Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05890664

Colchicine After Electrocardioversion for Atrial Fibrillation

Colchicine After Electrocardioversion for Atrial Fibrillation - The COLECTRO-AF Trial

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
416 (estimated)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate whether a 3 month treatment course of low-dose Colchicine decreases the recurrence of Atrial fibrillation (AF) after electrocardioversion (ECV) in patients with AF.

Detailed description

Atrial fibrillation is the most common cardiac arrhythmia worldwide and is associated with an increased risk of heart failure, stroke and death. Over the next 40 years the investigators expect another increase in the prevalence of atrial fibrillation with a risk of 1:3 in people over 65 years to develop atrial fibrillation. Electroconversion can occur in patients with atrial fibrillation reestablish sinus rhythm acutely with a controlled electrical shock. Unfortunately it is known however, that there is a short-term recurrence of atrial fibrillation in about 60%. This underlines that our current treatment options are inadequate. There is increasing evidence that inflammation is integral to initiation and maintenance of atrial fibrillation. Therefore, the researchers see inflammation as a possible therapeutic target to reduce the recurrence rate of atrial fibrillation after electroconversion. To test this hypothesis and to help patients, the investigators want to conduct the COLECTRO-AF study.

Conditions

Interventions

TypeNameDescription
DRUGColchicineColchicine 0.5 mg (oral) once daily for 90 days. The chemical name for colchicine is (S)-N-(5,6,7,9-tetrahydro-1,2,3,10-tetramethoxy-9 oxobenzol\[a\]heptalen-7-yl) acetamide. Colchicine consists of pale yellow scales or powder. It is soluble in water, freely soluble in alcohol, and slightly soluble in ether.
DRUGPlaceboMatched placebo. Both the active drug and placebo will look similarly. The route and mode of administration is also similar to the active group.

Timeline

Start date
2024-04-14
Primary completion
2027-03-01
Completion
2027-03-01
First posted
2023-06-06
Last updated
2025-05-28

Locations

8 sites across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT05890664. Inclusion in this directory is not an endorsement.