← Eichor
Study identifier: NCT07021313 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Deliver mOre aPplications for More Durable Pulmonary Vein IsOlation

Condition: Atrial Fibrillation  ·  Sponsor: R&D Cardiologie

PhaseNA
Planned participants378
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Lucas VA Boersma, MD, PhD  ·  +31883200900  ·  L.boersma@antoniusziekenhuis.nl

Isabelle N Bax, MD  ·  +31883200929  ·  i.bax@antoniusziekenhuis.nl

Always discuss trial participation with your own doctor first.

Locations (1)

St. Antonius HospitalNieuwegein, NetherlandsRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07021313