Skip to content

Comparison of electrophysiological substrate ablation in the left atrium during sinus rhythm and linear ablation based on circumferential pulmonary vein isolation in patients with long-standing persistent atrial fibrillation: a prospective randomized controlled study (Pilot study) (SINUS)

Comparison of electrophysiological substrate ablation in the left atrium during sinus rhythm and linear ablation based on circumferential pulmonary vein isolation in patients with long-standing persistent atrial fibrillation: a prospective randomized controlled study (Pilot study) (SINUS)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060005
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

long-standing persistent atrial fibrillation

Interventions

Experimental group:Circumpulmonary vein isolation (CVPI) and subsinusional stroma mapping for individualized ablation strategies
Control group:Circumferential pulmonary vein isolation + linear ablation

Sponsors

The First Affiliated Hospital with Nanjing Medical University (Jiangsu Province Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with symptomatic persistent atrial fibrillation who do not respond to treatment with at least one antiarrhythmic drug; 2. Aged 18-75 years; 3. Duration of atrial fibrillation >=1 year and less than 3 years; 4. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have previously received catheter ablation for atrial fibrillation; 2. Severe heart valve disease; 3. Severe structural heart disease; 4. Left atrial thrombosis; 5. Left atrial diameter (LAD) >55mm; 6. Platelet count 3 times the upper limit; Serum creatinine >3.5mg/dl or creatinine clearance <30ml/min); 10. Allergy to low molecular weight heparin, warfarin or new oral anticoagulants; 11. Life expectancy <1 year; 12. Pregnant and lactating patients.

Design outcomes

Primary

MeasureTime frame
Proportion of sinus rhythm maintenance within 1 year after operation;

Secondary

MeasureTime frame
Perioperative serious complications (pericardial tamponade requiring surgical intervention, atrial esophageal fistula, stroke, pulmonary vein stenosis);The percentage of intraoperative spontaneous sinus cardioversion;The proportion of all ablation lines reached complete bidirectional block;Proportion of atrial tachycardia within 1 year after operation;

Countries

China

Contacts

Public ContactZhang Fengxiang

The First Affiliated Hospital of Nanjing Medical University

njzfx6@163.com+86 13952037301

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026