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Application of new intelligent management mode of warfarin anticoagulation in high-risk population of thromboembolic diseases

Application of new intelligent management mode of warfarin anticoagulation in high-risk population of thromboembolic diseases

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064330
Enrollment
Unknown
Registered
2022-10-02
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

thrombosis disease

Interventions

Test Group:POCT device was used to detect PT/INR at home, and anticoagulation management program was used for anticoagulation management
Control Group:The PT/INR was detected in the hospital, and the anticoagulation adjustment was guided by the doctor or clinical pharmacist according to the INR results.

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who need warfarin after artificial heart valve replacement, atrial fibrillation, cerebral infarction, venous thromboembolism, etc.; 2. Age 18 years or older, both sexes; 3. All patients and their family members signed informed consent voluntarily; 4. Warfarin was administered during the trial period.

Exclusion criteria

Exclusion criteria: 1. Patients with previous mental illness or cognitive, language and communication disorders; 2. Patients with malignant tumors and complicated with other anticoagulant and antiplatelet agglutination drugs; 3. Patients with other coagulation diseases; 4. Women preparing for pregnancy, pregnancy or lactation during the test cycle.

Design outcomes

Primary

MeasureTime frame
prothrombin time;prothrombin time;

Countries

China

Contacts

Public ContactLei Huang

Peking University Shenzhen Hospital

doctorlay@163.com+86 13728793009

Outcome results

None listed

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