therapy for IgAN With Helicobacter Pylori Infection, a Randomized Pilot Study [NCT05320133]80 participants (Anticipated)Interventional2022-06-20Enrolling by invitation
Efficacy of Two Antimicrobial Susceptibility Testing Guided Antibiotic Selection Strategies in Salvage Helicobacter Pylori Treatment [NCT02988089]Phase 4480 participants (Anticipated)Interventional2017-04-20Recruiting
A Prospective Randomized Trial of Levofloxacin-amoxicillin Triple Therapy vs. Levofloxacin-tetracycline Quadruple Therapy in Second-line Helicobacter Pylori Treatment [NCT02978157]102 participants (Actual)Interventional2015-02-28Completed
Comparing the Efficacy of 14-day Therapy Doxycycline With Bismuth Subsalicylate Versus Levofloxacin With Tinidazole on Rate of Eradication of Helicobacter Pylori Infected Patients on Syrian Population [NCT04348786]Phase 478 participants (Actual)Interventional2019-02-01Completed
Phase I/II Trial Of Sequential Therapy With Cytarabine And Bismuth-213-Labeled HuM195 (Humanized Anti-CD33) In Patients With Advanced Myeloid Malignancies [NCT00014495]Phase 1/Phase 232 participants (Actual)Interventional2000-11-30Completed
The Effect of Different Time Intervals on Rescue Treatment of Helicobacter Pylori Infection: a Prospective, Multicenter Observational Study [NCT05620589]626 participants (Anticipated)Observational2022-11-11Not yet recruiting
Helicobacter Pylori and Body Iron in Adults [NCT03146325]Phase 40 participants (Actual)Interventional2012-11-30Withdrawn(stopped due to Study was not funded and PI has left the institution)
Effectiveness of Minocycline-Containing Bismuth Quadruple Therapy as First-Line Regimen for Helicobacter Pylori Eradication [NCT04558502]Phase 4339 participants (Anticipated)Interventional2022-01-05Not yet recruiting
The Clinical Trial on the Eradication of Helicobacter Pylori With Bismuth Agent Quadruple and Modified Ban Xia Xie Xin Decoction [NCT05586464]Phase 1600 participants (Anticipated)Interventional2022-11-01Not yet recruiting
Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of Rifasutenizol (TNP 2198) in Combination With Rabeprazole and Amoxicillin in the Primary Treatment of Participants With H. Pylori Infection [NCT05857163]Phase 3700 participants (Anticipated)Interventional2023-05-18Recruiting
The Studies of Integrating Gastric and Gut Microbiota, F. Prausnitzii Metabolites, Microenvironment, and Epigenetics to Identify the Cancer Risk of H. Pylori-related Precancerous Conditions Through an AI System and Control the Risky by Probiotic Supplemen [NCT04527055]Phase 4312 participants (Anticipated)Interventional2020-05-06Enrolling by invitation
Vonoprazan Fumarate in Combination With Amoxicillin for the First-line Eradication - a Multicenter, Randomized, Parallel Controlled Study [NCT05196945]Phase 4316 participants (Anticipated)Interventional2022-03-31Not yet recruiting
A Phase II Clinical Trial of Anti-Helicobacter Pylori Treatment in Endoscopically Diagnosed Low-Grade Localized Gastric Lymphoma [NCT00003151]Phase 296 participants (Anticipated)Interventional1997-09-30Completed
Pilot and Randomized, Controlled Studies to Assess Stool Frequency of COVID + Patients Treated With Oral Bismuth Subsalicylate (Pepto-Bismol): SABER-C and Lite-SABER-C (Specific Administration of Bismuth for Early Recovery of COVID-19) [NCT04811339]Phase 460 participants (Actual)Interventional2020-10-27Completed
Helicobacter Pylori Eradication Therapy in Portugal: Prospective, Randomized, Blind and Multicentre Trial on the Efficacy of Quadruple Therapies and Their Clinical Impact, and Immunological and Gut Microbiota Changes [NCT05449028]230 participants (Anticipated)Interventional2022-05-01Recruiting
Efficacies of Hybrid, High-dose Dual and Bismuth Quadruple Therapies for the First-line Anti-H Pylori Treatment and Tetracycline-levofloxacin Quadruple Therapy for the Second-line Anti-H Pylori Treatment - a Multicentre Randomized Trial [NCT03779074]Phase 3918 participants (Actual)Interventional2018-09-03Completed
Personalized Treatment for Refractory H Pylori Infection [NCT02547025]126 participants (Actual)Interventional2012-08-01Completed
Compare 14-day Reverse Hybrid Therapy and 14-day Triple Therapy Plus Bismuth on Helicobacter Pylori Eradication [NCT03321773]440 participants (Anticipated)Interventional2017-01-31Recruiting
Efficacy of High-dose Dual Therapy Versus Bismuth-containing Quadruple Therapy for Rescue Treatment of Helicobacter Pylori Infection - A Prospective, Randomized, Comparative Study [NCT02490839]Phase 4450 participants (Actual)Interventional2015-07-31Completed
