Hydrolyzed Collagen Combined With Djulis and Green Caviar Improve Skin Condition

January 12, 2021 updated by: TCI Co., Ltd.
Collagen combined with djulis and green caviar improve skin condition

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Using collagen drinks combined fish collagen with djulis, and green caviar to improve skin condition.

Study Type

Interventional

Enrollment (Actual)

50

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

  • Taiwan
      • Taipei, Taiwan
        • Research & Design Center, TCI CO., Ltd

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 to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Dry skin
  2. Rough skin
  3. Large pores
  4. Dark yellow complexion
  5. Sagging skin

Exclusion Criteria:

  1. Skin disorders
  2. Liver diseases
  3. Kidney diseases
  4. Allergy to cosmetics, drugs, or foods
  5. Pregnant and lactating women
  6. People who had any cosmetic procedures before 4 weeks of the study
  7. Area of facial spot over 3 cm2
  8. Vegan
  9. People who took collagen supplements in the past 3 months.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: placebo group
subjects drank 50 ml every night for 14, 28 days
Dietary supplement: placebo group
subjects drank 50 ml every night for 14, 28 days
Experimental: collagen drinks
subjects drank 50 ml every night for 14, 28 days
Dietary supplement: collagen drinkss
subjects drank 50 ml every night for 14, 28 days

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
skin moisture
Time Frame: subjects drank 50 ml every night for 28 days
using corneometer CM825 to examine skin moisture (The higher the value, the more water content, C.U., corneometer units )
subjects drank 50 ml every night for 28 days
skin elasticity
Time Frame: subjects drank 50 ml every night for 28 days
using cutometer dual MPA580 to examine skin elasticity (The closer the R2 value is to 1, the better the elasticity and no unit)
subjects drank 50 ml every night for 28 days
skin gloss
Time Frame: subjects drank 50 ml every night for 28 days
using probe system GL2000 & MPA10 to examine skin gloss (The higher the value, the higher the gloss, no unit)
subjects drank 50 ml every night for 28 days
skin spot
Time Frame: subjects drank 50 ml every night for 28 days
usig VISIA-CR to examine skin spot (The higher the value, the larger the pore area, mm2)
subjects drank 50 ml every night for 28 days
skin wrinkle
Time Frame: subjects drank 50 ml every night for 28 days
using VISIOSCAN-VC20 to examine skin wrinkle (The higher the value, the more wrinkles, surface evaluation of wrinkles, SEW)
subjects drank 50 ml every night for 28 days
skin roughness
Time Frame: subjects drank 50 ml every night for 28 days
using VISIOSCAN-VC98 to examine skin roughness (The higher the value, the higher the roughness, surface evaluation of roughness, SEr)
subjects drank 50 ml every night for 28 days
skin smoothness
Time Frame: subjects drank 50 ml every night for 28 days
using VISIOSCAN-VC98 to examine skin smoothness (The lower the value, the higher the smoothness, surface evaluation of smoothness, SEsm)
subjects drank 50 ml every night for 28 days

Collaborators and Investigators

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

Sponsor

TCI Co., Ltd.

Investigators

  • Principal Investigator: Chi Fu Chiang, Ph.D, Research & Design Center, TCI CO., Ltd

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)

May 1, 2020

Primary Completion (Actual)

June 30, 2020

Study Completion (Actual)

August 31, 2020

Study Registration Dates

First Submitted

January 11, 2021

First Submitted That Met QC Criteria

January 12, 2021

First Posted (Actual)

January 14, 2021

Study Record Updates

Last Update Posted (Actual)

January 14, 2021

Last Update Submitted That Met QC Criteria

January 12, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • EWISH-20190917-01

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.

Clinical Trials on Skin Condition

Clinical Trials on placebo group

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Venezuela

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe