Recruiting NA Persistent Atrial Fibrillation

Compares treatment options for Persistent Atrial Fibrillation

Official title PVI Alone Versus PVI Plus PWI and SVCI With PFA

ClinicalTrials.gov ID: NCT07405359

What this study is testing

What it's testing
Catheter based ablation of atrial fibrillation (AF) is an established treatment modality for rhythm control of AF, with pulmonary vein isolation (PVI) being the cornerstone of this technique. While pulmonary vein triggers are the predominant arrhythmia mechanism in paroxysmal AF, development of additional atrial substrate contributes to maintenance of AF in persistent AF.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Age ≥18 years at their pre-procedure visit
  • Persistent AF, defined as at least one continuous AF episode lasting at least seven days in duration, documented by a continuous monitor or 2 ECGs\>7...
  • Indicated and interested in ICM implant for monitoring post ablation
  • Written informed consent obtained from subject and ability for subject to comply with the requirements of the study

You likely can't join if

  • Any prior atrial endocardial or epicardial ablation procedure, other than cavotricuspid isthmus ablation or supraventricular tachycardia
  • Stroke or transient ischemic attack within the previous six months
  • Gastrointestinal bleeding within the previous three months
  • Implanted pacemaker or defibrillator
  • Longstanding persistent AF (\> 3 years)
  • LA volume \>80ml/m2
See the full eligibility criteria
Who can join
  • Age ≥18 years at their pre-procedure visit
  • Persistent AF, defined as at least one continuous AF episode lasting at least seven days in duration, documented by a continuous monitor or 2 ECGs\>7 days apart or ≥3 cardioversions
  • Indicated and interested in ICM implant for monitoring post ablation
  • Written informed consent obtained from subject and ability for subject to comply with the requirements of the study
What rules you out
  • Any prior atrial endocardial or epicardial ablation procedure, other than cavotricuspid isthmus ablation or supraventricular tachycardia
  • Stroke or transient ischemic attack within the previous six months
  • Gastrointestinal bleeding within the previous three months
  • Implanted pacemaker or defibrillator
  • Longstanding persistent AF (\> 3 years)
  • LA volume \>80ml/m2
  • Atrial septal occlusion device
  • Current left atrial thrombus
  • Left atrial appendage occlusion or closure device \< 6 mos or with leak or prior DRT
  • Mitral or Tricuspid valve clip or mechanical replacement or clip
  • Hypertrophic cardiomyopathy
  • Contraindication to femoral vascular access
  • Congenital heart disease with residual anatomic abnormality
  • Contraindication to, or unwillingness to use, systemic anticoagulation
  • Pregnancy
  • Left ventricular ejection fraction \<30%
  • Baseline creatinine \>2.0 mg/dL
  • Predicted life expectancy less than one year
  • Refusal to receive ICM implant or allergy to ICM

The study team makes the final eligibility decision.

Where it's taking place

  • San Francisco, California, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include San Francisco, California, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.