Skip to content

Application of rivaroxaban in the study of factors related to coagulation function in perioperative period of hip and knee replacement

Application of rivaroxaban in the study of factors related to coagulation function in perioperative period of hip and knee replacement

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021589
Enrollment
Unknown
Registered
2019-02-28
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-03-04

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

Conditions

Hip and knee replacement

Interventions

rivaroxaban group:Rivaroxaban was used for anticoagulation during perioperative period
low molecular heparin group:Low molecular weight heparin (LMWH) was used in perioperative anticoagulation

Sponsors

Department of Orthopaedics, First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) patients undergoing primary total hip and knee arthroplasty in our department; (2) Aged at least 18 years old; (3) preoperative color doppler ultrasound examination of DVT(-) in both lower limbs; (4) platelet count 100-300 X 10^9/L; (5) the postoperative application of rivaroxaban anticoagulation therapy; (6) patients' informed consent.

Exclusion criteria

Exclusion criteria: 1. preoperative color doppler examination of lower extremity DVT(+), or venous valve dysfunction of lower extremity; 2. have a history of lower limb venous thrombosis or pulmonary embolism; 3. preoperative coagulation dysfunction, contraindication of anticoagulation therapy, or high risk of bleeding (platelet count <100 X 10^9/ l-prothrombin activity <60%), or active bleeding, or taking anticoagulant drugs cannot be stopped; 4. revision surgery or surgical joint infection (specific or non-specific); 5. patients with contraindications specified in the directions of rivaroxaban: patients who are allergic to rivaroxaban or any excipients in the tablets; Liver disease patients with clinically relevant risk of bleeding; Pregnant and lactating women; 6. the patient refused to participate.

Design outcomes

Primary

MeasureTime frame
Determination of anti - factor Xa activity;thromboelastogram;Blood routine, liver and kidney function, blood coagulation;ecchymosis;

Countries

China

Contacts

Public ContactWei Huang

First Affiliated Hospital of Chongqing Medical University

weih68@hotmail.com+86 13883383330

Outcome results

None listed

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