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Antioxidant Supplementation in Trauma Patients

NCT00613392 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2016-01-26

No results posted yet for this study

Summary

Administration of antioxidants to trauma patients will improve measures of oxidant stress in the blood

Conditions

  • Multiple Trauma

Interventions

DIETARY_SUPPLEMENT

powdered antioxidant

one vial mixed with water every day orally or through enteral tube

DIETARY_SUPPLEMENT

powdered cornstarch placebo

one vial mix with water and administer orally or via enteral tube

Sponsors & Collaborators

  • Boston Medical Center

    lead OTHER

Principal Investigators

  • Peter Burke, MD · Boston Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2009-11-30
Completion
2009-11-30

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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 NCT00613392 on ClinicalTrials.gov