drugset / Trial / NCT00130975

Candesartan in the Prevention of Relapsing Atrial Fibrillation

NCT00130975 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to test the hypothesis that treatment with the angiotensin II type 1 receptor antagonist candesartan may reduce the recurrence rate of atrial fibrillation after electrical cardioversion.

Timeline

Start
2001-04
Primary completion
—
Completion
2005-09

Outcome

Missed primary endpoint

paper Treatment with the ARB candesartan for 3-6 weeks before and 6 months after electrical cardioversion had no effect on the recurrence rate of AF. PMID 17113170 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Candesartan Unknown 16 mg —

Indications