drugset / Trial / NCT00120003

Scandinavian Candesartan Acute Stroke Trial (SCAST)

NCT00120003 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to assess whether the blood pressure lowering agent candesartan (an angiotensin receptor type 1 blocker) is effective when given to patients with acute stroke and elevated blood pressure. Hypothesis: AT1 receptor blockade with candesartan in acute stroke will: 1. reduce the risk of death or major disability at 6 months by a 6% absolute risk reduction, relative to placebo. 2. reduce the risk of the combined event of "vascular" death, myocardial infarction, or stroke during the first 6 months by a 25% relative risk reduction, relative to placebo

Timeline

Start
2005-06
Primary completion
2010-09
Completion
2010-09

Outcome

Missed primary endpoint

paper composite vascular endpoint did not differ between treatment groups (candesartan, 120 events, vs placebo, 111 events; adjusted hazard ratio 1·09, 95% CI 0·84-1·41; p=0·52). PMID 21316752 ↗

paper functional outcome suggested a higher risk of poor outcome in the candesartan group (adjusted common odds ratio 1·17, 95% CI 1·00-1·38; p=0·048 [not significant at p≤0·025 level]) PMID 21316752 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Candesartan Unknown 16 mg —

Indications