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Study identifier: NCT06808217 Synced from ClinicalTrials.gov · August 02, 2026
● Active Not Recruiting

A Registry on the FARAVIEW Technology of the OPAL HDx Mapping System When Used With the FARAWAVE NAV Ablation Catheter in the Treatment of Atrial Fibrillation

Condition: Atrial Fibrillation · Pulsed Field Ablation · FARAPULSE  ·  Sponsor: Boston Scientific Corporation

PhaseN/A
Planned participants550
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The study is designed to collect data on the acute and long-term (1 year) safety and effectiveness outcome when an ablation procedure is performed in a commercial and standard of care setting with the FARAPULSE™ Pulsed Field Ablation System, whereby the FARAWAVE NAV Ablation catheter is used in conjunction with the OPAL HDx Mapping System. In addition, the study intends to analyse the association between several workflow-related variables, inclusive of intracardiac electro-anatomical mapping and ablation strategy with procedure-related complications (safety parameters), and one-year effectiveness parameters.

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 (22)

Allgemeines Krankenhaus AKHVienna, Austria
CHRU de Clermont-FerrandClermont-Ferrand, France
CHU GrenobleGrenoble, France
Hospital de la Pitie-SalpetriereParis, France
Hospital Europeen Georges-Pompidou (HEGP)Paris, France
Centre Cardiologique du NordSaint-Denis, France
CHU de Saint-EtienneSaint-Priest-en-Jarez, France
Clinique PasteurToulouse, France
Vivantes Klinikum Am UrbanBerlin, Germany
MVZ CCB Frankfurt und Main-Taunus GbRFrankfurt, Germany
Asklepios Klinik Saint GeorgHamburg, Germany
Henry Dunant Hospital CenterAthens, Greece

+ 10 more locations — full list on the registry record.

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