Adding Bismuth to Rabeprazole-based First-line Triple Therapy Does Not Improve the Eradication of Helicobacter Pylori [NCT03108287]Phase 4162 participants (Actual)Interventional2013-04-01Completed
Clarithromycin-, Metronidazole-, or Levofloxacin-containing Therapy for Helicobacter Pylori-infected Penicillin-allergic Patients: A Randomized Controlled Trial [NCT05023577]Phase 4504 participants (Anticipated)Interventional2021-08-26Recruiting
An Open-label, Fixed-sequence Study to Evaluate the Drug-drug Interactions Between Tegoprazan Tablets and Bismuth Potassium Citrate Capsules, Amoxicillin Capsules, and Clarithromycin Tablets in Healthy Subjects [NCT05915871]Phase 122 participants (Actual)Interventional2023-03-23Completed
Proton Pump Inhibitor and Amoxicillin Combined Bismuth or Metronidazole for Helicobacter Pylori First-line Treatment: A Randomized Controlled Trial [NCT05014685]Phase 4732 participants (Anticipated)Interventional2021-08-20Recruiting
Efficacy of High Dose of Dual Therapy Plus Bismuth for Helicobacter Pylori Treatment:a Randomized Clinical Trial [NCT03405584]Phase 4160 participants (Actual)Interventional2018-01-03Completed
Comparison of the Efficacy of Sequential Therapy and Bismuth Quadruple Therapy in the First Line and Second Line Therapy for Helicobacter Pylori Infection- A Multi-center Randomized Trial [NCT03156855]Phase 4620 participants (Anticipated)Interventional2015-09-30Recruiting
Bismuth Subsalicylate's Role in the Prevention of Travelers' Diarrhea and Impact on Acquisition of Gut Antimicrobial Resistance Genes [NCT03535272]Phase 3482 participants (Anticipated)Interventional2018-05-20Recruiting
Effect of Helicobacter Pylori Eradication on Gastric Cancer Prevention in Korea: a Randomized Controlled Clinical Trial [NCT02112214]Phase 35,224 participants (Anticipated)Interventional2014-06-30Active, not recruiting
Efficacy and Safety of Furazolidone-based Quadruple Therapy With Vonoprazan as First-line Treatment for Helicobacter Pylori Eradication: A Prospective Randomized Trial [NCT04907747]Phase 4234 participants (Anticipated)Interventional2021-05-18Recruiting
Bismuth-containing Quadruple Therapy for Helicobacter Pylori Eradication: A Multicenter Randomized Clinical Trial of 10 and 14 Days [NCT04901117]Phase 41,300 participants (Anticipated)Interventional2021-06-30Not yet recruiting
Bismuth Quadruple Therapy With Tetracycline Versus Doxycycline as Rescue Therapy for Helicobacter Pylori Infection: a Randomized Controlled Trial [NCT05018923]Phase 4242 participants (Anticipated)Interventional2021-08-24Recruiting
A Randomized, Placebo- and Benchmark-controlled, Double-blind Clinical Trial of Anusol Topical Ointment to Evaluate Symptom Relief in Patients With Haemorrhoids [NCT05157711]Phase 366 participants (Actual)Interventional2021-11-25Completed
Eradication Efficacy and Safety of High-dose Dual Therapy Compared With Furazolidone-based Quadruple Therapy as a Rescue Treatment for Helicobacter Pylori Infection: a Randomized Controlled Trial [NCT05176821]186 participants (Anticipated)Interventional2021-01-01Recruiting
Clinical Efficacy and Health Economic Evaluation of Susceptibility-Guided Therapy for Helicobacter Pylori Infection Treatment:Multicenter Randomized Controlled Study [NCT05250050]Phase 4388 participants (Anticipated)Interventional2022-03-25Recruiting
Helicobacter Pylori Eradication With Berberine Hydrochloride,Esomeprazole,Amoxicillin and Clarithromycin Versus Bismuth,Esomeprazole,Amoxicillin,and Clarithromycin: a Randomized,Open-label, Non-inferiority, Phase Ⅳ Trail [NCT02296021]Phase 4612 participants (Actual)Interventional2014-11-30Completed
Qingre Huashi Granules Combined the Modified Dual Therapy for Helicobacter Pylori Infection Treatment in the Elderly Patient, a Multi-center, Randomized, Controlled Trial [NCT05364619]160 participants (Anticipated)Interventional2022-08-05Recruiting
A Prospective Open-label Study on Efficacy and Tolerability of Colloidal Bismuth Sub-citrate as Adjunctive Therapy to a Combination of Esomeprazole, Amoxicillin and Metronidazole for 10 Days for Helicobacter Pylori Elimination in Children [NCT03299725]Phase 4120 participants (Anticipated)Interventional2017-11-24Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00014495 (1) [back to overview]Maximum Tolerated Dose
NCT00669955 (7) [back to overview]Number of Patients Experiencing Treatment Emergent Adverse Events.
