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Safety and Efficacy of Non-Vitamin K Antagonist Oral Anticoagulants in Patients with Liver Disease: A Multicenter Cohort Study

Safety and Efficacy of Non-Vitamin K Antagonist Oral Anticoagulants in Patients with Liver Disease: A Multicenter Cohort Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108769
Enrollment
Unknown
Registered
2025-09-04
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Chronic liver disease patients requiring long-term regular anticoagulant therapy

Interventions

Control group:None
Study group:None

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Chinese male or female patients, age >= 18 years; 2. Long-term or regular anticoagulation therapy needs to be started; 3. Patients with chronic liver disease (Child-Pugh grade A/B/C) at the time of initiation of anticoagulation therapy; 4. Normal renal function or mild-moderate injury (eGFR >= 60 mL/min/1.73m^2).

Exclusion criteria

Exclusion criteria: 1.The initiation time of regular anticoagulant therapy is unknown; 2.Discontinuation of anticoagulant therapy within 1 month after initiation due to events such as bleeding/embolism; 3.Use of low-molecular-weight heparin for anticoagulant therapy; 4.Inability to obtain complete medical data.

Design outcomes

Primary

MeasureTime frame
Thromboembolic events;Bleeding events;

Secondary

MeasureTime frame
Compliance outcomes;

Countries

China

Contacts

Public ContactPengfei Jin

Beijing Hospital

j790101@163.com+86 10 85133620

Outcome results

None listed

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