Trials / Recruiting
RecruitingNCT05484557
Prevention of Thromboembolism Using Apixaban vs Enoxaparin Following Spinal Cord Injury
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Loewenstein Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Currently, Enoxaparin is the usual prophylactic anticoagulant treatment at the acute and sub-acute phases of spinal cord injury (SCI). Patients at the sub-acute phase of SCI (rehabilitation) will be given either Enoxaparin 40 mg/day (control) or Apixaban 2.5-5 mg twice a day. Apixaban dose will be determined by the treating physician. Treatment will be continued for either 6 or 12 weeks following injury (for AIS grades C-D and A-B respectively). Endpoints: Venous thromboembolism will be evaluated by D-Dimer test every 2 weeks and an ultrasound doppler at the beginning and the end of the treatment. Bleeding events will be recorded and hematocrit will be monitored every two weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Apixaban | treatment for 6 to 12 weeks |
| DRUG | Enoxaparin Sodium | treatment for 6 to 12 weeks |
Timeline
- Start date
- 2023-09-06
- Primary completion
- 2025-08-01
- Completion
- 2026-02-01
- First posted
- 2022-08-02
- Last updated
- 2025-05-09
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT05484557. Inclusion in this directory is not an endorsement.