Multicenter Registry of Atrial Fibrillation Ablation With Radiofrequency Balloon Catheter
- Disease/Condition
- Atrial Fibrillation
- Drug/Device/Intervention
- Pulmonary vein isolation with the multielectrode radiofrequency balloon catheter
- Study type
- Observational
- Intervention type
- device
- Primary sponsor
- Universitair Ziekenhuis Brussel
- Location
- Brussels, Belgium
- Phase
- N/A
- Start date
- Jan 01, 2021
- End date
- Dec 01, 2030
- Enrollment
- 2000 participants
Atrial arrhythmia recurrence after ablation,Procedural safety
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06333327
- Type
- Device Trial
Access comprehensive clinical trial information for NCT06333327 through Pure Global AI's free database. This phase not specified trial is sponsored by Universitair Ziekenhuis Brussel and is currently Recruiting. The study focuses on Atrial Fibrillation. Target enrollment is 2000 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.