Trials / Completed
CompletedNCT00367094
Combination of Benazepril Plus Hydrochlorothiazide in Chinese Patients With Mild to Moderate Essential Hypertension
Efficacy and Safety of the Combination of Benazepril Plus Hydrochlorothiazide in Chinese Patients With Mild to Moderate Essential Hypertension Not Adequately Controlled With Benazepril
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 296 (planned)
- Sponsor
- Novartis · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate efficacy and safety data for benazepril/hydrochlorothiazide in adult Chinese patients with mild to moderate essential hypertension. Patients whose blood pressure is not adequately controlled with benazepril monotherapy during a 4 week run-in period will be randomly allocated to double blind treatment over 8 weeks with either a combination of benazepril/hydrochlorothiazide per day or continuation of benazepril per day.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Benazepril plus hydrochlorothiazide |
Timeline
- Start date
- 2006-07-01
- First posted
- 2006-08-22
- Last updated
- 2007-07-09
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT00367094. Inclusion in this directory is not an endorsement.