Efficacy of Natural Vitamin E Tocotrienol on the Treatment of Surgical Scars

NCT00700791 · Status: TERMINATED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2021-11-18

No results posted yet for this study

Summary

The overall goal of this study is to determine the efficacy of tocotrienol (TCT), a natural form of vitamin E, in preventing or reducing scar formation in human skin wounds as well as the basal levels of TCT in normal human skin and adipose tissue.

Conditions

  • Scar

Interventions

DIETARY_SUPPLEMENT

Natural Vitamin E Tocotrienol supplement (TCT)

Oral Vitamin E Tocotrienol Supplement (TCT)

DEVICE

Natural Vitamin E Tocotrienol Cream (TCT)

Natural Vitamin E Tocotrienol(TCT)Topical Cream

OTHER

Placebo

Oral Placebo

OTHER

Placebo Cream

Topical Placebo Cream

Sponsors & Collaborators

  • Chandan K Sen

    lead OTHER

Principal Investigators

  • Chandan K Sen, PhD · Ohio State University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2018-07-31
Completion
2018-07-31

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 NCT00700791 on ClinicalTrials.gov