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Evaluation of Skin Attributes Following Dietary Supplement Consumption

NCT03487965 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 103

Last updated 2018-04-06

No results posted yet for this study

Summary

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

Conditions

  • Skin Condition

Interventions

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

Sponsors & Collaborators

  • Clinical Research Laboratories

    collaborator UNKNOWN

  • Access Business Group

    lead INDUSTRY

Principal Investigators

  • Anita L Cham, MD · Clinical Research Laboraties, LLC

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-04-28
Primary Completion
2017-06-28
Completion
2017-06-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03487965 on ClinicalTrials.gov