Newer Versus Older Antihypertensive Agents in African Hypertensive Patients (NOAAH) Trial
NCT01030458 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 183
Last updated 2013-12-09
Summary
The purpose of this study is to compare the blood pressure lowering efficacy of a treatment regimen based on a dihydropyridine calcium-channel blocker combined with an angiotensin II type-1 receptor blocker with the recommended treatment regimen based on a low-dose thiazide diuretic combined with a beta-blocker.
Conditions
- Blood Pressure
Interventions
- DRUG
-
amlodipine 5/10 mg per day plus valsartan 160 mg/day
Amlodipine 5/10 mg/day plus valsartan 160 mg/day, once daily, in the morning
- DRUG
-
hydrochlorothiazide 6.25 mg/day plus bisoprolol 5/10 mg/day
hydrochlorothiazide 6.25 mg/day plus bisoprolol 5/10 mg/day, once daily, in the morning
Sponsors & Collaborators
-
University of Kinshasa
collaborator OTHER -
Yaounde Central Hospital
collaborator OTHER_GOV -
University of Yaounde
collaborator OTHER -
University of Libreville
collaborator UNKNOWN -
Institute of Cardiology Abidjan
collaborator UNKNOWN -
University of Ilorin Teaching Hospital
collaborator OTHER -
University of Nigeria, Enugu Campus
collaborator OTHER -
Hospital Aristide Le Dantec, Dakar, Senegal
collaborator UNKNOWN -
KU Leuven
lead OTHER
Principal Investigators
-
Samuel Kingue, MD · Hôpital Général de Yaoundé, BP 5408, Yaoundé, Cameroun
-
Daniel Lemogoum, MD, PhD · Université de Douala, Douala, Cameroon
-
Bruno Mipinda, MD · Hôpital Central Universitaire de Libreville, Libreville, Gabon
-
Omotoso Babatunde, MD · University of Ilorin, Ilorin, Nigeria
-
Ifeoma E Ulasi, MD · University of Enugu, Enugu, Nigeria
-
Serigne Abdou Ba, MD · Hôpital Aristide Le Dantec, Dakar, Sénégal
-
Jean-René M'Buyamba-Kabangu, MD, PhD · University of Kinshasa, Kinshasa, Democratic Republic of Congo
-
Jan A Staessen, MD, PhD · University of Leuven, Leuven, Belgium
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 30 Years
- Max Age
- 69 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-09-30
- Primary Completion
- 2012-03-31
- Completion
- 2012-03-31
Countries
- Cameroon
- Côte d’Ivoire
- Gabon
- Nigeria
- Senegal
Study Locations
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