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
Study Type
OBSERVATIONAL
Enrollment
212
Ziekenhuis Netwerk Antwerpen
Antwerp, Belgium
Erasmus MC
Rotterdam, Netherlands
E. Meshalkin National medical research center
Novosibirsk, Russia
Procedure time
Procedure time (minutes)
Time frame: During ablation procedure
Fluoroscopy time
Fluoroscopy time (minutes)
Time frame: During ablation procedure
Transseptal time
Transseptal time (time from insertion of catheters until transseptal puncture) (minutes)
Time frame: During ablation procedure
Left atrial dwell time
Left atrial dwell time (time from LA entry until removal of catheters) (minutes)
Time frame: During ablation procedure
PVI ablation time
PVI ablation time (total PVI ablation time, i.e. first until last application) (minutes)
Time frame: During ablation procedure
Ablation time per pulmonary vein
Ablation time per pulmonary vein (minutes)
Time frame: During ablation procedure
First Pass Isolation
First Pass Isolation (i.e. Successful isolation of PVs after the first ablation attempt)
Time frame: During ablation procedure
Acute success
Acute success (Successful electrical isolation of PVs at the end of procedure)
Time frame: During ablation procedure
TouchUp rates
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
TouchUp rates (additional applications for successful PV isolation)
Time frame: During ablation procedure
Long-term success
Long-term success (freedom of atrial fibrillation 12 months after ablation)
Time frame: From the date of procedure until 1 year
Procedure-related adverse-events
Procedure-related adverse-events
Time frame: From the date of procedure until 7 days
Long-term adverse events
Long-term adverse events
Time frame: From the date of procedure until 1 year