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Clinical Trials/NCT04715425
NCT04715425
Recruiting
Not Applicable

Thoracoscopic Surgical Versus Catheter Ablation Approaches for Primary Treatment of Persistent Atrial Fibrillation

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)3 sites in 1 country170 target enrollmentSeptember 25, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation, Persistent
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Enrollment
170
Locations
3
Primary Endpoint
Freedom of AF, defined as absence of any atrial tachyarrhythmia
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
September 25, 2019
End Date
September 2028
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

J.R. de Groot

prof. dr. J.R. de Groot

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Eligibility Criteria

Inclusion Criteria

  • Age is between 18 and 80 years
  • Persistent AF as defined following the ESC 2016 Guidelines, evidenced by 1) ongoing AF on the ECG or 2) documentation of AF necessitating cardioversion.
  • AF documented by ECG or Holter \< 1 year ago.
  • At least one class I or III anti-arrhythmic drug in standard dosage has failed or is not tolerated.
  • Left atrial volume index ≤ 45 ml/m2
  • Legally competent and willing to sign the informed consent.
  • Willing and able to adhere to the follow-up visit protocol.
  • Life expectancy of at least 2 years.

Exclusion Criteria

  • Prior intervention (catheter ablation or minimally-invasive thoracoscopic ablation) for AF.
  • AF is secondary to electrolyte imbalance, thyroid disease or other reversible or non-cardiovascular causes.
  • Documentation of CTI dependent atrial flutter
  • Valvular AF
  • Paroxysmal AF
  • Long standing Persistent AF, defined as AF continuously present for longer than 1 year.
  • Body mass index \>35kg/m2
  • NYHA class IV heart failure symptoms or left ventricular ejection fraction \<35%.
  • NYHA class III heart failure symptoms, unless caused or aggravated by AF.
  • Myocardial infarction within the preceding 2 months.

Outcomes

Primary Outcomes

Freedom of AF, defined as absence of any atrial tachyarrhythmia

Time Frame: Up until 72 patients experienced AF recurrence

The primary endpoint of the study is freedom of AF, defined as absence of any atrial tachyarrhythmia without the use of antiarrhythmic drugs once a total number of 72 patients with AF recurrences after a single procedure have been reached. This is an event based endpoint. Freedom of atrial tachyarrhythmia is defined as the absence of documentation of episodes of atrial tachyarrhythmia lasting more than 30 seconds on Holter recordings during follow-up and/or on ECGs recorded outside the scope of the study.

Secondary Outcomes

  • One year freedom of AF(1 year of follow-up)
  • Freedom of AF after two procedures(1 year of follow-up after the second procedure)
  • Quality of life after a thoracoscopic surgical procedure or a catheter ablation procedure.(Yearly until 5 years follow-up)
  • Long term freedom of AF(5 years of follow-up)
  • Cost-effectiveness(1 year of follow-up)

Study Sites (3)

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