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NCT06333327Recruiting

Multicenter Registry of Atrial Fibrillation Ablation With Radiofrequency Balloon Catheter

Multielectrode Radiofrequency Balloon for Atrial Fibrillation Catheter Ablation: A Multicenter Real-World Experience
Universitair Ziekenhuis BrusselClinicalTrials.govdeviceDevice trial
Study focus
Disease/Condition
Atrial Fibrillation
Drug/Device/Intervention
Pulmonary vein isolation with the multielectrode radiofrequency balloon catheter
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
Universitair Ziekenhuis Brussel
Location
Brussels, Belgium
Timeline & enrollment
Phase
N/A
Start date
Jan 01, 2021
End date
Dec 01, 2030
Enrollment
2000 participants
Primary outcome

Atrial arrhythmia recurrence after ablation,Procedural safety

Summary

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.

ICD-10 classifications
Chronic atrial fibrillationPersistent atrial fibrillationParoxysmal atrial fibrillationAtrial fibrillation and flutterAtrial fibrillation and atrial flutter, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06333327
Type
Device Trial
About this record

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.