Clinical Trials Directory

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

TypeNameDescription
DRUGramipril
DRUGramipril-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.

Higher Dose of Ramipril Versus Addition of Telmisartan-Ramipril in Hypertension and Diabetes (NCT00208221) · Clinical Trials Directory