Clinical Trial

Deliver mOre aPplications for More Durable Pulmonary Vein IsOlation

Study acronym: DOPPIO
Active, Not Recruiting
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Summary
Pulmonary vein isolation (PVI) by catheter ablation (CA) has become a widely accepted interventional treatment for patients with symptomatic atrial fibrillation (AF) despite anti-arrhythmic drugs (AAD). Classic thermal ablation modalities use radiofrequency energy or cryo-energy to create cardiac tissue lesions. Irreversible electroporation (IRE) using pulsed field energy (PFA) is a novel technology for cardiac tissue ablation. Initial studies have shown favorable outcome data in patients with AF treated by performing PVI using PFA. However, the freedom of AF has not yet proven superior to existing thermal ablation methods and appears similarly associated with suboptimal lesion durability, leading to electrical reconnection. The purpose of this study is to determine if freedom of atrial fibrillation may be improved by delivering more and better targeted pulsed field ablations.
Protocol Amendment History 1 change
critical Enrollment closed, study ongoing 2026-08-12
Trial Details
NCT Number NCT07021313
Lead Sponsor R&D Cardiologie
Conditions Atrial Fibrillation
Enrollment 378 participants
Start Date 2025-06-30
Primary Completion 2027-06-30 (estimated)
Study Completion 2028-06 (estimated)
Updated on ClinicalTrials.gov 2026-08-11