Status:
TERMINATED
Antioxidant Supplementation in Trauma Patients
Lead Sponsor:
Boston Medical Center
Conditions:
Multiple Trauma
Eligibility:
All Genders
18-85 years
Phase:
PHASE3
Brief Summary
Administration of antioxidants to trauma patients will improve measures of oxidant stress in the blood
Eligibility Criteria
Inclusion
- Adult non pregnant non lactating trauma patient
Exclusion
- GCS \<6
- Renal dysfunction (cre \> 2.5 mg/dl)
- Hepatic dysfunction ( TBili \> 3.0 mg/dl)
- Expected survival \< 48 hours
- Burns over \> 20% body surface area
- Immune-deficiency syndromes
- Steroid use
Key Trial Info
Start Date :
November 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2009
Estimated Enrollment :
18 Patients enrolled
Trial Details
Trial ID
NCT00613392
Start Date
November 1 2007
End Date
November 1 2009
Last Update
January 26 2016
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