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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00884936
Other study ID # ILI-08-112-USKAG
Secondary ID
Status Completed
Phase N/A
First received April 20, 2009
Last updated March 30, 2015
Start date August 2008
Est. completion date April 2009

Study information

Verified date October 2009
Source Interleukin Genetics, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug AdministrationJapan: Institutional Review BoardJapan: Ministry of Health, Labor and Welfare
Study type Observational

Clinical Trial Summary

This study is a blinded, prospective, single-center, clinical study conducted in Japanese female subjects between the ages of 20-75 years. This design uses skin biopsy samples from environmentally exposed areas and unexposed (control) areas within the same subjects to assess the gene expression profile from three different age groups.


Description:

The primary objective of the skin aging study is to investigate changes in gene expression patterns that occur during the aging process.


Recruitment information / eligibility

Status Completed
Enrollment 121
Est. completion date April 2009
Est. primary completion date November 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- Individuals who are willing to read and sign an informed consent form prior to participating in the study.

- Individuals who have a temperature of less than or equal to 100 degrees F at the time of biopsy collection.

- Individuals who had not applied any sunless tanning product on the arms within the past year.

- Individuals with no prior history of alcoholism (or who consume fewer than 2 to 3 alcoholic beverages per day).

- Individuals who have not consumed any anti-aging nutritional supplements (multivitamins and multiminerals are acceptable) or aspirin, NSAIDS, or other pain medication in the last 48 hours before biopsy.

Exclusion Criteria:

- Male gender

- Individuals who did not fit the 'inclusion criteria' above.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Japan Thomas J. Stephens & Associates, Japan Research Center Tokyo

Sponsors (1)

Lead Sponsor Collaborator
Interleukin Genetics, Inc.

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary objective of the study is to investigate changes in gene expression patterns that occur during the aging process. A significant fold change in differential gene expression will be >1.5 and an adjusted p-value of <0.05. 1 year No
Secondary Secondary outcome measures are the evaluation of genetic expression changes in sun-protected and sun-exposed skin and an investigation of their biological pathways. 1 year No
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