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ADVENT Post-Approval Study — ADVENT PAS  

Paroxysmal Atrial Fibrillation Clinical Trial

Official title:
Prospective, Multi-site Safety and Effectiveness Post-Approval Study of FARAPULSE Pulsed Field Ablation in Paroxysmal Atrial Fibrillation

Clinical Trial Summary

The ADVENT Post Approval Study (PAS) is a prospective, global, multicenter, observational study.

Clinical Trial Description

The objective of ADVENT PAS is to evaluate the long-term safety and effectiveness profile of the FARAPULSE Pulsed Field Ablation System when used to perform pulmonary vein isolation (PVI) in the de-novo ablation treatment of patients with paroxysmal atrial fibrillation (PAF). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06431815
Study type Observational
Source Boston Scientific Corporation
Contact Erin L Feddema, MPH
Phone +1 651-582-5077
Email erin.feddema@bsci.com
Status Not yet recruiting
Phase
Start date October 2024
Completion date October 2029
View Details
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