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Clinical Trial Summary

The purpose of this study is to evaluate the 8-hour moisturization efficacy of OTC sunscreen lip balm after a single treatment application.


Clinical Trial Description

A single-center, randomized, controlled, intra-individual comparison, open label clinical study to determine the 8-hour moisturization efficacy of a sunscreen lip balm. Skin hydration will be assessed before (Baseline) and after (2, 4, 6 and 8 hours post-treatment) a single treatment with test product, compared to 'no treatment' as control, using a corneometer. Study treatments will be randomly assigned to 2 test sites delineated on the skin of the participant's volar forearms (one test site on each arm). A 1-week conditioning phase will precede the test day, during which participants will use the soap provided for personal washing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05109117
Study type Interventional
Source HALEON
Contact
Status Completed
Phase N/A
Start date December 7, 2021
Completion date December 17, 2021

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