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Hybrid AbLaTion of Atrial Fibrillation — HALT-AF  

Atrial Fibrillation Clinical Trial

Official title:
A Randomised Controlled Trial Comparing Hybrid Convergent Ablation to Standard Catheter Ablation in Patients With Non-Paroxysmal Atrial Fibrillation

Clinical Trial Summary

A randomised controlled trial to assess the efficacy of staged hybrid ablation when compared with standard catheter ablation in patients with non-paroxysmal atrial fibrillation (AF)

Clinical Trial Description

The objective of this randomized study is to evaluate the safety and efficacy of Convergent hybrid ablation when compared to standard catheter ablation in patients with non-paroxysmal AF. Patients will be randomised in a 1:1 ratio. The primary efficacy endpoint will be freedom from persistent atrial arrhythmia (measured from the end of a 3-month blanking period up to 24 months (12 and 24 months). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05411614
Study type Interventional
Source St. George's Hospital, London
Contact Riyaz A Kaba
Phone 020 8725 4571
Email rkaba@sgul.ac.uk
Status Recruiting
Phase N/A
Start date May 1, 2022
Completion date October 2027
View Details
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