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Study identifier: NCT06656884 Synced from ClinicalTrials.gov · August 03, 2026
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FARAPULSE Workflow Assessment Registry

Condition: Atrial Fibrillation (AF)  ·  Sponsor: Boston Scientific Corporation

PhaseN/A
Planned participants524
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The study is designed to determine the best practices in the patient pathway, and to analyze pre-procedural, procedural and follow-up workflow data related with ablation of atrial fibrillation where the FARAPULSE™ Pulsed Field Ablation System is used in a commercial and standard of care setting. Workflow-related variables, inclusive of pre-procedural imaging, methods of transseptal access, anesthesia/sedation technique, intracardiac mapping, ablation settings, dosing strategy, lesion sets and general procedure management, will be used to identify predominant workflow schemes that will be associated with patient demographics, procedure-related complications (safety parameters), and one-year effectiveness parameters. The study data can be used for procedural workflow optimization when using Pulsed Field Ablation for the ablation treatment of Atrial Fibrillation based on patient demographics, cardiac anatomy and arrhythmia characteristics.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

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Locations (28)

A.o. Krankenhaus der Elisabethinen LinzLinz, Austria
Ziekenhuis aan de Stroom, MiddelheimAntwerp, Belgium
Ziekenhuis Oost-LimburgGenk, Belgium
CHR de la CitadelleNamur, Belgium
CHU de BordeauxBordeaux, France
Hopital Saint PhilibertLomme, France
CHRU Hopital TrousseauTours, France
Universitaetsklinikum DusseldorfDüsseldorf, Germany
Staedtisches Klinikum KarlsruheKarlsruhe, Germany
Munchen Klinik BogenhausenMünchen, Germany
Ippokrateio General Hospital of AthensAthens, Greece
Mitera HospitalAthens, Greece

+ 16 more locations — full list on the registry record.

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