Status:
WITHDRAWN
The Effect of High Dose Vitamin C in Burn Patients
Lead Sponsor:
United States Army Institute of Surgical Research
Collaborating Sponsors:
University of Miami
Conditions:
Burns
Eligibility:
All Genders
18-72 years
Phase:
NA
Brief Summary
The purpose of this study is to see if intravenous Vitamin C will decrease the amount of IV fluids needed following burn injury in the first 48 hours.
Detailed Description
Adequate fluid resuscitation in burn injured patients to allow adequate renal blood flow has been the hallmark of burn care in the last 50 years. The danger of exceeding the optimal intravenous fluid ...
Eligibility Criteria
Inclusion
- \>/= 20% total body surface area full and partial thickness burns
- Admitted to the USAISR burn center within 10 hours post injury
Exclusion
- Pregnant or breast feeding
- Documented preadmission or admission renal failure
- History of glucose-6-phosphate dehydrogenase deficiency, kidney stoves, gout or sickle cell
- Electrical injury
- Renal replacement of any kind\<24 hours after admission
Key Trial Info
Start Date :
July 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2008
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00350077
Start Date
July 1 2006
End Date
March 1 2008
Last Update
December 20 2011
Active Locations (1)
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1
United States Army Institute of Surgical Research
Fort Sam Houston, Texas, United States, 78234