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Pulmonary Vein Isolation With and Without Posterior Wall Isolation in Persistent Atrial Fibrillation

Randomized Controlled Study on the Efficacy and safety of Pulmonary Vein Isolation With and Without Posterior Wall Isolation in Persistent Atrial Fibrillation

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076635
Enrollment
Unknown
Registered
2023-10-13
Start date
2023-10-15
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Persistent Ayrial Fibrillation

Interventions

Pulmonary Vein Isolation Group:Pulmonary Vein Isolation
Pulmonary Vein Isolation(PVI) with Posterior Wall Isolation:PVI with Posterior Wall Isolation
electrophysiological test group:Atrial Fibrillation With a Left Atrial Low-Voltage Area underwent PVI+PWI
Atrial Fibrillation Without a Left Atrial Low-Voltage Area but ERP=180 ms underwent PVI+PWI
Atrial Fibrillation Without a Left Atrial Low-Voltage Area but ERP>180 ms underwent PVI.

Sponsors

The Second Hospital of Hebei Medical Uniesity.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Patients aged = 18 years old. ? Patients with persistent atrial fibrillation who comply with official guidelines,with a duration of atrial fibrillation of = 7 days and an electrocardiogram of atrial fibrillation. ? patients are able to sign an informed consent form and agree to participate in this study. ? Patients are able to comply with all research follow-up requirements.

Exclusion criteria

Exclusion criteria: ? Patients with valvular atrial fibrillation. ? The duration of atrial fibrillation is more than 3 years. ? Left atrial diameter = 45mm. ? With hypertrophic cardiomyopathy. ? Secondary atrial fibrillation caused by other diseases which can be corrected, such as hyperthyroidism. ? Those who have contraindications for using anticoagulants. ? Severe renal or liver failure.

Design outcomes

Primary

MeasureTime frame
The incidence of no atrial arrhythmias greater than 30 seconds;No use of antiarrhythmic drugs and no occurrence of atrial tachycardia/flutter exceeding 30 seconds;

Secondary

MeasureTime frame
No use of antiarrhythmic drugs and no occurrence of atrial fibrillation exceeding 30 seconds;Atrial fibrillation load;Ablation time and surgical time;Perioperative complications;

Countries

China

Contacts

Public ContactHao Jie

The Second Hospital of Hebei Medical Uniesity.

haojiemed@163.com+86 138 3310 0706

Outcome results

None listed

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