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ASPIRIN discontinuation after left atrial appendage occlusion in atrial fibrillation: a double-blind, placebo-controlled randomized clinical trial

ASPIRIN discontinuation after left atrial appendage occlusion in atrial fibrillation: a double-blind, placebo-controlled randomized clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045649
Enrollment
Unknown
Registered
2021-04-20
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-06

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

Conditions

Atrial fibrillation

Interventions

Placebo group:Aspirin discontinuation

Sponsors

Xinhua Hospital Affiliated to Shanghai Jiaotong University of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients with nonvalvular atrial fibrillation had undergone left atrial appendage occlusion 6 months ago, including one-stop left atrial appendage occlusion + radiofrequency ablation; 2. Aged 18 to 90 years; 3. Provide informed consent to participate in the study, follow-up trials and assessment procedures.

Exclusion criteria

Exclusion criteria: 1. Patients with coronary heart disease, stroke and other diseases need to take aspirin for a long time for secondary prevention; 2. Existence of acute disease, such as acute phase after myocardial infarction (within 3 months), acute onset of heart failure or new cerebral infarction within 3 months; 3. Life expectancy is less than 1 year; 4. Contraindications to the use of aspirin such as active peptic ulcer or other bleeding diseases; 5. Patients with uncontrolled malignant tumors; 6. Obviously abnormal liver and kidney function and coagulation function; 7. Transesophageal echocardiography within 6 months after surgery showed thrombosis in the heart cavity, device-related thrombosis or residual leakage > 5mm; 8. Women who are pregnant, breastfeeding, planning to become pregnant, or women of childbearing age who have not adopted reliable contraceptive methods.

Design outcomes

Primary

MeasureTime frame
POCO composite endpoint;

Countries

China

Contacts

Public ContactLi Yigang

Xinhua Hospital Affiliated to Shanghai Jiaotong University of Medicine

153814599@qq.com+86 13761318166

Outcome results

None listed

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