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Effect of N-Acetylcysteine on moderate to severe traumatic brain injury patients

Not Applicable
Recruiting
Conditions
Injury, Occupational Diseases, Poisoning
Nervous System Diseases
Registration Number
PACTR202209548995270
Lead Sponsor
Faculty of Pharmacy Damanhour University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

1.Males or Females from 18 to 90 Years.
2.Hospital admission in the first 24 h of injury.
3.Moderate to severe traumatic brain injury (GCS score = 12)
4.The ability to tolerate enteral feeding.
5.Consenting guardian / relative.

Exclusion Criteria

1.Pregnant and breast-feeding women
2.Late presentation to hospital >24 hours.
3.Pre-existing hepatic failure.
4.Pre-existing renal failure.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
•Difference between the two groups in NSE levels on day 7
Secondary Outcome Measures
NameTimeMethod
•Difference between the two groups in S100B levels on day 7<br>•Difference between the two groups in MDA levels on day 7<br>•Difference between the two groups in IL-6 levels on day 7<br>•Glasgow coma scale (GCS)<br>
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