NCT00669955 (7) [back to overview]H. Pylori Eradication and Presence or Past History of Peptic Ulcers
NCT00669955 (7) [back to overview]Helicobacter Pylori Eradication Confirmed by Urea Breath Test
NCT00669955 (7) [back to overview]Metronidazole Resistance
NCT00669955 (7) [back to overview]Overall Compliance to Study Medications
NCT00669955 (7) [back to overview]Number of Patients With Bismuth Plasma Concentrations Above the Toxic Level
NCT00669955 (7) [back to overview]Clarithromycin Resistance
NCT02159976 (4) [back to overview]Counts of Participants Whose Drug Compliance is More Than 85%
NCT02159976 (4) [back to overview]Counts of Participants With Adverse Event
NCT02159976 (4) [back to overview]Counts of Participants With Successful H. Pylori Eradication
NCT02159976 (4) [back to overview]Functional Dyspepsia Symptom Responses Rate
NCT02541864 (1) [back to overview]Number of Participants in Which H. Pylori Was Eradicated
NCT02547038 (1) [back to overview]Number of Participants in Which H. Pylori Was Eradicated
NCT02617888 (1) [back to overview]Number of Excess Double-strand DNA Break Foci Per Cell in Peripheral Blood Samples Post-imaging
NCT02892409 (8) [back to overview]Aeτ: Amount of Drug Excreted in Urine During a Dosing Interval for Bismuth
NCT02892409 (8) [back to overview]AUCτ: Area Under the Plasma Concentration-time Curve From Time 0 to Time Tau Over the Dosing Interval for Bismuth
NCT02892409 (8) [back to overview]Cmax: Maximum Observed Plasma Concentration for Bismuth
NCT02892409 (8) [back to overview]Percentage of Participants Who Discontinue Due to an Adverse Event (AE)
NCT02892409 (8) [back to overview]Percentage of Participants Who Experience at Least One Treatment Emergent Adverse Event (TEAE)
NCT02892409 (8) [back to overview]Percentage of Participants Who Meet the Markedly Abnormal Criteria for Safety Electrocardiogram (ECG) Parameters at Least Once Post-dose
NCT02892409 (8) [back to overview]Percentage of Participants Who Meet the Markedly Abnormal Criteria for Safety Laboratory Tests at Least Once Post-dose
NCT02892409 (8) [back to overview]Percentage of Participants Who Meet the Markedly Abnormal Criteria for Vital Sign Measurements at Least Once Post-dose
NCT02978157 (1) [back to overview]Number of Participants in Which H. Pylori Was Eradicated
NCT03050307 (4) [back to overview]Percentage of Helicobacter Pylori Infected (HP+) Participants With Successful HP Eradication After 4 or 8 Weeks of Treatment
NCT03050307 (4) [back to overview]Percentage of Participants With Endoscopically Confirmed Healing of Gastric Ulcers (GUs) at Weeks 4 or 8
NCT03050307 (4) [back to overview]Percentage of Participants With Endoscopically Confirmed Healing of GU at Week 4
NCT03050307 (4) [back to overview]Percentage of Participants With Post-treatment Resolution of Gastrointestinal Symptoms Associated With GU
NCT03050359 (4) [back to overview]Percentage of Participants With Endoscopically Confirmed Healing of Duodenal Ulcers
NCT03050359 (4) [back to overview]Percentage of Participants With Endoscopically Confirmed Healing of Duodenal Ulcer at Week 4
NCT03050359 (4) [back to overview]Percentage of Helicobacter Pylori Infected (HP+) Participants With Successful HP Eradication After 4 or 6 Weeks of Treatment
NCT03050359 (4) [back to overview]Percentage of Participants With Posttreatment Resolution of Gastrointestinal Symptoms Associated With Duodenal Ulcer at Weeks 2 Through 6
NCT04198363 (1) [back to overview]Percentage of Helicobacter Pylori Positive (HP+) Participants With Successful HP Eradication at Week 4 Post-Treatment
NCT04753437 (5) [back to overview]AUCτ: Area Under the Plasma Concentration-time Curve During a Dosing Interval τ for Bismuth
NCT04753437 (5) [back to overview]Cmax: Maximum Observed Plasma Concentration for Bismuth
NCT04753437 (5) [back to overview]Percentage of Participants Who Discontinued Study Drug Due to a Treatment-Emergent Adverse Event (TEAE)
NCT04753437 (5) [back to overview]Percentage of Participants Who Experience at Least One Treatment-Emergent Adverse Event (TEAE)
NCT04753437 (5) [back to overview]Aeτ: Total Amount of Bismuth Excreted in Urine During a Dosing Interval τ for Bismuth
NCT04811339 (3) [back to overview]Day 3 Composite 3 Symptom Score
NCT04811339 (3) [back to overview]Day 3 Composite 5 Symptom Score
NCT04811339 (3) [back to overview]Measure of Daily Stool Frequency for Patients With COVID Treated With Bismuth

