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

Study results available
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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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01030458 on ClinicalTrials.gov