Efficacy Determination of Facial Anti-wrinkle Product Aging Solution Anti-wrinkle serum

Phase 1

Completed

• Conditions: Healthy Thai female subjects; anti-wrinkle

• Registration Number: TCTR20211208004
• Lead Sponsor: Aging Solution Co., Ltd.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-09-25
• Study Start: 2021-12-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 32

Inclusion Criteria

1. Healthy female aged between 30-60 years old
2. Be able to read, communicate and write Thai language
3. All skin types
4. Having clearly visible wrinkle at both eye corners
5. Having experience using a counter brand facial skin care
6. No allergic history to any ingredient in commercially available anti-wrinkle products or any cosmetics in the market
7. No history of changing any facial product/ food supplement at least 1 month before enrollment in this study
8. Voluntarily sign the consent form for the study after being informed about objective, methods, risks, product effects, and the other effects on the subjects (volunteers can inquire about further information related to the study that do not related to the trade secret of the product).

Exclusion Criteria

1. Having history of eczema or psoriasis within 6 months before enrollment in this study
2. Having wound and scar around the study-evaluating face area
3. Having history of using steroid, antibiotic, non-steroidal anti-inflammatory or antihistamine within 3 days before enrollment in this study
4. Having history of using topical medicine on face within 3 weeks before enrollment in this study
5. Having underlying disease and continuous taking medicine
6. Having history of major operation within 1 year
7. Having history of skin cancer within 1 year
8. Having pregnancy or lactation
9. Having history of regular smoking or regular drinking
10. Having history of participating in other clinical study within 3 months before enrollment in this study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Skin roughness and wrinkles 8 weeks The photographed of wrinkle area by Primos CR,Skin moisture 8 weeks Measuring by Corneometer,Skin elasticity 8 weeks Measuring by Cutometer

Secondary Outcome Measures

Name	Time	Method
/A N/A N/A