Maximum Tolerated Dose

The maximum tolerated dose of bismuth Bi 213 monoclonal antibody M195 following cytarabine in patients with advanced myeloid malignancies. (NCT00014495)
Timeframe: 2 years

InterventionmCi/kg (Number)
Bismuth Bi 213 Monoclonal Antibody M195 & Cytarabine1

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Number of Patients Experiencing Treatment Emergent Adverse Events.

"A treatment-emergent adverse event is defined as an event not present prior to exposure to the study medication or any event already present that worsens in either intensity or frequency following exposure to study medication up to 30 days after study discontinuation.~All safety analysis based on the safety population." (NCT00669955)
Timeframe: at the end of treatment (day 8-14), week 6 and wek 10 follow-up visits.

InterventionParticipants (Number)
Quadruple Therapy (OBMT) 10 Days101
Triple Therapy (OAC) 7 Days112

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H. Pylori Eradication and Presence or Past History of Peptic Ulcers

Eradication rates in the subset of patients with peptic ulcer (current or past history) at baseline are reported based on the per protocol population. Eradication must be confirmed at week 6 and week 10 by a negative Urea Breath Test conducted within the allocated windows. (NCT00669955)
Timeframe: Week 6 and week 10 follow-up visits

InterventionParticipants (Number)
Quadruple Therapy (OBMT) 10 Days18
Triple Therapy (OAC) 7 Days15

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Helicobacter Pylori Eradication Confirmed by Urea Breath Test

H. pylori Eradication defined as a negative C13-UBT (urea breath test) result at both Week 6 and Week 10 follow-up visits. (NCT00669955)
Timeframe: Week 6 and week 10 follow-up visits

InterventionParticipants (Number)
Quadruple Therapy (OBMT) 10 Days166
Triple Therapy (OAC) 7 Days112

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Metronidazole Resistance

Eradication rates in subset of patients infected with a bacterial strain confirmed as resistant to metronidazole at baseline. Resistance to metronidazole defined as Minimum Inhibitory Concentration (MIC) above 8 ug/ml (NCT00669955)
Timeframe: Measured at baseline

Interventionparticipants (Number)
Quadruple Therapy (OBMT) 10 Days38
Triple Therapy (OAC) 7 Days28

