CTRI/2022/12/047966
Recruiting
Phase 3
A comparative study of the therapeutic efficacy of oral clonazepam and oral baclofen on spasms among patients with spinal cord injury: A randomised controlled trial.
Bharat Pulavarti0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: S140- Concussion and edema of cervical spinal cordHealth Condition 2: S340- Concussion and edema of lumbar andsacral spinal cordHealth Condition 3: S240- Concussion and edema of thoracic spinal cordHealth Condition 4: S141- Other and unspecified injuries ofcervical spinal cordHealth Condition 5: S241- Other and unspecified injuries ofthoracic spinal cordHealth Condition 6: S341- Other and unspecified injury of lumbar and sacral spinal cord
- Sponsor
- Bharat Pulavarti
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Spinal cord injury patients in the above age group, suffering from spasms, have sufficient mental capacity to respond relevantly to all queries related to spasms.
Exclusion Criteria
- •Spinal cord injury patients who exhibit spasticity but do not present with spasms.
- •Patients who are pregnant.
- •Patients with narrow angle glaucoma.
- •Patients with history of clinical depression and suicidal tendencies. Patients who are currently on antispastic and anti\-spasm medication will not be enrolled in the study.
- •Patients with deranged complete blood count, liver function tests and renal function tests.
- •Patients with pre\-existing musculoskeletal disorders and movement disorders in which spasms and spasticity cannot be assessed accurately.
Outcomes
Primary Outcomes
Not specified
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