Ablation of Fibrotic Areas in Patients With Persistent Atrial Fibrillation.

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    Karolinska University Hospital
Updated on 19 February 2024
dyspnea
atrial fibrillation
radiofrequency ablation
persistent atrial fibrillation
catheter ablation
fibrillation
antiarrhythmic drug
pulmonary vein isolation

Summary

Brief summary: The objective of this study is to compare two different ablation strategies in participants with persistent atrial fibrillation and fibrotic areas in the left atrium. The participant will be randomized to pulmonary vein isolation or pulmonary vein isolation plus ablation of fibrotic areas.

Description

Background

Atrial fibrillation (AF) is the most common arrhythmia in clinical practice with a prevalence of 2-3 percent in the population. Catheter ablation performing pulmonary vein isolation (PVI) is an established treatment, which aim to eliminate triggers from the pulmonary veins. This treatment is successful in most patients with paroxysmal AF. In many patients, especially the patients with persistent AF, this treatment is not sufficiently to achieve freedom from arrhythmia and symptoms.

There are several studies showing that fibrosis in the left atrium (LA) is an independent factor to relapse in AF after PVI. The fibrotic areas can be detected by measuring the voltage in the left atrium and creating a voltage map. There are non-randomized studies that suggest better results regarding reduction of arrhythmia burden after ablating the low voltage areas (LVAs). This ablation strategy is commonly used in clinical praxis although there are no randomized studies in this field.

Aim

The objective of this study is to compare two different ablation strategies in participants with persistent atrial fibrillation and fibrotic areas in the left atrium. The participant will be randomized to PVI versus PVI plus ablation of LVAs.

The primary endpoint is freedom of atrial arrhythmias after 1 to 2 ablation procedures within 6 months measured at 12 months after the first ablation procedure without antiarrhythmic drugs. Secondary endpoints will be atrial arrhythmia burden, health related quality of life measured by AFEQT score, and RAND 36 and periprocedural complications; death, stroke/ TIA, tamponade, atrio-esophageal fistula, and atrioventricular block.

Study design:

Randomized controlled multicenter trial. The study will be single blinded. All the participants will undergo PVI and the substrate map will be collected during atrial pacing. The patients with LVA will be randomized in a 1:1 fashion to; PVI plus ablation of LVA or PVI alone. Follow up visits will be at 3, 6, 12, 18 and 24 months. Before ablation and at every follow up visit the participants will fill in arrhythmia symptom specific questionnaires (AFEQT and ASTA) and questionnaire about quality of life (RAND 36). The participants will register arrhythmia with a heart monitoring system if symptoms of arrhythmia and two times daily during two weeks before every follow up visit.

Details
Condition Arrhythmia, Arrhythmia, Atrial Fibrillation, Atrial Fibrillation, atrial fibrillation (pediatric), atrial fibrillation (pediatric)
Age 18years - 100years
Treatment Radio frequency ablation
Clinical Study IdentifierNCT04377594
SponsorKarolinska University Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

ECG-documented persistent or long-standing persistent atrial fibrillation according to European Society of Cardiology (ESC) definition
Symptoms e. g. palpitations, dyspnea, tiredness that is due to the atrial fibrillation
Suitable candidate for catheter ablation
Tried one or more antiarrhythmic drugs or unwilling to try antiarrhythmic drugs
Age 18 years

Exclusion Criteria

LA dimension >55 mm as determined by an echocardiography within the previous year
Acute coronary syndrome or coronary artery bypass surgery within 12 weeks
Severe aortic or mitral valvular heart disease using the ESC guidelines
Congenital heart disease
Prior surgical or percutaneous AF ablation procedure or atrioventricular-nodal ablation
Medical condition likely to limit survival to < 1 year
New York Heart Association (NYHA) class IV heart failure symptoms
Contraindication to oral anticoagulation
Renal failure requiring dialysis
AF due to reversible cause
Pregnant and fertile women without anticonception
History of non-compliance to medical therapy
Unable or unwilling to provide informed consent
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