- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06771388
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
Status
Completed
Conditions
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:
|
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
Keywords
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.
Clinical Trials on Skin Condition
-
Finzelberg GmbH & Co. KGEurofins; Eurofins Dermscan PharmascanRecruitingSkin Condition | Skin Aging | Hair ConditionPoland
-
Indiana UniversityCompletedHypertrophic Skin Condition of Anterior AbdomenUnited States
-
Roswell Park Cancer InstituteNational Cancer Institute (NCI)TerminatedPrecancerous/Nonmalignant ConditionUnited States
-
TCI Co., Ltd.Recruiting
-
TCI Co., Ltd.Completed
-
Assiut UniversityNot yet recruiting
-
TCI Co., Ltd.Completed
-
Shanghai EGT Synbio Group Co., Ltd.Completed
-
TCI Co., Ltd.Completed
Clinical Trials on Placebo drink
-
Virginia Polytechnic Institute and State UniversityCompletedCardiovascular Risk FactorUnited States
-
University of California, RiversideA1CantusNot yet recruiting
-
University of the PacificCompletedCardiovascular DiseasesUnited States
-
Maastricht University Medical CenterTop Institute Food and NutritionCompletedMuscle Loss in ElderlyNetherlands
-
Wageningen UniversityMaastricht University Medical Center; Top Institute Food and NutritionCompleted
-
Mayo ClinicCompletedCardiovascular System | Hemodynamics | Energy DrinksUnited States
-
University of LimerickCompleted
-
University of LeedsArla FoodsCompletedCognitive Performance (Focus)United Kingdom