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The Effect of High Dose Vitamin C in Burn Patients

NCT00350077 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2011-12-20

No results posted yet for this study

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.

Conditions

  • Burns

Interventions

DRUG

Intravenous Vitamin C

vitamin C IV during 24 hour period following burn

DRUG

Vitamin C

IV vitamin C

Sponsors & Collaborators

  • University of Miami

    collaborator OTHER

  • United States Army Institute of Surgical Research

    lead FED

Principal Investigators

  • Lorne H Blackbourne, MD · United States Army Institute of Surgical Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
72 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-07-31
Primary Completion
2008-03-31
Completion
2008-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00350077 on ClinicalTrials.gov