Investigation of the Efficacies of a Resveratrol Formula on Improvement of Skin Conditions and Inflammatory Related Factors (Resveratrol)

January 13, 2021 updated by: TCI Co., Ltd.

Investigation of the Efficacies of a Resveratrol Formula on Improvement of Skin

To assess a resveratrol formula on improvement of skin conditions and inflammatory cytokines in blood

Study Overview

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Tainan City, Taiwan, 71710
        • Chia Nan University of Pharmacy & Science

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Healthy volunteers aged above 20 years old

Exclusion Criteria:

  • Subject who is not willing to participate in this study.
  • Patients with diseases of the skin, heart, liver, kidney, endocrine and other organs and patients with mental illness (according to medical history).
  • Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder.
  • Female who is pregnant or nursing or planning to become pregnant during the course of the study.
  • Received facial laser therapy, chemical peeling or UV overexposure in the past 4 weeks.
  • Subjects who have large spots (area >3 square centimeter) or abnormal acne.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Placebo drink
Subjects will consume a bottle of placebo drink for two months.
Experimental: Resveratrol drink
Subjects will consume a bottle of resveratrol drink for two months.
Other Names:
  • Grape Yeast Compound Fruit Vegetable Beverage

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The change of skin moisture
Time Frame: 0, 4, and 8 weeks
Corneometer® CM825 was utilized to measure skin moisture. Units: arbitrary Corneometer® units 0-120
0, 4, and 8 weeks
The change of skin elasticity
Time Frame: 0, 4, and 8 weeks
Cutometer® dual MPA 580 was utilized to measure skin elasticity (parameter R2). Units: μm penetration depth into the probe opening, expressed as curves
0, 4, and 8 weeks
The change of skin wrinkles
Time Frame: 0, 4, and 8 weeks
VISIA Complexion Analysis System was utilized to measure wrinkles. Units: arbitrary units
0, 4, and 8 weeks
The change of skin collagen density
Time Frame: 0, 4, and 8 weeks

DermaLab® USB - 20 MHz High Freq. Ultrasound probe was utilized to scan and analyze skin collagen density. Units:

Intensity score

0, 4, and 8 weeks
The change of skin texture
Time Frame: 0, 4, and 8 weeks
VISIA Complexion Analysis System was utilized to measure skin texture. Units: arbitrary units
0, 4, and 8 weeks
The change of skin pores
Time Frame: 0, 4, and 8 weeks
VISIA Complexion Analysis System was utilized to measure skin pores. Units: arbitrary units
0, 4, and 8 weeks
The change of total antioxidant capacity of blood
Time Frame: 0 and 8 weeks
Total Antioxidant Capacity Assay Kit
0 and 8 weeks
The change of TNF-alpha of blood
Time Frame: 0 and 8 weeks
ELISA Kit
0 and 8 weeks
The change of IL-6 of blood
Time Frame: 0 and 8 weeks
ELISA Kit
0 and 8 weeks
The change of IL-17 of blood
Time Frame: 0 and 8 weeks
ELISA Kit
0 and 8 weeks
The change of IL-1β of blood
Time Frame: 0 and 8 weeks
ELISA Kit
0 and 8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 17, 2020

Primary Completion (Actual)

November 10, 2020

Study Completion (Actual)

December 31, 2020

Study Registration Dates

First Submitted

June 30, 2020

First Submitted That Met QC Criteria

June 30, 2020

First Posted (Actual)

July 7, 2020

Study Record Updates

Last Update Posted (Actual)

January 15, 2021

Last Update Submitted That Met QC Criteria

January 13, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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