Efficacy Evaluation of Avance QQ Collagen for Skin Beautification

April 9, 2025 updated by: TCI Co., Ltd.
To assess Avance QQ Collagen product on skin condition improvement

Study Overview

Study Type

Interventional

Enrollment (Actual)

75

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

      • Pingtung, Taiwan, 928
        • 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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy male or female adults, age above 18 years old;
  • The grade of crow's feet above 2 (Han et al. Sci Rep 13, 18903 (2023));
  • Commitment not to use products having activity comparable with that of the product to be tested during the study period;
  • Free of any dermatological or systemic disorder that would interfere with results.

Exclusion Criteria:

  • Subject with obvious skin surface damage;
  • Subject who had oral or topical medication which may affect skin condition within 1 month;
  • Subject who is a vegetarian or likely to be acutely allergic to the listed ingredients in the product;
  • Female who is pregnant, nursing or planning to become pregnant during the course of the study;
  • Received facial laser therapy, chemical peeling in the past 2 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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Placebo drink
consume 50 g liquid drink daily for 8 consecutive weeks
Active Comparator: Non-liposomal collagen drink
consume 50 g liquid drink daily for 8 consecutive weeks
Experimental: Liposomal collagen drink
consume 50 g liquid drink daily for 8 consecutive weeks
Other Names:
  • Avance QQ Collagen

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The change of skin elasticity
Time Frame: Change from Baseline skin elasticity at 8 weeks
Cutometer® MPA580 was utilized to measure skin elasticity. Units: arbitrary units
Change from Baseline skin elasticity at 8 weeks
The change of skin collagen density
Time Frame: Change from Baseline skin collagen density at 8 weeks
DermaLab® Series SkinLab Combo was utilized to measure skin collagen density. Units: arbitrary units
Change from Baseline skin collagen density at 8 weeks
The change of skin wrinkles
Time Frame: Change from Baseline skin wrinkles at 8 weeks
VISIA Complexion Analysis was utilized to measure skin wrinkles. Units: the amount of detectable wrinkles
Change from Baseline skin wrinkles at 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The change of wrinkles around the eyes
Time Frame: Change from Baseline wrinkles around the eyes at 8 weeks
VISIA Complexion Analysis was utilized to measure wrinkles around the eyes. Units: the amount of detectable wrinkles
Change from Baseline wrinkles around the eyes at 8 weeks
The change of skin hydration
Time Frame: Change from Baseline skin hydration at 8 weeks
Corneometer® CM825 (CK, Germany) was utilized to measure skin surface hydation. Units: arbitrary Corneometer® units 0-120.
Change from Baseline skin hydration at 8 weeks
The change of skin lightness
Time Frame: Change from Baseline skin lightness at 8 weeks
Chroma Meter MM500 was utilized to measure face skin lightness. Units: L* index
Change from Baseline skin lightness at 8 weeks
The change of skin tone
Time Frame: Change from Baseline skin tone at 8 weeks
Chroma Meter MM500 was utilized to measure face skin color. Units: Individual Typology Angle (ITA°)
Change from Baseline skin tone at 8 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
The change of self-assessment skin condition
Time Frame: Change from Baseline skin condition at 8 weeks
A self-assessment questionnaire was collected and evaluate skin condition.
Change from Baseline skin condition at 8 weeks

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: Chia-Hua Liang, Ph.D., Chia Nan University of Pharmacy & Science

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)

November 1, 2024

Primary Completion (Actual)

January 24, 2025

Study Completion (Actual)

February 28, 2025

Study Registration Dates

First Submitted

January 8, 2025

First Submitted That Met QC Criteria

January 8, 2025

First Posted (Actual)

January 13, 2025

Study Record Updates

Last Update Posted (Actual)

April 13, 2025

Last Update Submitted That Met QC Criteria

April 9, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 24-088-B

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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