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Taking people in SwitzerlandPhase 3

Tests colchicine to see if atrial fibrillation returns after a heart rhythm shock

Tests colchicine against a placebo in adults with atrial fibrillation after cardioversion.

Plain-language title generated from the registry record
Registry title: Colchicine After Electrocardioversion for Atrial Fibrillation

Key facts

Where
Basel, Bern, Bruderholz, Lausanne, Lucerne, Olten, Rheinfelden, and Solothurn, SwitzerlandSee the 8 sites
Phase
Phase 3

Where in Switzerland

  • University Hospital BaselBasel, SwitzerlandTaking people
  • University Hospital BernBern, SwitzerlandTaking people
  • Cantonal Hospital Baselland (KSBL)Bruderholz, SwitzerlandTaking people
  • Lausanne University HospitalLausanne, SwitzerlandTaking people
  • Lucerne Cantonal HospitalLucerne, SwitzerlandTaking people
  • Cantonal Hospital OltenOlten, SwitzerlandTaking people
  • Herzpraxis am RheinRheinfelden, SwitzerlandTaking people
  • Solothurner Spitäler AGSolothurn, SwitzerlandTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT05890664EU 2024-516033-12-00
Record updated
28 May 2025
Original description
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.Read full original descriptionShow less

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

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.

Inclusion: Age \>18 years; ECG-documented AF prior to ECV; Successful ECV with conversion of AF to sinus rhythm with persistent sinus rhythm ≥30 minutes after ECV; Ability to give written informed consent.

Exclusion: Pulmonary vein isolation within 3 months prior to ECV or pulmonary vein isolation planned within 3 months after ECV; Intake of a strong inhibitor of CYP3A4 or P-Glycoprotein (clarithromycin, erythromycin, telithromycin, cyclosporine, ketoconazole or itraconazole); Known intolerance or hypersensitivity to Colchicine; Serious gastrointestinal disease (severe gastritis or diarrhea); Clinically overt hepatic disease; Significant immunosuppression (e.g. due to transplantation or rheumatic disease); Severe renal disease (eGFR\< 30ml/min/1.73m2); AF persistence after cardioversion or early AF recurrence within 30 minutes after ECV; Any other rhythm than AF before cardioversion; Any other absolute indication for Colchicine intake; Clinically significant blood dyscrasia (e.g., myelodysplasia); Pregnant or breastfeeding women, or women of child-bearing potential who do not use a highly effective form of birth control; Life expectancy \<1 year.

ClinicalTrials.gov NCT05890664 · EU CTIS 2024-516033-12-00