NCT03487965

Evaluation of Skin Attributes Following Dietary Supplement Consumption

A Randomized, Double Blinded, Placebo Controlled Clinical Study to Evaluate Skin Attributes Following Dietary Supplement Consumption

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 103 (actual)
• Sponsor: Access Business Group · Industry
• Sex: Female
• Age: 30 Years – 65 Years
• Healthy volunteers: Accepted

Summary

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

Detailed 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.

Conditions

• Skin Condition

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	Low dose Polyphenol	botanical supplement with 25 mg polyphenol
DIETARY_SUPPLEMENT	High dose Polyphenol	botanical supplement with 13 mg polyphenol
DIETARY_SUPPLEMENT	Placebo Control	inert tablet made to mimic the experimental tablets

Timeline

• Start date: 2016-04-28
• Primary completion: 2017-06-28
• Completion: 2017-06-28
• First posted: 2018-04-04
• Last updated: 2018-04-06