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COMPLETED
NCT07896993
NA

Mask Instant Clinical Study

Sponsor: ChinaNorm

View on ClinicalTrials.gov

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

OTHER

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