Clinical Trials Directory

Trials / Completed

CompletedNCT04254042

Comparative Effects of Perindopril and Zofenopril on Blood Pressure Control and Oxidative Status Blacks Hypertensive Patients.

Rationale and Design of a Simple Randomized Trial Evaluating Comparative Effects of Perindopril and Zofenopril in Blacks Hypertensive Patients: Short Term Effects on Cardiac and Oxidative Status With Perindopril or Zofenopril (PEZO-HP) Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Yaounde Central Hospital · Other Government
Sex
All
Age
21 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to compare the short term effect of perindopril and zofenopril in the management of hypertension and the oxydative stress in blacks hypertensive patients. PEZO-HP is a double-arm, double-blind, randomized and parallel clinical trial conducted at the Yaoundé Central Hospital.

Detailed description

Aim: to determine and compare the short term effect of angiotensin converting in the management of hypertension as well as the oxidative effect of Zofenopril and perindopril in blacks hypertensive patients in the Yaoundé Central Hospital. Method: A double-arm, double-blind, randomized and parallel clinical trial conducted at the Yaoundé Central Hospital. Hypertensive patients who are not taking angiotensin-converting enzyme inhibitor or angiotensin receptors blockers, are randomize into 2 groups. Depending on the group, the intervention consisted of the administration of Perindopril 10 mg daily or Zofenopril 30 mg daily for 08 weeks. The endpoints were the nycthemeral blood pressure profile, pro oxidant marker (malondialdehyde) and anti-oxidant marker (Ferric reducing antioxidant). Progress: Recruitment for PEZO-HP was completed in May 2019 with 24 patients.

Conditions

Interventions

TypeNameDescription
DRUGPerindopril Arginine10 mg Perindopril tablet / day will be added to the usual treatment for each patient for a period of 8 weeks.
DRUGZofenopril, Calcium Salt, (1(R*),2Alpha,4Alpha)-isomer30 mg Zofenopril tablet / day will be added to the usual treatment for each patient for a period of 8 weeks.

Timeline

Start date
2018-10-01
Primary completion
2019-05-01
Completion
2019-05-01
First posted
2020-02-05
Last updated
2020-02-05

Locations

1 site across 1 country: Cameroon

Source: ClinicalTrials.gov record NCT04254042. Inclusion in this directory is not an endorsement.