Clinical Trials Directory

Trials / Completed

CompletedNCT01640028

Exploratory Study of Intra and Inter-subject Variability in Sebum Excretion Rate

Status
Completed
Phase
Study type
Observational
Enrollment
41 (actual)
Sponsor
Innovaderm Research Inc. · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to analyze the relationship between sebum excretion rate and the following factors: * Hormone levels (testosterone, dehydroepiandrosterone sulfate) * Expression of 5-α-reductase type 1 (a protein in sebaceous glands that transforms a hormone (testosterone) into another one that strongly stimulates sebum production) * Diet * Sun and ultraviolet light exposure. * Facial washing routine * Sleep patterns (time when you start sleeping and total sleep time) This study will analyze the relationship between sebum excretion rate and the various factors that may influence it in approximately 40 subjects. It will be conducted in one center located in Montreal. All devices are known and have already been used in the past.

Detailed description

A total of 40 subjects with a sebum excretion rate of at least 4 will be included. Subjects will be seen at Day 0 and Day 7. Casual sebum measurements will be performed at least 2 hours after washing the face in the morning with a Sebumeter® following a 30-second application of a Sebumeter® Measurement Cartridge to the forehead. Sebum excretion rates will be measured with Sebutape® applied to the right and left forehead at each visit. Each Sebutape® will be scanned and the area covered by sebum, seen as gray-black dots on the scanned Sebutape®, will be measured by an image analysis software. Circulating levels of free testosterone and DHEAS will be measured at each visit. A skin biopsy behind an ear will be performed at Day 0 and Day 7 to measure gene expression of the 5-α-reductase type 1. On Day 0 and Day 7, subjects will be required to take a 24-hour recall questionnaire. On Day 0 and Day 7, subjects will be questioned about the time of sleep induction, their total sleep time for the night preceding the visit, facial washing routine and the number of hours of direct and indirect UV exposure in the past 24 hours. On Day 0 and Day 7, subject's forehead skin temperature will be measured.

Conditions

Timeline

Start date
2012-07-01
Primary completion
2012-09-01
Completion
2012-12-01
First posted
2012-07-13
Last updated
2017-03-10

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01640028. Inclusion in this directory is not an endorsement.