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Overall Compliance to Study Medications

Overall compliance: number of capsules dispensed - number of capsules returned/Number of prescribed capsules X 100. Percentages based on safety population (NCT00669955)
Timeframe: At the end of the treatment phase (days 8-14)

Interventionparticipants (Mean)
Quadruple Therapy (OBMT) 10 Days97.58
Triple Therapy (OAC) 7 Days97.47

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Number of Patients With Bismuth Plasma Concentrations Above the Toxic Level

Tolerability of OBMT with respect to plasma bismuth concentrations: number of patients with bismuth concentrations above the toxic level (50 ug per liter) (NCT00669955)
Timeframe: Baseline (both arms), end of treatment (Day 11-14) and end of study (Day 70) OBMT arm only

Interventionparticipants (Number)
Quadruple Therapy (OBMT) 10 Days0

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Clarithromycin Resistance

Eradication rates in subset of patients infected with a bacterial strain confirmed as resistant to clarithromycin at baseline. Resistance to clarithromycin defined as Minimum Inhibitory Concentration (MIC) of 1 ug/ml and above (NCT00669955)
Timeframe: Measured at baseline

Interventionparticipants (Number)
Quadruple Therapy (OBMT) 10 Days30
Triple Therapy (OAC) 7 Days2

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Counts of Participants Whose Drug Compliance is More Than 85%

(NCT02159976)
Timeframe: 4 weeks after termination of eradication therapy, up to 6 weeks

InterventionParticipants (Count of Participants)
Sequential Therapy165
Modified Bismuth Quadruple Therapy170

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Counts of Participants With Adverse Event

(NCT02159976)
Timeframe: 4 weeks after termination of eradication therapy, up to 6 weeks

InterventionParticipants (Count of Participants)
Sequential Therapy93
Modified Bismuth Quadruple Therapy72

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Counts of Participants With Successful H. Pylori Eradication

(NCT02159976)
Timeframe: 4 weeks after termination of eradication therapy, up to 6 weeks

InterventionParticipants (Count of Participants)
Sequential Therapy146
Modified Bismuth Quadruple Therapy134

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Functional Dyspepsia Symptom Responses Rate

(NCT02159976)
Timeframe: 1 year after termination of eradication therapy

,
InterventionParticipants (Count of Participants)
complete (≥75%)Satisfactory (50-74%)Partial (25-49%)Refractory (<25%)
In Eradication Failure Group0012
In Eradication Success Group44169

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Number of Participants in Which H. Pylori Was Eradicated

Repeated endoscopy with rapid urease test, histological examination and culture or urea breath tests are conducted to assess H. pylori status. (NCT02541864)
Timeframe: at the 6th week after the end of anti- H. pylori therapy

Interventionparticipants (Number)
Pantoprazole+Bismuth+Tetra+Metro154
Hybrid Therapy154

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Number of Participants in Which H. Pylori Was Eradicated

Evaluate eradication outcome by endoscopy urease test and histology or urea breath test (Number of Participants With Complete Eradication of Helicobacter Pylori) (NCT02547038)
Timeframe: sixth week after the end of anti- H. pylori therapy

Interventionparticipants (Number)
Pantoprazole+Bismuth+Tetra+Metro169
(Panto+Amox+Clar+Metr)+(Panto+Amox)170

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Number of Excess Double-strand DNA Break Foci Per Cell in Peripheral Blood Samples Post-imaging

The amount of excess DNA double-strand break foci per cell after cardiac computed tomographic angiography (CCTA) in female patients with and without breast shields, minus the amount of foci prior to CCTA. In addition, changes in DNA double-strand breaks from baseline following cardiac testing in the observational arm is being assessed in an observational manner. (NCT02617888)
Timeframe: Change from baseline double strand DNA breaks at 30 minutes post-imaging

Interventiongamma-H2AX foci in blood lymphocytes (Mean)
No Breast Shields0.183
Breast Shields0.159

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Aeτ: Amount of Drug Excreted in Urine During a Dosing Interval for Bismuth

(NCT02892409)
Timeframe: Day 14 pre-dose and at multiple timepoints (up to 12 hours) post-dose

Interventionnanogram (ng) (Mean)
Clarithromycin + Amoxicillin + Bismuth + TAK-438497300
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole537600

