Page last updated: 2024-10-22

amlodipine and Alport Syndrome

amlodipine has been researched along with Alport Syndrome in 2 studies

Amlodipine: A long-acting dihydropyridine calcium channel blocker. It is effective in the treatment of ANGINA PECTORIS and HYPERTENSION.
amlodipine : A fully substituted dialkyl 1,4-dihydropyridine-3,5-dicarboxylate derivative, which is used for the treatment of hypertension, chronic stable angina and confirmed or suspected vasospastic angina.

Research Excerpts

ExcerptRelevanceReference
"Twelve weeks of treatment with losartan significantly reduced proteinuria compared with placebo/amlodipine: losartan -14."9.15Efficacy and safety of losartan in children with Alport syndrome--results from a subgroup analysis of a prospective, randomized, placebo- or amlodipine-controlled trial. ( Gleim, GW; Lam, C; Le Bailly De Tilleghem, C; Shahinfar, S; Strehlau, J; Webb, NJ; Wells, TG, 2011)
"Twelve weeks of treatment with losartan significantly reduced proteinuria compared with placebo/amlodipine: losartan -14."5.15Efficacy and safety of losartan in children with Alport syndrome--results from a subgroup analysis of a prospective, randomized, placebo- or amlodipine-controlled trial. ( Gleim, GW; Lam, C; Le Bailly De Tilleghem, C; Shahinfar, S; Strehlau, J; Webb, NJ; Wells, TG, 2011)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Webb, NJ1
Lam, C1
Shahinfar, S1
Strehlau, J1
Wells, TG1
Gleim, GW1
Le Bailly De Tilleghem, C1
Canpolat, U1
Aytemir, K1
Tokgözoğlu, L1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized, Double-Blind, Parallel, Placebo or Amlodipine-Controlled Study of the Effects of Losartan on Proteinuria in Pediatric Patients With or Without Hypertension[NCT00568178]Phase 3306 participants (Actual)Interventional2007-06-01Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Double-Blind Treatment Phase: Change From Baseline in Diastolic Blood Pressure in Hypertensive Participants at Week 12

(NCT00568178)
Timeframe: Baseline and Week 12

Interventionmm Hg (Least Squares Mean)
Losartan-Hypertensive Participants-3.8
Amlodipine-Hypertensive Participants0.8

Double-Blind Treatment Phase: Change From Baseline in Systolic Blood Pressure in Hypertensive Participants at Week 12

(NCT00568178)
Timeframe: Baseline and Week 12

Interventionmm Hg (Least Squares Mean)
Losartan-Hypertensive Participants-5.5
Amlodipine-Hypertensive Participants-0.1

Double-Blind Treatment Phase: Percent Change From Baseline in Urinary Protein/Creatinine (Pr/Cr) Ratio (gm/gm) at Week 12

"Change in urinary protein excretion, determined as urinary Pr/Cr ratio compared to baseline*, after approximately twelve weeks of treatment.~Baseline is defined as values obtained at Visit 3, Week (-1) during the Single Blind Run-in period." (NCT00568178)
Timeframe: Baseline and Week 12

InterventionPercent Change in Pr/Cr (Geometric Mean)
Losartan-35.80
Amlodipine/Placebo1.37

Open Label Extension: Change From Baseline in Glomerular Filtration Rate (GFR) at Month 36

"The outcome measure of glomerular filtration rate was based on mL/min/1.73m^2, as determined by the Schwartz formula:~GFR = _____0.55 x height (cm)_______ divided by serum creatinine (mg/dL)~GFR values were compared to the baseline GFR measure.~[Note: For male participants, ages 13 to 17 years, 0.70 was used as~the multiplier in place of 0.55]~Baseline in regard to the extension is defined as the last value obtained in the double-blind treatment phase." (NCT00568178)
Timeframe: Baseline and Month 36

InterventionChange in GFR mL/min1.73m^2 (Least Squares Mean)
Losartan Open Label Extension3.3
Enalapril Open Label Extension7.0

Open Label Extension: Percent Change From Baseline of Urinary Pr/Cr Ratio (gm/gm) at Month 36

"Change in urinary protein excretion, determined as urinary Pr/Cr ratio compared to baseline*, after approximately three years of treatment.~*The baseline for efficacy data in the extension was defined as the last value obtained in the double-blind treatment phase." (NCT00568178)
Timeframe: Baseline and Month 36

InterventionPercent Change in Pr/Cr (Geometric Mean)
Losartan Open Label Extension-30.01
Enalapril Open Label Extension-40.45

Trials

1 trial available for amlodipine and Alport Syndrome

ArticleYear
Efficacy and safety of losartan in children with Alport syndrome--results from a subgroup analysis of a prospective, randomized, placebo- or amlodipine-controlled trial.
    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2011, Volume: 26, Issue:8

    Topics: Adolescent; Adult; Amlodipine; Antihypertensive Agents; Blood Pressure; Child; Child, Preschool; Dou

2011

Other Studies

1 other study available for amlodipine and Alport Syndrome

ArticleYear
Two-in-one: single coronary ostium and mitral valve prolapsus in a young female with Alport syndrome.
    Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology, 2012, Volume: 12, Issue:3

    Topics: Amlodipine; Antihypertensive Agents; Autoantigens; Carbazoles; Carvedilol; Collagen Type IV; Coronar

2012