The purpose of this observational registry is to prospectively collect procedure efficiency, safety and acute and long term outcome data from catheter ablation procedures as treatment of paroxysmal atrial fibrillation, using the following treatment modalities: * Cryoballoon ablation * Manual guided RF ablation using Contact Force catheters * Remote Magnetic Navigation guided RF ablation with e-Contact and high power settings * Remote Magnetic Navigation guided RF ablation with e-Contact and low power settings
Age range
18 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Procedure time
Timeframe: During ablation procedure
Fluoroscopy time
Timeframe: During ablation procedure
Transseptal time
Timeframe: During ablation procedure
Left atrial dwell time
Timeframe: During ablation procedure
PVI ablation time
Timeframe: During ablation procedure
Ablation time per pulmonary vein
Timeframe: During ablation procedure