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Effect of Low-dose vs Standard-dose Rivaroxaban Prophylaxis on Venous Thromboembolism Among Patients Undergoing Knee Arthroplasty: a Randomized Clinical Trial

Effect of Low-dose vs Standard-dose Rivaroxaban Prophylaxis on Venous Thromboembolism Among Patients Undergoing Knee Arthroplasty: a Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063471
Enrollment
Unknown
Registered
2022-09-07
Start date
2022-09-07
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Osteoarthritis

Interventions

A group:Rivaroxaban (5 mg po qd)
B group:Rivaroxaban (10 mg po qd)

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Primary unilateral total knee arthroplasty; 2. Aged 40-76 years male and female; 3. Patient should agree to joint the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patient who use aspirin for tertiary prevention or double antiplatelet therapy, including acute coronary syndrome in past 3 months, post-operation of PCI or cardiac valve replacement, and other high-risk patient; 2. Patient with high risk of VTE, including previous VTE history, malignant tumor, hypercoagulable state, other known states that easily lead to thrombosis and undergoing anticoagulation; 3. Patient with other severe disease in heart, brain, lung, kidney or blood; 4. Patient with coagulation dysfunction, trend of hemorrhage or has active hemorrhage before operation; 5. Patient with systematic artery stenosis or received stent implantation for such disease; 6. Patient with Severe renal insufficiency(Ccr 30).

Design outcomes

Primary

MeasureTime frame
Ultrasound of deep vein of lower extremity;post-operation symptomatic venous thromboembolism (VTE) event;bleeding event;total blood loss;poor healing of incisions;

Secondary

MeasureTime frame
traditional Coagulation Indicators;the incidence of subcutaneous ecchymosis;amount of blood transfusion;

Countries

China

Contacts

Public ContactShirong Chen

The Second Affiliated Hospital of Chongqing Medical University

chensr128@sohu.com+86 13883111390

Outcome results

None listed

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