Clinical Trials Directory

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

TypeNameDescription
DRUGApixabantreatment for 6 to 12 weeks
DRUGEnoxaparin Sodiumtreatment 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.