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Study on different anticoagulant course of isolated intermuscular venous thrombosis of calf after major orthopaedic surgery

Study on different anticoagulant course of isolated intermuscular venous thrombosis of calf after major orthopaedic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073445
Enrollment
Unknown
Registered
2023-07-11
Start date
2023-07-12
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Intermuscular vein thrombosis

Interventions

6-weeks anticoagulant group:After diagnosis of MCVT, oral rivaroxaban 10 mg/time, QD until discharge
after discharge, oral rivaroxaban tablets 10 mg/time, QD, anticoagulant treatment until 6 weeks
3-months anticoagulant group:After diagnosis of MCVT, oral rivaroxaban 10 mg/time, QD until discharge
after discharge, oral rivaroxaban tablets 10 mg/time, QD, anticoagulant treatment until 3 months

Sponsors

The Second Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients who received major orthopaedic surgery in our hospital from March 2023 to March 2025 were selected. 1. Body weight 50-100 kg; 2. No abnormal coagulation system and no history of thrombosis; 3. Patients who adopt standard major orthopedic surgery procedures and rehabilitation procedures; 4. Patients with fresh isolated distal calf intermuscular vein thrombosis confirmed by postoperative color ultrasound of lower extremity deep vein; 5. The routine anticoagulant regimen for VTE prevention was adopted in the perioperative period: anticoagulant drugs were stopped 12 h before surgery, and enoxaparin sodium 4,000 Axaiu/time was given 12-24 h after surgery, QD; 6. Voluntary participation and cooperation in the completion of this study.

Exclusion criteria

Exclusion criteria: 1. Preoperative ultrasonography showed the presence of thrombus in the lower extremities; 2. Cancer patients; 3. Patients who are at risk of severe bleeding and cannot receive ordinary anticoagulant therapy (active bleeding, recent hemorrhagic stroke or upper gastrointestinal bleeding, etc.); 4. Restricted activity affected the outcome of thrombus; 5. Combined with thrombosis in other parts (central deep vein thrombosis of lower extremity or combined with pulmonary embolism); 6. A wide range of involvement (more than 5 cm in length, multiple veins involved or a maximum diameter of more than 7 mm); 7. Antiphospholipid syndrome or symptomatic hereditary propensity to thrombosis; 8. pregnancy; 9. Use birth control pills or hormone replacement therapy.

Design outcomes

Primary

MeasureTime frame
Changes of intermuscular vein thrombosis;

Countries

China

Contacts

Public ContactZhu Zhu

The Second Affiliated Hospital of Soochow University

wwdz_@126.com+86 136 4621 3382

Outcome results

None listed

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