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Clinical Efficacy of Ablation of Slow Conduction and Low-Voltage Myocardium Under Rapid Atrial Pacing Combined with Pulmonary Vein Isolation Guided by Omnipolar Technology in Patients with Long-Standing Persistent Atrial Fibrillation

Clinical Efficacy of Ablation of Slow Conduction and Low-Voltage Myocardium Under Rapid Atrial Pacing Combined with Pulmonary Vein Isolation Guided by Omnipolar Technology in Patients with Long-Standing Persistent Atrial Fibrillation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119636
Enrollment
Unknown
Registered
2026-03-02
Start date
2026-03-06
Completion date
Unknown
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Interventions

PVI + Novel Substrate Modification Group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age >=18 years and =2 years). 3.Willingness to provide written informed consent. 4. Willingness to undergo the procedure and postoperative follow-up.

Exclusion criteria

Exclusion criteria: 1.Prior history of catheter ablation for atrial fibrillation. 2. Planned or prior left atrial appendage closure during the same period. 3. History of cardiac surgery or thoracotomy within the past 3 months. 4. Thrombocytopenia (platelet count 50 mm (measured by two-dimensional echocardiography in the parasternal long-axis view). 7. Presence of left atrial thrombus (confirmed by transesophageal echocardiography or multi-detector computed tomography). 8. Concomitant severe structural heart disease, including: severe mitral regurgitation; clinically significant valvular heart disease; congenital heart disease. 9. Autoimmune diseases (e.g., systemic lupus erythematosus, scleroderma). 10. Active malignancy. 11. Systemic active infection (deemed unsuitable for interventional therapy by the investigator). 12. Pregnancy. 13. Life expectancy <12 months.

Design outcomes

Primary

MeasureTime frame
Surgical success rate at 12 months post-operation;

Secondary

MeasureTime frame
Immediate procedural ablation success rate;

Countries

China

Contacts

Public ContactKaijun Cui

West China Hospital, Sichuan University

cuikaijunscu@163.com+86 189 8060 2036

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026