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Comprehensive clinical evaluation of drugs

Comprehensive clinical evaluation of drugs

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110807
Enrollment
Unknown
Registered
2025-10-21
Start date
2023-10-08
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Nonvalvular atrial fibrillation, deep vein thrombosis, and pulmonary embolism

Interventions

Rivaroxaban anticoagulation therapy Observation group:None

Sponsors

The First Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult patients (aged >=18 years) who were admitted to hospital due to diagnosis of deep vein thrombosis, pulmonary embolism and non-valvular atrial fibrillation from January 2022 to October 2023 received rivaroxaban anticoagulation therapy during hospitalization or after discharge

Exclusion criteria

Exclusion criteria: 1.Patients with poor medication compliance, who fail to take their medication correctly as prescribed by the doctor or stop taking it at will; 2. Patients lost to follow-up; 3. Patients who alternate between domestic and original rivaroxaban.

Design outcomes

Primary

MeasureTime frame
Incidence of stroke/thromboembolism;Incidence of bleeding;

Secondary

MeasureTime frame
Coagulation indexes;

Countries

China

Contacts

Public ContactWei Yuhui

The First Hospital of Lanzhou University

yhwei@lzu.edu.cn+86 931 835 6854

Outcome results

None listed

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