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Comparison of efficacy and safety of one-stop treatment of atrial fibrillation with rivaroxaban and warfarin and study on antithrombotic therapy after one-stop operation

Comparison of efficacy and safety of one-stop treatment of atrial fibrillation with rivaroxaban and warfarin and study on antithrombotic therapy after one-stop operation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039907
Enrollment
Unknown
Registered
2020-11-14
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Auricular fibrillation

Interventions

One-stop therapy group:radiofrequency ablation and left atrial appendage closure
warfarin anticoagulant group:warfarin Oral
Levashaban anticoagulant group:Levashaban oral
Postoperative oral warfarin group:oral warfarin after operative
Postoperative oral rivastaben group:oral rivastaben after operative
Postoperative oral dabigatran group:oral dabigatran after operative

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with paroxysmal, persistent or permanent nonvalvular atrial fibrillation aged 18 or above; 2. Patients with high risk of stroke with cha2ds2 VASC score >= 2.

Exclusion criteria

Exclusion criteria: 1. Patients with warfarin contraindications; 2. Patients with complications other than atrial fibrillation requiring long-term warfarin treatment; 3. Patients with La or LAA thrombosis; 4. Atrial septal aneurysm with patent foramen ovale and right to left shunt; 5. Patients with aortic atherosclerosis and symptomatic carotid artery disease; 6. Patients with valvular diseases with indications for operation; 7. Patients with clinically significant bleeding, stroke or cardiac embolism within 30 days before operation; 8. Patients with ACS within 90 days before operation.

Design outcomes

Primary

MeasureTime frame
Ischemic events;Bleeding incidents;

Countries

China

Contacts

Public ContactShanglang Cai

Affiliated Hospital of Qingdao University

xclky9706@163.com+86 18661605505

Outcome results

None listed

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