Trial | NCT02742467  Report issue

Official Title

Comparison of Three Combination Therapies in Lowering Blood Pressure in Black Africans

  • Phase

    Phase 4

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    702
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.
Study Started
Jun 07
2017
Primary Completion
Jun 01
2018
Study Completion
Jun 01
2018
Last Update
Aug 24
2021

Drug Perindopril plus Hydrochlorothiazide

Group 2

Drug Amlodipine plus Hydrochlorothiazide

Group 3

Drug Perindopril plus Amlodipine

Group 1

1 Experimental

Perindopril plus Amlodipine at a dose of 4mg/5mg once daily for two months and 8mg/10mg once daily for the remaining four months.

2 Active Comparator

Perindopril Plus Hydrochlorothiazide at a dose of 4mg/12.5mg and 8mg/25mg once daily for the remaining four months.

3 Active Comparator

Amlodipine plus Hydrochlorothiazide 5mg/12.5mg for two months and 10mg/25mg for the remaining four months.

Criteria 

Inclusion Criteria:

Patients with Sitting SBP ≥140 mm Hg and < 160 mmHg on one antihypertensive agen or
Sitting SBP ≥ 150 mm Hg and < 180 mm Hg on no antihypertensive treatment.

Exclusion Criteria:

Congestive heart failure (clinically defined).
Serum creatinine levels greater than 170 µmol/l or estimated glomerular filtration rate (eGFR) < 30 ml/min.
History of coronary heart disease (i.e., chronic stable angina, myocardial infarction or acute coronary syndrome).
History of a stroke or other cerebrovascular accident (i.e. transient ischaemic attack or reversible ischaemic neurological deficit).
Known or suspected secondary hypertension.
Any other concomitant illness, physical or mental impairment that could interfere with the effective conduct of the study.
Pregnancy or those of child-bearing age who are not taking reliable contraception.
Patients with a history of intolerance to any of the study medications for example angioedema or dry cough with angiotensin converting enzyme inhibitors.
Patients on maximum dose of any of the study medications as monotherapy (i.e. amlodipine 10 mg/day or hydrochlorothiazide 25 mg/day or perindopril 8 mg/day)
Gout.
Serum potassium < 3.5mmol/L at screening.
No Results Posted