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Effect of Vitamin D3 in patients with Traumatic Brain Injury

Phase 3
Conditions
Moderate to severe Traumatic brain injury.
Multiple injuries of head
S09.8
Registration Number
IRCT20180522039777N2
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
42
Inclusion Criteria

TBI patients with age range of 18 to 65 years GCS score between 3 and 12 TBI patients with vitamin D level less than 30 ng/ml

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum level of Interleukin-1-beta. Timepoint: The first day of study entry and 72 hours later. Method of measurement: Patient serum sample.
Secondary Outcome Measures
NameTimeMethod
eutrophil to lymphocyte ratio (NLR) and platelet to lymphocyte ratio (PLR). Timepoint: From the first day of sampling for 7 consecutive days. Method of measurement: Blood cell count.
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