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AUCτ: Area Under the Plasma Concentration-time Curve From Time 0 to Time Tau Over the Dosing Interval for Bismuth

(NCT02892409)
Timeframe: Day 14 pre-dose and at multiple timepoints (up to 12 hours) post-dose

Interventionhours nanogram per milliliter (h*ng/mL) (Mean)
Clarithromycin + Amoxicillin + Bismuth + TAK-438103.0
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole111.1

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Cmax: Maximum Observed Plasma Concentration for Bismuth

(NCT02892409)
Timeframe: Day 14 pre-dose and at multiple timepoints (up to 12 hours) post-dose

Interventionnanogram per milliliter (ng/mL) (Mean)
Clarithromycin + Amoxicillin + Bismuth + TAK-43828.08
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole30.14

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Percentage of Participants Who Discontinue Due to an Adverse Event (AE)

(NCT02892409)
Timeframe: Baseline up to Day 17

Interventionpercentage of participants (Number)
Clarithromycin + Amoxicillin + Bismuth + TAK-4386.7
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole0.0

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Percentage of Participants Who Experience at Least One Treatment Emergent Adverse Event (TEAE)

(NCT02892409)
Timeframe: Baseline up to Day 17

Interventionpercentage of participants (Number)
Clarithromycin + Amoxicillin + Bismuth + TAK-43853.3
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole66.7

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Percentage of Participants Who Meet the Markedly Abnormal Criteria for Safety Electrocardiogram (ECG) Parameters at Least Once Post-dose

(NCT02892409)
Timeframe: Baseline up to Day 15

Interventionpercentage of participants (Number)
Clarithromycin + Amoxicillin + Bismuth + TAK-4380.0
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole6.7

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Percentage of Participants Who Meet the Markedly Abnormal Criteria for Safety Laboratory Tests at Least Once Post-dose

(NCT02892409)
Timeframe: Baseline up Day 15

,
Interventionpercentage of participants (Number)
Amylase (greater than [>] 2*upper limit of normal)Potassium (>6.0 millimole per liter [mmol/L])
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole6.76.7
Clarithromycin + Amoxicillin + Bismuth + TAK-4380.00.0

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Percentage of Participants Who Meet the Markedly Abnormal Criteria for Vital Sign Measurements at Least Once Post-dose

(NCT02892409)
Timeframe: Baseline up to Day 15

,
Interventionpercentage of participants (Number)
Body temperature (less than [<] 35.6 celsius [C])Body temperature (>37.7 C)Systolic blood pressure(<85 millimeter of mercury)Diastolic blood pressure(<50millimeter of mercury)
Clarithromycin + Amoxicillin + Bismuth + Lansoprazole6.76.76.76.7
Clarithromycin + Amoxicillin + Bismuth + TAK-4380.06.76.76.7

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Number of Participants in Which H. Pylori Was Eradicated

Number of participants with negative H pylori status in follow-up tests as a measure of successful eradication (NCT02978157)
Timeframe: six weeks after the end of anti-H pylori therapy.

Interventionparticipants (Number)
Esomeprazole+Amox+Levo36
Esomeprazole+Bismuth+Tetra+Levo49

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Percentage of Helicobacter Pylori Infected (HP+) Participants With Successful HP Eradication After 4 or 8 Weeks of Treatment

HP infection status was determined by 13C-UBT. The urea breath test is used to detect infection with HP, a bacteria associated with stomach ulcers, by testing individual breath samples in a central laboratory. The data is provided only for HP+ participants. The participant could take 4 or 8 weeks of treatment for GU healing, then additional 4 weeks later, to have the urea breath test (UBT) test to detect HP. (NCT03050307)
Timeframe: 4 weeks post treatment (up to approximately 12 weeks)

Interventionpercentage of participants (Number)
TAK-438 20 mg88.0
Lansoprazole 30 mg80.8

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Percentage of Participants With Endoscopically Confirmed Healing of Gastric Ulcers (GUs) at Weeks 4 or 8

Endoscopic healing was defined as the disappearance of all white coats associated with GUs confirmed endoscopically. (NCT03050307)
Timeframe: Week 4 or 8

Interventionpercentage of participants (Number)
TAK-438 20 mg91.1
Lansoprazole 30 mg94.7

