Clinical Trial

A Clinical Study on the Use of a Domestically Produced Cryoablation System Combined With Balloon Cryoablation Technology for the Treatment of Paroxysmal Atrial Fibrillation

Study acronym: Balloon cryoab
Not Yet Recruiting
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Record status
This record was last updated June 27, 2025 (before its estimated August 31, 2025 completion). Its status may not reflect the trial's current state.
Summary
To validate the safety and efficacy of balloon cryoablation technology and the accompanying disposable intracardiac mapping electrode catheter and adjustable guide sheath for the treatment of paroxysmal atrial fibrillation.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-06-24.
Trial Details
NCT Number NCT07036068
Lead Sponsor Shanghai MicroPort EP MedTech Co., Ltd.
Conditions Paroxysmal Atrial Fibrillation (PAF)
Enrollment 20 participants
Start Date 2025-08-31
Primary Completion 2025-08-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-06-27