CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 560 enrolled
Drug / intervention
ACEI/CCB +1 moredrug
Likely dose
ACEI/CCB 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03682692
NCT03682692Phase 4Completed

ACEI/CCB Versus ACEI/DIU Combination Antihypertensive Therapy in Chinese Hypertensive Patients (ACvAD)

Shanghai Jiao Tong University School of Medicine·interventional·Posted Sep 25, 2018·Updated Feb 14, 2023

In Brief

A Phase 4 clinical trial evaluating ACEI/CCB and ACEI/DIU for Hypertension. Completed, enrolled 560 participants across 1 site.

Detailed Summary

1. Study name: ACEI/CCB versus ACEI/DIU combination antihypertensive therapy in Chinese hypertensive patients (ACvAD) 2. Rationale:Most current hypertension guidelines recommend the combination therapy of an angiotensin-converting enzyme inhibitors (ACEI) or angiotensin receptor blockers (ARB) with a calcium antagonists (CCB) or thiazide diuretics (DIU). However, whether the two combination treatments have similar antihypertensive effects in Chinese hypertensive patients is still lack of clinical evidence, especially randomized controlled trials using ambulatory or home blood pressure measurement as the main evaluation method. 3. Study design: This study is a multi-center, randomized and controlled clinical trial with two equally sized treatment groups: ACEI/CCB group and ACEI/DIU group. 4. Study population: Men or women over 18 years (n=580) meeting the inclusion/exclusion criteria. 5. Randomization and treatment: Potentially eligible patients should receive a 24-hour ambulatory blood pressure monitoring measurement before randomization. After stratification by centers and whether receive antihypertensive treatment, eligible patients will be randomly divided into two groups, taking benazepril 10 mg/amlodipine besylate 5mg fixed-dose combination (1 tablet once a day) or benazepril 10 mg/hydrochlorothiazide 12.5 mg fixed-dose combination (1 tablet once a day). 6. Follow up: All patients should sign an informed consent form before entering the study. The follow-up period is 6 months. 7. Sample size estimation: a total of 580 patients should be enrolled in this study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHypertension
CountriesChina
Collaborators--

Timeline

Phase 4CompletedFinished
20192020202120222023202420252026
First PostedSep 25, 2018
Enrollment StartJun 1, 2018
Primary CompletionJun 30, 2021
Study CompletionMar 31, 2022
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 7.8 years ago

Interventions

ACEI/CCBdrug

benazepril 10 mg / amlodipine besylate 5 mg fixed-dose combination

ACEI/DIUdrug

benazepril 10 mg / hydrochlorothiazide 12.5 mg fixed-dose combination