Efficacy Evaluation of Avance QQ Collagen for Skin Beautification
NCT ID: NCT06771388
Last Updated: 2025-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
75 participants
INTERVENTIONAL
2024-11-01
2025-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
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Placebo drink
Placebo drink
consume 50 g liquid drink daily for 8 consecutive weeks
Non-liposomal collagen drink
Non-liposomal collagen drink
consume 50 g liquid drink daily for 8 consecutive weeks
Liposomal collagen drink
Liposomal collagen drink
consume 50 g liquid drink daily for 8 consecutive weeks
Interventions
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Liposomal collagen drink
consume 50 g liquid drink daily for 8 consecutive weeks
Non-liposomal collagen drink
consume 50 g liquid drink daily for 8 consecutive weeks
Placebo drink
consume 50 g liquid drink daily for 8 consecutive weeks
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 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 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.
18 Years
ALL
Yes
Sponsors
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TCI Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Chia-Hua Liang, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Chia Nan University of Pharmacy & Science
Locations
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Chia Nan University of Pharmacy & Science
Pingtung City, , Taiwan
Countries
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Other Identifiers
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24-088-B
Identifier Type: -
Identifier Source: org_study_id
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