Candesartan in the Prevention of Relapsing Atrial Fibrillation

Phase 3

Completed

• Conditions: Atrial Fibrillation

• Registration Number: NCT00130975
• Lead Sponsor: Asker & Baerum Hospital

Brief 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.

Detailed Description

Background: The most effective procedure to restore sinus rhythm in patients with persistent atrial fibrillation (AF) is electrical cardioversion, but AF recurs in 60-80% of the patients during the first year. AF is associated with electrical and anatomical remodelling of the atria, and angiotensin II is involved in the remodelling process. Studies have indicated that the angiotensin II type 1 receptor antagonist candesartan may counteract both electrical and anatomical remodelling induced by AF. The investigators therefore hypothesised that treatment with candesartan may reduce the recurrence rate of AF after electrical cardioversion.

Study design: 171 patients with persistent AF scheduled for electrical cardioversion are randomised in a double blind, placebo-controlled study. The patients receive tablets of candesartan 8 mg or matching placebo once daily for 3-6 weeks before cardioversion, and candesartan 16 mg or matching placebo once daily for 6 months after cardioversion. The study medication is discontinued if electrical cardioversion is unsuccessful or if AF recurrence is documented. Primary endpoint is recurrence of AF. Clinical, electrocardiographic, echocardiographic and biochemical markers will be analysed.

Study Timeline

• Study Start: 2001-04
• Study First Submitted: 2005-08-16
• Study First Submitted QC: 2005-08-16
• Study First Posted: 2005-08-17
• Study Completion: 2005-09
• Status Verified: 2007-01
• Last Update Submitted: 2007-01-03
• Last Update Posted: 2007-01-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

• Patients with atrial fibrillation, diagnosed electrocardiographically, of more than 48 hours duration in whom direct current (DC) cardioversion is planned.

Exclusion Criteria

• Patients with a history of known hypersensitivity or contraindication to any angiotensin II receptor blocker or any angiotensin-converting enzyme (ACE) inhibitor.
• Patients currently receiving an ACE inhibitor or angiotensin II antagonist because of heart failure or other strong indication.
• Patients currently receiving any antiarrhythmic medication including sotalol. Other beta-blockers will not be regarded as specific antiarrhythmic agents.
• Significant renal artery stenosis and any medical condition in which administration of a vasodilator is contraindicated; serum creatinine > 225 micromol/L; or serum potassium > 5.5 mmol/L; or serum sodium < 128 mmol/L.
• Patients with severe hepatic dysfunction.
• Life-limiting disease or substance abuse which may affect participation.
• Patients unwilling to participate.
• Patients who have previously undergone DC cardioversion for atrial fibrillation within the last month.
• Thyrotoxicosis.
• Patients with a systolic blood pressure of < 100 mm Hg.
• Hypertensive patients requiring intensified treatment prior to DC cardioversion.
• Pregnancy or lactation.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Recurrence of atrial fibrillation

Secondary Outcome Measures

Name	Time	Method
Time to recurrence of atrial fibrillation

Trial Locations

Locations (2)

Ulleval University Hospital; 🇳🇴 Oslo, Norway

Asker & Baerum Hospital; 🇳🇴 Rud, Norway