A trial of neuroprotective vitamin D in traumatic brain injury patients
Phase 3
- Conditions
- Cerebral trauma.Intracranial injury
- Registration Number
- IRCT20191026045243N2
- Lead Sponsor
- Sari University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 84
Inclusion Criteria
All patients admitted to the emergency department and then transferred to the neurosurgery ward
All patients admitted to the emergency department and then transferred to the ICU ward
Exclusion Criteria
Patients with brain death
Equal degree of vigilance
Patients hospitalized for less than 5 days
Penetrating brain injuries
Accompanying severe lesions
Severe lesions other than brain injuries such as hemothorax or hemo-peritoneum or any injury requiring rapid surgery and no opportunity for neurological examination in the early stages.
itamin D deficiency according to the standard amount reported. And less than 30 ng and more than 60 ng / ml
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of consciousness. Timepoint: Baseline and 7 and 90 days. Method of measurement: Glasgow level of consciousness.
- Secondary Outcome Measures
Name Time Method