Could a common vitamin speed burn recovery?
NCT ID NCT01749371
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This trial investigates whether high-dose vitamin E (alpha-tocopherol) can reduce oxidative stress and improve outcomes in adults with severe burns covering at least 40% of their body. Participants receive vitamin E drops after surgery, and researchers measure vitamin levels, lung function, and markers of healing. The goal is to see if this simple supplement can lessen complications like lung injury and slow wound healing, potentially shortening hospital stays.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- vitamin E (alpha-tocopherol) given as oral drops
- What this could lead to
- If it works, this could lead to a simple, safe vitamin supplement that helps burn patients heal faster and spend less time in the hospital.
- What could go wrong
- This is a small, early-phase trial with only 27 participants, so results may not apply to all burn patients. High-dose vitamin E slightly increases bleeding risk.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
27 people
The number who actually took part.
- Started
-
Feb 2013
- Finished
-
Sep 2017
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
16 to 85 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age: 16 - 85 years * ≥40% total body surface area burn Exclusion Criteria: * Septic shock * Bleeding disorders * Diabetes, or on diabetes medications or anti-lipidemic agents * Arthritis * Known kidney/renal disease, endocrine disease, cancer, heart disease, osteoporosis, liver disease * Congestive heart failure * Positive hepatitis or HIV screens * Pregnancy (women)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Memorial Hermann Hospital Burn Intensive Care Unit
Houston, Texas, 77030, United States
-
University of Texas Medical Branch: Blocker Burn Unit and Shriners Hospitals for Children
Galveston, Texas, 77555, United States
-
University of Texas Southwestern Medical Center, Parkland Health and Hospital System
Dallas, Texas, 75390, United States
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