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Summary
The goal of this clinical study is to evaluate the soothing effect of the test product within 2 hours after a single application by measuring changes in multiple indicators before and after product use. It will also assess the safety of the test product. The main questions it aims to answer are: * Does the test product relieve skin irritation and reduce skin redness within 2 hours after single use? * What adverse skin reactions do participants experience after using the test product? Researchers will compare the treated half-face with the untreated contralateral half-face (split-face control) to verify the soothing efficacy of the test product. Participants will: * Receive skin redness induction on both cheeks, then apply the test product on one side of the face * Undergo skin assessments at baseline before redness induction, post-induction, and at 10 seconds, 1 minute, 5 minutes, 10 minutes, 1 hour and 2 hours after product application * Complete clinical evaluation, instrumental measurement, image analysis and self-assessment questionnaires at each time point
Key Details
Gender
FEMALE
Age Range
25 Years - 45 Years
Study Type
INTERVENTIONAL
Enrollment
35
Start Date
2026-06-12
Completion Date
2026-06-30
Last Updated
2026-10-27
Healthy Volunteers
Yes
Interventions
Test soothing facial mask
Facial mask containing panthenol and madecassoside, applied on one hemiface for 15 minutes in single use after erythema induction.
Locations (1)
Shanghai China-norm Quality Technical Service Co., Ltd., Shanghai, Shanghai 200072, Shanghai,
Shanghai, Shanghai Municipality, China