drugset / Trial / NCT00252733

Diabetic Retinopathy Candesartan Trials

NCT00252733

Phase 3 Completed 5238 enrolled AstraZeneca Takeda · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective is to determine whether candesartan, compared to placebo reduces the incidence of diabetic retinopathy in normotensive, normoalbuminuric type 1 diabetic patients without retinopathy. The secondary objective is to determine whether candesartan, compared to placebo, beneficially influences the rate of change in urinary albumin excretion rate (UAER). This study is part of the DIRECT Programme also including secondary prevention studies of diabetic retinopathy in both type 1 and type 2 diabetes. The primary objective for all three pooled studies is to determine whether candesartan, compared to placebo, reduces the incidence of microalbuminuria in type 1 and type 2 diabetic patients.

Timeline

Start
2001-06
Primary completion
2008-04
Completion
2008-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Candesartan Unknown 32 mg Oral