Trials / Terminated
TerminatedNCT00208221
Higher Dose of Ramipril Versus Addition of Telmisartan-Ramipril in Hypertension and Diabetes
Comparison of a Higher Dose of Ramipril to the Addition of Telmisartan 80 mg+Ramipril 10 mg in Patients With Hypertension and Diabetes
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Institut de Recherches Cliniques de Montreal · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine if a dose of ramipril combined with a normal dose of telmisartan 80 mg will be more effective than ramipril 20 mg in reducing microalbuminuria in hypertensive patients with diabetes.
Detailed description
The purpose of this study is to determine the effects of ramipril 10 mg and telmisartan 80 mg versus ramipril 20 mg in patients with diabetes type II, hypertension and microalbuminuria (Urinary-albuminuria creatinine ratio of 2.0 to 25 mg/mmol) on 1. Microalbuminuria 2. Blood pressure (systolic, diastolic and ABPM), Renin-angiotensin system, Catecholamines, Oxydative stress 3. Comparison at 4, 8 and 12 weeks with addition of hydrochlorothiazide 12.5 mg if BP over 130/80 mmHg
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | ramipril | |
| DRUG | ramipril-telmisartan |
Timeline
- Start date
- 2006-08-01
- Completion
- 2007-06-01
- First posted
- 2005-09-21
- Last updated
- 2007-11-08
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT00208221. Inclusion in this directory is not an endorsement.