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Percentage of Participants With Endoscopically Confirmed Healing of GU at Week 4

Endoscopic healing was defined as the disappearance of all white coats associated with GUs confirmed endoscopically. (NCT03050307)
Timeframe: Week 4

Interventionpercentage of participants (Number)
TAK-438 20 mg76.1
Lansoprazole 30 mg82.1

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Percentage of Participants With Post-treatment Resolution of Gastrointestinal Symptoms Associated With GU

The gastrointestinal symptoms included epigastric pain [postprandial, fasting, nocturnal], abdominal bloating, nausea/vomiting, heartburn, lack of appetite. The severity of gastrointestinal symptoms associated with GU were recorded as: none = 0, mild = 1, moderate = 2 or severe = 3. The data is reported in categories for percentage of participants with resolution of gastrointestinal symptoms associated with GU. (NCT03050307)
Timeframe: Week 2 up to Week 8

,
Interventionpercentage of participants (Number)
Epigastric Pain (Postprandial)Epigastric Pain (Fasting/Nocturnal)Abdominal BloatingNausea/VomitingHeartburnLack of Appetite
Lansoprazole 30 mg80.080.565.2100.085.790.0
TAK-438 20 mg78.985.081.3100.095.877.8

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Percentage of Participants With Endoscopically Confirmed Healing of Duodenal Ulcers

Endoscopic healing was defined as the disappearance of all white coats associated with duodenal ulcers as confirmed endoscopically. (NCT03050359)
Timeframe: Week 4 or Week 6

Interventionpercentage of participants (Number)
TAK-438 20 mg96.9
Lansoprazole 30 mg96.5

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Percentage of Participants With Endoscopically Confirmed Healing of Duodenal Ulcer at Week 4

Endoscopic healing is defined as the disappearance of all white coats associated with duodenal ulcers as confirmed endoscopically. (NCT03050359)
Timeframe: Week 4

Interventionpercentage of participants (Number)
TAK-438 20 mg89.2
Lansoprazole 30 mg88.4

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Percentage of Helicobacter Pylori Infected (HP+) Participants With Successful HP Eradication After 4 or 6 Weeks of Treatment

HP infection status was determined by ^13C Urea Breath Test (^13C-UBT). The urea breath test is used to detect infection with HP, a bacteria associated with stomach ulcers, by testing individual breath samples in a central laboratory. (NCT03050359)
Timeframe: 4 weeks post treatment (Up to 10 weeks)

Interventionpercentage of participants (Number)
TAK-438 20 mg91.5
Lansoprazole 30 mg86.8

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Percentage of Participants With Posttreatment Resolution of Gastrointestinal Symptoms Associated With Duodenal Ulcer at Weeks 2 Through 6

The percentage of participants with resolution of various gastrointestinal symptoms are reported as categories. Gastrointestinal symptoms included epigastric pain (postprandial, fasting, nocturnal), abdominal bloating, nausea/vomiting, heartburn and lack of appetite. The severity of subjective symptoms of erosive esophagitis were recorded as: none = 0, mild = 1, moderate = 2 or severe = 3. (NCT03050359)
Timeframe: Week 2 up to Week 6

,
Interventionpercentage of participants (Number)
Epigastric Pain (Postprandial)Epigastric Pain (Fasting/Nocturnal)Abdominal BloatingNausea/VomitingHeartburnLack of Appetite
Lansoprazole 30 mg91.890.187.394.495.5100.0
TAK-438 20 mg87.791.783.385.2100.090.9

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Percentage of Helicobacter Pylori Positive (HP+) Participants With Successful HP Eradication at Week 4 Post-Treatment

HP infection status was determined by ^13C Urea Breath Test (^13C-UBT). The urea breath test is used to detect infection with HP, a bacteria associated with stomach ulcers, by testing individual breath samples in a central laboratory. The percentages are rounded off to report the nearest ten. (NCT04198363)
Timeframe: Week 4 post-treatment

Interventionpercentage of participants (Number)
Vonoprazan 20 mg86.8
Esomeprazole 20 mg86.7

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AUCτ: Area Under the Plasma Concentration-time Curve During a Dosing Interval τ for Bismuth

