Efficacy Evaluation of Avance QQ Collagen for Skin Beautification

NCT ID: NCT06771388

Last Updated: 2025-04-13

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

75 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-01

Study Completion Date

2025-02-28

Brief Summary

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To assess Avance QQ Collagen product on skin condition improvement

Detailed Description

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Conditions

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Skin Condition Liposomal Encapsulation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Placebo drink

Group Type PLACEBO_COMPARATOR

Placebo drink

Intervention Type DIETARY_SUPPLEMENT

consume 50 g liquid drink daily for 8 consecutive weeks

Non-liposomal collagen drink

Group Type ACTIVE_COMPARATOR

Non-liposomal collagen drink

Intervention Type DIETARY_SUPPLEMENT

consume 50 g liquid drink daily for 8 consecutive weeks

Liposomal collagen drink

Group Type EXPERIMENTAL

Liposomal collagen drink

Intervention Type DIETARY_SUPPLEMENT

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

Intervention Type DIETARY_SUPPLEMENT

Non-liposomal collagen drink

consume 50 g liquid drink daily for 8 consecutive weeks

Intervention Type DIETARY_SUPPLEMENT

Placebo drink

consume 50 g liquid drink daily for 8 consecutive weeks

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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Avance QQ Collagen

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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TCI Co., Ltd.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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Taiwan

Other Identifiers

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24-088-B

Identifier Type: -

Identifier Source: org_study_id

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