The Effect of High Dose Vitamin C in Burn Patients
Withdrawn before enrolling · Not applicable
Conditions studied: Burns
In brief
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.
Key facts
- Study ID
- NCT00350077
- Run by
- United States Army Institute of Surgical Research
- People needed
- 0
- Starts
- 2006-07-01
- Expected to finish
- 2008-03-01
- Last updated by the study team
- 2011-12-20
Who can join
Age: 18 and older, up to 72. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- >/= 20% total body surface area full and partial thickness burns
- Admitted to the USAISR burn center within 10 hours post injury
You may not qualify if…
- 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
Where it is running
- United States Army Institute of Surgical Research — Fort Sam Houston, Texas, United States
Full record on ClinicalTrials.gov
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