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Effect and efficacy of aspirin or rivaroxaban on venous thrombosis in patients undergoing lumbar surgery

Effect and efficacy of aspirin or rivaroxaban on venous thrombosis in patients undergoing lumbar surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093611
Enrollment
Unknown
Registered
2024-12-09
Start date
2024-12-09
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Perioperative venous thromboembolic disease during lumbar spine surgery

Interventions

No Drug Prevention Group (blank control group):Basic Prevention+physical prevention+no drug prevention
Drug Prevention Group (aspirin group):Basic Prevention + Physical Prevention + Aspirin 100 mg/d x 14 days
Drug Prevention Group (Intervention Group 2: Rivaroxaban Group):Basic Prevention + Physical Prevention + rivaroxaban 10 mg/d x 14 days

Sponsors

the Seventh Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. 2024 10- 2026 09 Lumbar admitted. 2. Aged 18 to 80;

Exclusion criteria

Exclusion criteria: 1. Age under 18 or over 80; 2. Patients receiving preoperative anticoagulation therapy and patients with medical contraindications to both study drugs; 3. Except for patients with cancer 4. Except for patients for whom no prophylaxis is recommended. 5. Except for patients with an existing bleeding event. 6. Postoperative use of a variety of thromboprophylaxis in patients.

Design outcomes

Primary

MeasureTime frame
The incidence of VTE within 30 days after operation;

Secondary

MeasureTime frame
Cumulative incidence of VTE within 90 days;Bleeding events within 30 days and 90 days after discharge;Major risk factors for VTE;

Countries

China

Contacts

Public ContactFuxin Wei

The Seventh Affiliated Hospital of Sun Yat sen University (Shenzhen)

weifuxin@mail.sysu.edu.cn+86 135 6017 0686

Outcome results

None listed

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