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The creole study is a A Multi-centre, multinational, randomised single-blind, parallel group, three-armed superiority trial which is aimed at comparing the efficacy of three "free" combinations of two anti-hypertensive agents on 24 hour ambulatory systolic blood pressure (ASBP) in black African hypertensive patients.
The CREOLE trial will be performed at ten investigational sites in six countries in Sub-Saharan Africa which include Cameroun, Kenya, Mozambique, Nigeria, South Africa and Uganda. Subjects will be randomised to one of three treatments which are Perindopril plus Amlodipine or Perindopril plus Hydrochlorothiazide or Amlodipine plus Hydrochlorothiazide.Patients will commence treatment at a starting dose of Amlodipine plus Hydrochlorothiazide 5/12.5 mg or Amlodipine plus Perindopril 5/4 mg or Perindopril/Hydrochlorothiazide 4/12.5 mg. These doses will increase at the two months visit, to Amlodipine/Hydrochlorothiazide 10/25 mg or AmlodipinePperindopril 10/8mg or Perindopril/Hydrochlorothiazide 8/25 mg. The patients will have ambulatory blood pressure monitoring at randomization and at six months and office blood pressure measurements at randomization and at two-month, 4-month and six-month visits.The overall aim is to discover the best combination of front-line anti-hypertensive medications for black patients residing in sub-Saharan Africa.
Age
30 - 79 years
Sex
ALL
Healthy Volunteers
No
University of Abuja Teaching Hospital
Abuja, Federal Capital Territory, Nigeria
Start Date
June 7, 2017
Primary Completion Date
June 1, 2018
Completion Date
June 1, 2018
Last Updated
August 24, 2021
702
ACTUAL participants
Perindopril plus Amlodipine
DRUG
Perindopril plus Hydrochlorothiazide
DRUG
Amlodipine plus Hydrochlorothiazide
DRUG
Lead Sponsor
University of Abuja
Collaborators
Data Source & Attribution
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