PFA for Paroxysmal Atrial Fibrillation

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to verify the safety and efficacy of the cardiac pulse ablation system in paroxysmal atrial fibrillation to provide the basis for product registration and clinical application. The trial will be conducted at a clinical center with appropriate clinical cases, and paroxysmal atrial fibrillation ablation procedures will be performed by an authorized investigator using the trial product. The effectiveness and safety of the cardiac pulse ablation system in the treatment of paroxysmal atrial fibrillation will be verified by collecting the treatment success rate, immediate ablation success rate, procedure time and device use evaluation within 12 months after the procedure.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05618340
Study type	Interventional
Source	Shanghai Shangyang Medical Technology Co., Ltd.
Contact
Status	Active, not recruiting
Phase	N/A
Start date	September 26, 2022
Completion date	September 1, 2025

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