COAST-AF
Characterization of Arrhythmia Substrate to Ablate Persistent Atrial Fibrillation
Objective
A multicentre, parallel group, two arm, single-blinded randomized clinical trial, assessing the efficacy of a patient-tailored catheter ablation (CA) strategy guided by atrial scar mapping in addition to pulmonary vein isolation (PVI) when compared to PVI alone in patients with persistent atrial fibrillation (AF).
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Inclusion
- Age ≥18 years ;
- Subjects with symptomatic persistent AF AND clinically indicated catheter ablation for AF
- At least one episode of AF that is sustained beyond 3 months in duration ; documented on 12-lead ECG, Holter monitor, loop monitor or trans-telephonic monitor (TTM) within 36 months of enrollment in the study;
- Modified DR-FLASH score ≥3
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Exclusion
- History of previous catheter ablation for AF or left atrial flutter;
- History of previous surgical ablation for AF;
- Known intracardiac thrombus;
- Contraindication to systemic oral anticoagulation therapy;
- Reversible causes of AF;
- Hypertrophic cardiomyopathy;
- Severe valvular disease (mitral/aortic stenosis or regurgitation);
- Subjects that are pregnant or breastfeeding;
- Comorbid condition with life expectancy < 1 year
Additional Info
Ethics ID: REB18-1762
ClinicalTrials.gov ID: NCT03347227
Sponsor: Ottawa Heart Institute Research Corporation
PI: Dr. George Veenhuyzen
Phone: 403 944 3385
Admin: Jennifer McKeage
Phone: 403 210 6047
Email: jmckeage@ucalgary.ca
Updated May 2, 2024