A Clinical Study to Evaluate the Efficacy in Improving Dark Spots After 8 Weeks of Use of Facial Sunscreens in Adult Participants

Recruiting N/A Interventional Study
Post-inflammatory Hyperpigmentation Melasma Solar Lentigo
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
152 (estimated)
Sponsor
Kenvue Brands LLC · Industry
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About This Trial

The study aims to evaluate the efficacy of a facial sunscreen under two experimental conditions-untinted and tinted-in improving facial spots (melasma and solar lentigines/post-inflammatory hyperpigmentation) after 8 weeks of product use under normal conditions by adult participants.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Able to understand and follow study instructions 2. Fitzpatrick skin types I-VI 3. Presence of facial hyperpigmentation, such as: * Mild to moderate melasma, or * Visible dark spots (e.g., solar lentigines or post-inflammatory hyperpigmentation) 4. Willing to comply wi…
Contacts

Kenvue Global Clinical Operations

18779295131

KenvueClinical_KV@kenvue.com

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