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Efficacy Evaluation Study of Vitamin C and Glutathione Liquid Sachet

Efficacy Evaluation Study of Vitamin C and Glutathione Liquid Sachet

Recruiting
18-65 years
All
Phase N/A

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Overview

The objective of this study is to evaluate the effect of liquid vitamin C and glutathione supplements on human skin condition improvement and anti-oxidation.

Description

This study is a single-center, placebo-controlled, double-blinded, parallel human trial designed to evaluate the skin beauty and anti-oxidant effect of liquid vitamin C and glutathione supplements.

Healthy adult participants aged 18-65 years will be enrolled. Participants will be informed to consume test samples daily for 12 consecutive weeks. Skin measurement and self-assessment questionnaires will be conducted at baseline (before intake), after 4, 8 weeks, and 12 weeks of consumption. Fasting blood samples will be collected at baseline and after 12 weeks of consumption.

Eligibility

Inclusion Criteria:

  • Healthy male or female adults, aged 18-65 years old;
  • 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 details
    Skin Condition
    Anti-Oxidative Stress

NCT07379216

TCI Co., Ltd.

31 January 2026

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