Clinical Trials Directory

Trials / Completed

CompletedNCT02459574

Ablation Verses Anti-arrhythmic Therapy for Reducing All Hospital Episodes From Recurrent Atrial Fibrillation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
321 (actual)
Sponsor
Imperial College London · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

A streamlined AF ablation procedure done without PV mapping as a daycase is more effective than anti-arrhythmic drugs at reducing all hospital episodes for recurrent atrial fibrillation.

Detailed description

AVATAR-AF is a multicentre, randomised controlled study comparing a streamlined AVATAR-protocol ablation procedure to anti-arrhythmic therapy in patients with documented paroxysmal AF who are considered to be failing current strategy for AF. A secondary control arm will also compare the AVATAR-protocol to conventional AF ablation. 300 patients who are on no prior anti-arrhythmic, 'pill-in-pocket' or taking regular anti-arrhythmics will be randomised in a 1:1:1 manner to a treatment strategy of either AVATAR-protocol ablation, anti-arrhythmic therapy or conventional AF ablation and followed-up for 1 year.

Conditions

Interventions

TypeNameDescription
PROCEDUREAVATAR-AF ablationExperimental ablation protocol
DRUGAnti-Arrhythmic therapyGroup 2 will be prescribed medication listed below: Amiodarone; Dronaderone; Sotalol Beta blockers; Calcium channel blockers; Flecainide; or Propafenone. You will then be discharged from clinic. A research nurse will contact you by phone to make sure there are no problems and can make hospital appointments if needed.
PROCEDUREConventional AF ablationConventional ablation procedure

Timeline

Start date
2015-05-01
Primary completion
2018-09-30
Completion
2018-11-27
First posted
2015-06-02
Last updated
2024-10-09
Results posted
2024-10-09

Locations

13 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02459574. Inclusion in this directory is not an endorsement.