Evaluation of Skin Attributes Following Dietary Supplement Consumption

Status Completed

Clinical Trial Summary

The study is to assess skin attributes of female subjects following 16 weeks of dietary supplement consumption.

Clinical Trial Description

This is a 16 week, randomized, double blind, placebo controlled study. Approximately 105 Caucasian and Asian (Korean, Japanese, or Chinese) female subjects will be enrolled. The following clinical assessments will be performed: (1)VISIA-CR™ digital photography; (2)AGE Reader SU measurements on the left cheek and left inner forearm; (3) Visual Analog Grading (VAS); (4) Corneometer measurements; and (5) Cutometer measurements. Subjects will return to the clinic at approximately 4 weeks, 8 weeks and 16 weeks from the baseline visit for similar measurements. A self-perception questionnaire will be administered at the conclusion of the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03487965
Study type	Interventional
Source	Access Business Group
Contact
Status	Completed
Phase	N/A
Start date	April 28, 2016
Completion date	June 28, 2017

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