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COMPLETED
NCT01749371
PHASE2/PHASE3

Vitamin E Supplementation in Burned Patients

Sponsor: The University of Texas Medical Branch, Galveston

View on ClinicalTrials.gov

Summary

A dietary antioxidant, alpha-tocopherol, will be used to potentially attenuate Vitamin E short- and long-term losses in plasma and adipose, reverse the oxidative stress of burn injury and, in the process, decrease the secondary consequences of burn injury, including lung injury and impaired wound healing. This may improve the quality of life of the burn patient by preventing pathophysiology that may result from oxidative stress and may reduce hospital stay. Our research will lay the foundation for the future development of effective, safe, and economic therapeutic interventions to treat burn injury-associated metabolic abnormalities. Also, it will provide the basis for the development of supplemental regulations and pharmacotherapy to treat burn patients with vitamin E. The risks are very reasonable in relation to the anticipated benefits to our subjects because a) vitamin E is a simple vitamin that is abundant and approved for clinical use, and b) the subjects will be monitored consistently for the minimal increased tendency to bleed.

Key Details

Gender

All

Age Range

16 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

27

Start Date

2013-02

Completion Date

2017-09

Last Updated

2026-07-20

Healthy Volunteers

No

Conditions

Interventions

DRUG

Vitamin E

1200 IU dl-alpha tocopheryl acetate after the initial excision surgery after admission (days 1-15 or days 16-30)

Locations (3)

University of Texas Southwestern Medical Center, Parkland Health and Hospital System

Dallas, Texas, United States

University of Texas Medical Branch: Blocker Burn Unit and Shriners Hospitals for Children

Galveston, Texas, United States

Memorial Hermann Hospital Burn Intensive Care Unit

Houston, Texas, United States