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Observes a balloon catheter procedure to treat irregular heartbeat in atrial fibrillation

Follows adults with atrial fibrillation who receive a radiofrequency balloon catheter treatment.

Plain-language title generated from the registry record
Registry title: Multicenter Registry of Atrial Fibrillation Ablation With Radiofrequency Balloon Catheter

Key facts

Where
Brussels, BelgiumSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with symptomatic atrial fibrillation who are having catheter ablation with the Heliostar radiofrequency balloon catheter.

Age
18 to 85 years
Sex
All sexes can join
Disease stage
Paroxysmal or persistent atrial fibrillation with symptoms and an indication for catheter ablation

Main reasons for not taking part

  • Under 18 years old
  • Pregnancy
  • Any contraindication to catheter ablation

Read by machine on 9 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 85 years old?

Source: NCT06333327, who can take part

Where in Belgium

  • UZ Brussel Heart Rhythm Management CenterBrussels, BelgiumContact: Carlo de Asmundis, MD, PhDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Universitair Ziekenhuis Brussel
Trial code
NCT06333327
Record updated
27 March 2024
Original description
All consecutive patients with paroxysmal or persistent atrial fibrillation undergoing pulmonary vein isolation with the radiofrequency balloon catheter (RFB) "Heliostar" (Biosense Webster) will be included in a multicenter observational registry. The aim of the study is to assess the safety and arrhythmic outcome of atrial fibrillation ablation with the RFB in a real-world setting.Read full original descriptionShow less

Multielectrode Radiofrequency Balloon for Atrial Fibrillation Catheter Ablation: A Multicenter Real-World Experience

All consecutive patients with paroxysmal or persistent atrial fibrillation undergoing pulmonary vein isolation with the radiofrequency balloon catheter (RFB) "Heliostar" (Biosense Webster) will be included in a multicenter observational registry. The aim of the study is to assess the safety and arrhythmic outcome of atrial fibrillation ablation with the RFB in a real-world setting.

Inclusion: symptomatic atrial fibrillation with indication to catheter ablation.

Exclusion: age <18 years old; pregnancy; any contraindications to catheter ablation.

ClinicalTrials.gov NCT06333327