Efficacy Of Tocotrienol a Natural Vitamin E In Biopsy Wound
Status unconfirmed · Has a placebo group
Conditions studied: Scar
In brief
The following two objectives are proposed in healthy subjects to characterize (1) wound closure, (2) scar formation/appearance, and (3) inflammatory response: Objective 1, (topical only - referred to as "TOP") - Topical application of Tocotrienol (TCT) vs placebo in bilateral punch biopsy Objective 2, (oral and topical - referred to as "OTOP") - Combined oral supplementation and topical application of tocotrienol (TCT) vs placebo in bilateral punch biopsy Objective 3, (topical only - referred to as "TAM") - Topical application of tamoxifen vs placebo in bilateral punch biopsy. Objective 4, (topical only to normal skin) - Topical application of TCT vs placebo on bilateral lets on normal skin.
Key facts
- Study ID
- NCT01579227
- Run by
- Chandan K Sen
- People needed
- 101
- Starts
- 2012-01-01
- Expected to finish
- 2018-12-01
- Last updated by the study team
- 2018-01-29
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Ages- 18-50 (Both Male \& Female)
- Non-smoker - having quit at least 3 months prior to enrollment
- Non-diabetic
- Non-pregnant or non-breastfeeding - verbal assent.
- If a female subject of childbearing age misses her menstrual period after the start of the study, she will inform the investigators and be given a pregnancy test to ensure, for safety reasons, that she is not pregnant. If she is pregnant, she will discontinue participation in the study.
- No current use of OTC medications or other form of supplements containing vitamin-E
You may not qualify if…
- Diabetes or HIV diagnosis
- Alcohol or drug abuse
- unable to provide informed consent
- Therapeutically anti-coagulated
- Prisoner
- Currently prescribed immunosuppressant medication
Where it is running
- The Ohio State University Medical Center — Columbus, Ohio, United States
Full record on ClinicalTrials.gov
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