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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
StatusNot Yet Recruiting
PhaseNot applicable
Started
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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.

Record History

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  1. Eligibility criteria shortened, about 12 wordsv2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07036068
Lead Sponsor Shanghai MicroPort EP MedTech Co., Ltd.
Conditions
(from sponsor)		 Paroxysmal Atrial Fibrillation (PAF)
Related terms Atrial Fibrillation
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov