Hypertension Clinical Trial
Official title:
The Irbesartan in Patients With Type 2 Diabetes and Microalbuminuria (IRMA 2)
NCT number | NCT00317915 |
Other study ID # | EFC2481 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | April 24, 2006 |
Last updated | April 24, 2006 |
Verified date | April 2006 |
Source | Steno Diabetes Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | Denmark: Danish Medicines Agency |
Study type | Interventional |
The aim of this multicenter, doubleblind, randomized study was to investigate the renoprotective effect of irbesartan treatment in patients with type 2 diabetes and microalbuminuria (a precursor of diabetic kidney disease). 590 patients were randomized to a median 24 months of treatment with 300 mg irbesartan once daily, 150 mg irbesartan once daily or placebo. Time to development of overt nephropathy, defined by persistent proteinuria, was the primary outcome measure.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 30 Years to 70 Years |
Eligibility |
Inclusion Criteria: Type 2 diabetes. Hypertension. Persistent microalbuminuria. Serum creatinine concentration of no more than 1.5 mg per deciliter (133 µmol per liter) for men and no more than 1.1 mg per deciliter (97 µmol per liter) for women. - Exclusion Criteria: Nondiabetic kidney disease. Cancer. Life-threatening disease with death expected to occur within two years. Indication for angiotensin-converting– enzyme (ACE) inhibitors or angiotensin-II–receptor antagonists. - |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Steno Diabetes Center | Bristol-Myers Squibb, Sanofi-Synthelabo |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Development of overt nephropathy |
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
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