The efficacy of fingolimod in enhancing recovery after traumatic spinal cord injury

Phase 2

Recruiting

• Conditions: spinal cord injury.; Injury, poisoning and certain other consequences of external causes; T09.3

• Registration Number: IRCT20240701062291N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 26 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 36

Inclusion Criteria

stable hemodynamic status
age between 20 and 60
Patients with acute traumatic spinal cord injury who referred within the first 8 hours

Exclusion Criteria

acute non traumatic spinal cord injury
Acute spinal cord injury that has been more than 8 hours since the trauma
Spinal cord injuries caused by firearms or cold weapons

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sensorimotor status of patients. Timepoint: Sensory and motor condition of patients are evaluated based on clinical examination immediately after administration (Before the intervention begins) and then at intervals of one month, three months, six months and one year after the intervention. Method of measurement: the sensory-motor condition of patients are evaluated based on American Spinal Injury Association Impairment Scale (AISA).;Sphincter function. Timepoint: administration and evaluation at intervals of six months and one year. Method of measurement: clinical examination and urodynamic study.