ClinicalTrials.Veeva

Menu

Safety and Efficacy of Persistent Atrial Fibrillation Ablation With a Cryoballoon Technology

U

Universitair Ziekenhuis Brussel

Status

Completed

Conditions

Atrial Fibrillation

Treatments

Device: catheter ablation

Study type

Observational

Funder types

Other

Identifiers

NCT06567652
PolarXpersistent

Details and patient eligibility

About

The goal of this retrospective observational study is to learn about the safety and efficacy of cryoballoon catheter ablation in 80 patients with persistent atrial fibrillation using the PolarX (Boston scientific) cryoablation technology. The main question it aims to answer is if it is safe and effective.

Enrollment

80 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • persistent atrial fibrillation patients undergoing first atrial fibrillation ablation procedure with PolarX cryoballoon

Exclusion criteria

  • previous atrial fibrillation ablation or cardiac surgery,
  • paroxysmal atrial fibrillation,
  • congenital heart disease,
  • non-treated coronary artery disease,
  • intracavitary thrombus,
  • significant valvular disease,
  • contraindications to general anesthesia.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems