Actively Recruiting
Thoracoscopic Surgical Versus Catheter Ablation Approaches for Primary Treatment of Persistent Atrial Fibrillation
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-01-25
170
Participants Needed
3
Research Sites
466 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Rationale: Atrial fibrillation (AF) is a highly prevalent cardiac arrhythmia. AF is classified as paroxysmal or persistent AF, based on the duration and persistency of the arrhythmia. Despite state-of-the-art pharmacological therapies targeting the ventricular rate or aiming to restore sinus rhythm, many patients with persistent AF stay symptomatic. Catheter ablation, endocardial pulmonary vein isolation (PVI) in particular, is the most commonly applied approach to treat drug refractory persistent AF, but particularly in this patient group results are modest. Alternatively, the PVs can be approached epicardially by thoracoscopic surgery to isolate the PVs. This approach is more efficacious, at the cost of a more invasive procedure and longer hospital stay. However, no studies have been conducted comparing catheter with thoracoscopic ablation in patients with persistent AF as a primary invasive procedure after failing treatment with anti-arrhythmic medication. Objective: This current study aims to assess a patient specific therapy plan for patients with persistent AF by randomizing thoracoscopic versus catheter ablation for PVI without adjuvant substrate ablation in those patients. Study design: This is a prospective, non-blinded randomized multicenter study. Subjects will be randomized (1:1) to one of the two study-arms (thoracoscopic surgical or catheter PVI). The follow-up will last 5 years, with heart rhythm monitoring at three and six months, one year and yearly in the following years. In case AF recurs during the first year, the subject will receive the treatment of the otherother arm, or according to patient choice or clinical routine. Study population: Patients with an indication for invasive treatment of persistent AF. Intervention: Thoracoscopic surgical or catheter PVI without additional lesions.
CONDITIONS
Official Title
Thoracoscopic Surgical Versus Catheter Ablation Approaches for Primary Treatment of Persistent Atrial Fibrillation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age is between 18 and 80 years
- Persistent atrial fibrillation confirmed by ECG or documentation requiring cardioversion
- AF documented by ECG or Holter less than 1 year ago
- At least one class I or III anti-arrhythmic drug has failed or is not tolerated
- Left atrial volume index 45 ml/m2 or less
- Legally competent and willing to sign informed consent
- Willing and able to follow study visit schedule
- Life expectancy of at least 2 years
You will not qualify if you...
- Prior catheter or thoracoscopic ablation for atrial fibrillation
- AF caused by electrolyte imbalance, thyroid disease, or reversible/non-cardiovascular causes
- CTI dependent atrial flutter documented
- Valvular atrial fibrillation
- Paroxysmal atrial fibrillation
- Long-standing persistent AF present continuously for over 1 year
- Body mass index over 35 kg/m2
- NYHA class IV heart failure symptoms or left ventricular ejection fraction below 35%
- NYHA class III heart failure symptoms unless caused or worsened by AF
- Myocardial infarction within last 2 months
- Active infection or sepsis
- Known carotid stenosis over 80%
- Planned cardiac surgery other than for AF
- Pregnancy or childbearing potential without contraception
- Need for anti-arrhythmic drugs for ventricular arrhythmias
- Intracardiac mass or thrombus discovered after consent
- Conditions increasing risk of general anesthesia or port access surgery
- Previous thoracic radiation therapy
- Inability to follow-up
- No vascular access for catheterization
- Previous thoracotomy
- Factors preventing transseptal puncture for catheterization
AI-Screening
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Trial Site Locations
Total: 3 locations
1
Amsterdam University Medical Center location AMC
Amsterdam, Netherlands
Actively Recruiting
2
Maastricht UMC+
Maastricht, Netherlands
Not Yet Recruiting
3
St. Antonius Ziekenhuis Nieuwegein
Nieuwegein, Netherlands
Actively Recruiting
Research Team
J
J.R. de Groot, MD PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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