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

NCT ID: NCT01640028

Last Updated: 2017-03-10

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 41 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2012-07-31
• Study Completion Date: 2012-12-31

Brief 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

Oily Skin

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

1. Subject has a sebum excretion rate of at least 4 at Day 0 on both sides of the forehead as measured with Sebutape.

2. Subject is 18 years of age or older at time of consent and is in generally good health.

3. Female subject is willing to use effective contraceptive method for at least 30 days before Day 0 and until the end of the study. Effective contraceptive methods are:

1. Barrier methods such as condom, sponge or diaphragm combined with spermicide in foam, gel or cream;

2. Hormonal contraception (oral, intramuscular, implant or transdermal) which include Depo-Provera, Evra and Nuvaring;

3. Intrauterine device (IUD);

4. Sterilization such as tubal ligation, oophorectomy, hysterectomy or vasectomized partner;

5. Postmenopausal state for at least 1 year for female subject or female partner of male subject;

6. Same-sex partner;

7. Abstinence.

4. Subject has a negative urine pregnancy test at Day 0 visit for female subject of childbearing potential only.

5. Subject is capable of giving informed consent and the consent must be obtained prior to any study related procedures.

Exclusion Criteria

1. Subject is currently pregnant or lactating.

2. Subject has any skin condition on the forehead that could interfere with sebum excretion measurement except for mild acne vulgaris.

3. Subject has received investigational drugs within the 28 days or 5 half-lives, whichever is longer, prior to Day 0 or plans to during the study period.

4. Subject has used any topical medication on the face within 14 days of Day 0 or plans to during the study.

5. Subject has applied cosmetics or emollients on the forehead the morning of Day 0 visit or plans to the morning of Day 7 visit.

6. At the investigator's discretion subject has current or history of alcohol or drug abuse that would interfere with the ability of the subject to comply with the study protocol.

7. Subject has used isotretinoin in the 52 weeks preceding Day 0 or plans to during the study.

8. Subject should not have swum in chlorinated water within 24 hours of the Day 0 visit or plans to within 24 hours of the Day 7 visit.

9. Known hypersensitivity/allergy to lidocaine

10. The subject has a history of keloids

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Innovaderm Research Inc.

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Robert Bissonnette, MD, FRCPC

Role: PRINCIPAL_INVESTIGATOR

Innovaderm Research

Locations

Innovaderm Research

Montreal, Quebec, Canada

Countries

Canada

Other Identifiers

Inno-6026

Identifier Type: -

Identifier Source: org_study_id