Actively Recruiting

Age: 18Years +
All Genders
ID07109141

Registry of Atrial Arrhythmia Ablation Procedures Using Pulsed Field Ablation in Poland

Led by Wroclaw Medical University · Updated on 2025-08-07

500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are establishing a nationwide registry in Poland to collect data on atrial arrhythmia ablation procedures using Pulsed Field Ablation (PFA). This tissue-selective method targets myocardial cells and has shown promise in treating paroxysmal atrial fibrillation and other arrhythmias such as atrial flutter, atrial tachycardia, and ventricular tachycardia. The registry aims to expand knowledge about the safety and effectiveness of PFA beyond pulmonary vein isolation. The registry includes patients undergoing PFA ablation procedures tailored to their specific arrhythmias. Participation involves standard clinical care without additional procedures during hospitalization. Following the ablation, patients will be monitored for 12 months through telephone interviews at 3, 6, and 12 months. If needed, in-person evaluations may be conducted at the treatment center. Participants will contribute clinical data to better understand procedural techniques and outcomes. Researchers will measure the recurrence of supraventricular arrhythmias over a 12-month period. This registry will support future clinical trials and is coordinated by the Institute for Heart Diseases at the Jan Mikulicz-Radecki University Hospital, with participation from multiple centers performing PFA in Poland.

CONDITIONS

Brief Title

Registry of Atrial Arrhythmia Ablation Procedures Using Pulsed Field Ablation in Poland

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Informed consent obtained from the participant
  • Subject is undergoing ablation of an atrial arrhythmia using the Pulsed Field Ablation (PFA)
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Screening and enrollment visit

Implementation

Duration - Hospitalization period

Participants undergo a Pulsed Field Ablation (PFA) procedure targeting atrial arrhythmias as part of standard clinical care.

1 procedure visit (in-person)

Long-term Monitoring

Duration - 12 months

Participants are followed for 12 months after the ablation procedure to monitor clinical outcomes and arrhythmia recurrence.

Telephone interviews at 3, 6, and 12 months with possible in-person clinical evaluations if needed

Trial Site Locations

Total: 1 location

1

Clinical Department of Cardio, Jan Mikulicz Radecki University Hospital in Wroclaw

Wroclaw, Lower Silesian Voivodeship, Poland, 50-556

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Research Team

S

Stanislaw Tubek, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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