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Combined application of rivaroxaban and tranexamic acid in the management of hemorrhage and thrombosis in traumatic surgery

Combined application of rivaroxaban and tranexamic acid in the management of hemorrhage and thrombosis in traumatic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018927
Enrollment
Unknown
Registered
2018-10-17
Start date
2018-10-30
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Venous thromboembolism

Interventions

Control group:Physical prophylaxis Lower limb thrombosis
Tranexamic acid group:1g of intravenous tranexamic acid before incision, maintained at 15mg/kg during operation
Tranexamic acid + rivaroxaban group:1g of tranexamic acid before incision, maintained at 15mg/kg during operation, and rivaroxaban 8 hours after operation

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Adults older than 18 years of age; 2. Patients diagnosed with intertrochanteric fractures who require surgery; 3. Anesthesia risk rating scores ASA 1-3; 4. Willing to join the study and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with PE or DVT; 2. Patients with obvious liver disease (such as hepatitis B, hepatitis C, acute hepatitis, chronic active hepatitis, cirrhosis); 3. Creatinine clearance 180 mmHg or diastolic blood pressure > 110 mmHg; 6. may not be contraceptive measures may be pregnant, pregnant or lactating women; 7. need to apply CYP3A4 potent inhibitors; 8. acquired color vision Patients with disorders; 9. patients with thrombin; 10. patients with history of convulsions; 11. patients with atrial fibrillation with thrombophilia, patients after stent implantation, patients with cardiac pacemakers, etc.; 12. long-term oral antiplatelet drugs Patient; 13. long-term use of metformin patients.

Design outcomes

Primary

MeasureTime frame
bleeding volume during operation;bleeding volume after operation;Hemoglobin;D-dimer;Hematocrit;Prothrombin time;Activated partial thromboplastin time;Dual-leg vein ultrasound;

Countries

China

Contacts

Public ContactChen Yunzhen

Qilu Hospital of Shandong University

qilucyz@yeah.net+86 18560082566

Outcome results

None listed

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