drugset / Trial / NCT00252720

DIabetic Retinopathy Candesartan Trials.

NCT00252720 ↗

Phase 3 Completed 1850 enrolled AstraZeneca Takeda · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective is to determine whether candesartan, compared to placebo reduces the progression of diabetic retinopathy in normotensive, normoalbuminuric type 1 diabetic patients with retinopathy. The secondary objective is to determine whether candesartan, compared to placebo, reduces the incidence of clinically significant macular oedema (CSME) and/or proliferative diabetic retinopathy (PDR) and beneficially influences the rate of change in urinary albumin excretion rate (UAER). This study is part of the DIRECT Programme also including a primary prevention study of diabetic retinopathy in type 1 diabetes and a secondary prevention study in 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
2001-08
Primary completion
2008-02
Completion
2008-04

Outcome

Missed primary endpoint

registry Candesartan vs Placebo; p = 0.8487; Hazard Ratio (HR) 1.024 (95% CI 0.800 to 1.312); Log Rank NCT00252720 ↗

paper Progression of retinopathy occurred in 127 (13%) participants in the candesartan group versus 124 (13%) in the placebo group. PMID 18823656 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Candesartan Unknown 32 mg Oral