(NCT04753437)
Timeframe: Day 14: 0 to 12 hours after the morning dose

Interventionhour*nanogram/milliliter (h*ng/mL) (Geometric Least Squares Mean)
Clarithromycin + Amoxicillin + Bismuth + Vonoprazan146
Clarithromycin + Amoxicillin + Bismuth + Esomeprazole137

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Cmax: Maximum Observed Plasma Concentration for Bismuth

(NCT04753437)
Timeframe: Day 14: 0 to 12 hours after the morning dose

Interventionnanogram per milliliter (ng/mL) (Geometric Least Squares Mean)
Clarithromycin + Amoxicillin + Bismuth + Vonoprazan42.8
Clarithromycin + Amoxicillin + Bismuth + Esomeprazole32.9

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Percentage of Participants Who Discontinued Study Drug Due to a Treatment-Emergent Adverse Event (TEAE)

(NCT04753437)
Timeframe: From the first dose of study drug up to Day 17

Interventionpercentage of participants (Number)
Clarithromycin + Amoxicillin + Bismuth + Vonoprazan9.1
Clarithromycin + Amoxicillin + Bismuth + Esomeprazole22.7

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Percentage of Participants Who Experience at Least One Treatment-Emergent Adverse Event (TEAE)

An adverse event (AE) is defined as any untoward medical occurrence in a clinical investigation participant administered a drug; it does not necessarily have to have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (e.g., a clinically significant abnormal laboratory finding), symptom, or disease temporally associated with the use of a drug, whether or not it is considered related to the drug. A TEAE is defined as an AE with an onset that occurs after receiving study drug. (NCT04753437)
Timeframe: From the first dose of study drug up to Day 17

Interventionpercentage of participants (Number)
Clarithromycin + Amoxicillin + Bismuth + Vonoprazan95.5
Clarithromycin + Amoxicillin + Bismuth + Esomeprazole95.5

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Aeτ: Total Amount of Bismuth Excreted in Urine During a Dosing Interval τ for Bismuth

(NCT04753437)
Timeframe: Day 14: 0 to 12 hours after the morning dose

Interventionmicrograms (μg) (Mean)
Clarithromycin + Amoxicillin + Bismuth + Vonoprazan1026
Clarithromycin + Amoxicillin + Bismuth + Esomeprazole1037

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Day 3 Composite 3 Symptom Score

The 3 symptom composite score was generated from 3 symptoms: Cough, Headache, and Fatigue. Each symptom was scored as such: 0 was not affected, 1 was little affected, 2 moderately affected, 3 severely affected. A composite score was generated using the score given for each individual symptom, ie. the sum of symptomatic score of Cough + symptomatic score of Headache + symptomatic score of Fatigue. The maximum and most symptomatic composite score could be 9 each day. The minimum score could be 0 . This score was calculated calculated for BL/day1, day 2 and day 3 . This outcome is the composite 3 symptom score on day 3. (NCT04811339)
Timeframe: This is the day 3 composite score

Interventionscore on a scale (Mean)
Open Label BSS Therapy -Completed1.4

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Day 3 Composite 5 Symptom Score

The 5 symptom composite score was generated from 5 symptoms: Cough, Headache, Fatigue, Shortness of Breath, and Anosmia (no smell). Each symptom was scored as such: 0 was not affected, 1 was little affected, 2 moderately affected, 3 severely affected. A composite score was generated using the score given for each individual symptom, ie. the sum of symptomatic score of Cough + symptomatic score of Headache + symptomatic score of Fatigue + symptomatic score of Shortness of Breath + symptomatic score of anosmia. The maximum and most symptomatic composite score could be 15 each day. The minimum score could be 0. This score was calculated calculated for BL/day1, day 2 and day 3 . This outcome is the composite 5 symptom score on day 3. (NCT04811339)
Timeframe: The score was taken at BL (baseline)/day 1, Day 2 ( 24 hours after BSS started ) and Day 3 (48 hours after BSS started). This Outcome is Day 3 score.

Interventionscore on a scale (Mean)
Open Label BSS Therapy -Completed2.9

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Measure of Daily Stool Frequency for Patients With COVID Treated With Bismuth

Number of bowel movements recorded over the 3 day study. Baseline (BL) /day1 + Day 2 + Day 3 (NCT04811339)
Timeframe: 3 days

Interventionbowel movements (Mean)
Open Label BSS Completed Patients3

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