effectivness of amantadine hydrocholoride on functional recovery in sever traumatic brain injery
Not Applicable
Recruiting
- Conditions
- evel of consciousness and cognitive function in patients with trauma.
- Registration Number
- IRCT20120527009878N7
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1- Patients aged 18 to 65 years
2. Those who have not had a known disease prior to head injury.
3. The supervisor will provide his written consent on his behalf
Exclusion Criteria
1-People with severe cardiovascular disease or congestive heart failure, myocardial infarction, persistent spinal cord injury, cancer, or any other severe disease that affects the evaluation of treatment.
2-People with chronic steroid therapy
3-Individuals received any other drug within 30 days of injury.
4-Significant TBI, brain tumor, cerebrovascular event, or other persistent brain illusions
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mini-mental Status Test (MMSE) scoring for patients with severe acute trauma. Timepoint: During surgery and duration of hospitalization after surgery. Method of measurement: Check out the Mini-mental Status Test (MMSE) table.;Disability Rating Scale (DRS) scoring for patients with severe acute traumatic brain injury. Timepoint: During surgery and duration of hospitalization after surgery. Method of measurement: Disability Rating Scale (DRS) Score.;Glasgow Outcome Scale Scoring (GOS) for patients with severe acute traumatic brain injury. Timepoint: During surgery and duration of hospitalization after surgery. Method of measurement: Check Glasgow Outcome Scale Table (GOS).
- Secondary Outcome Measures
Name Time Method