Convergent Ablation Plus Left Atrial Appendage Isolation for the Treatment of Persistent Atrial Fibrillation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorBarts & The London NHS Trust

About this trial

A randomised controlled clinical trial to assess efficacy of convergent ablation with the LARIAT procedure, as compared to standard endocardial catheter ablation in patients with long-standing persistent atrial fibrillation (AF).

Eligibility criteria

Qualifiers

Age > 18 years; < 80 years

Persistent AF > 1-year duration

Left atrium size < 6cm

Pts should be able to provide written informed consent.

Disqualifiers

Subjects currently enrolled in another investigational study except in case of observational registry with no associated treatments.

Subject has a reversible cause of AF or transient AF

Subject is absent of LAA or if the LAA is previously surgically ligated

Subject has had previous cardiac surgery or abdominal surgery.

Trial design

Treatments tested in this trial

  • Epicardial AF ablation using AtriCure EPi-Sense-AF Guided Coagulation System with Left Atrial Appendage Exclusion using the AtriCure LARIAT Suture Delivery Device.
  • Standard Endocardial Catheter Ablation

Treatment groups

48 Participants
are divided into 2 treatment groups

Sponsors and collaborators