Clinical Trials Directory

Trials / Completed

CompletedNCT03393715

Effect of Morning Versus Evening Perindopril on Blood Pressure Control in People With Type 2 Diabetes

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Yaounde Central Hospital · Other Government
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

We assessed the influence of time of administration of ACE inhibitors on circadian blood pressure control in sub Saharan type 2 diabetes patients with stage 1 hypertension over 56 days as first line treatment.

Detailed description

Background: Renin-angiotensin system antagonists represent the mainstay of blood pressure (BP) lowering treatment options in people with diabetes. ACE inhibitors have a long half-life and offer the advantage of a single daily dose, usually empirically taken in the morning. Objective: We assessed the influence of time of administration of ACE inhibitors on circadian BP control in type 2 diabetes (T2D) patients with stage 1 hypertension. Methods: Twenty T2D patients (9 being women) with a mean age of 58.7 years, diagnosed with stage 1 of hypertension and naive to BP lowering medications, were included. They were randomly allocated to receive perindopril 10 mg/day as a monotherapy either in the morning or in the evening for 28 days, with crossover without washout period on day 29th and additional 28 days follow-up. A 24-hour ambulatory BP monitoring (ABPM) was performed at baseline, days 28 and 56.

Conditions

Interventions

TypeNameDescription
DRUGPerindopril Oral TabletPerindopril oral tablet morning versus evening

Timeline

Start date
2016-02-01
Primary completion
2016-07-01
Completion
2016-08-01
First posted
2018-01-08
Last updated
2018-01-08

Source: ClinicalTrials.gov record NCT03393715. Inclusion in this directory is not an endorsement.