Trials / Not Yet Recruiting
Not Yet RecruitingNCT07036068
A Clinical Study on the Use of a Domestically Produced Cryoablation System Combined With Balloon Cryoablation Technology for the Treatment of Paroxysmal Atrial Fibrillation
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Shanghai MicroPort EP MedTech Co., Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | IceMagic™ CryoAblation Catheter | IceMagic™ CryoAblation Catheter is available in two diameters: 23 mm and 28 mm. Each diameter has two types of balloon outer surfaces: with or without multi-channel tissue temperature measurement function. The catheter length is 140 cm, and the tube diameter is 10.5 F. Doctors can choose according to the size of the target pulmonary vein. |
Timeline
- Start date
- 2025-08-31
- Primary completion
- 2025-08-31
- Completion
- 2027-12-31
- First posted
- 2025-06-25
- Last updated
- 2025-06-27
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07036068. Inclusion in this directory is not an endorsement.