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A Clinical Study to Evaluate the Efficacy in Improving Dark Spots After 8 Weeks of Use of Facial Sunscreens in Adult Participants
Sponsor: Kenvue Brands LLC
Summary
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.
Official title: A Monocentric and Open-Label Clinical Study to Evaluate the Efficacy in Improving Dark Spots After 8 Weeks of Use of Facial Sunscreens in Adult Research Participants
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
152
Start Date
2026-06-02
Completion Date
2026-09-25
Last Updated
2026-07-01
Healthy Volunteers
Yes
Interventions
Sunscreen untinted
Participants will apply the facial sunscreen on the face at least twice daily for 56 days
Sunscreen tinted
Participants will apply the facial sunscreen on the face at least twice daily for 56 days
Locations (1)
ALS Beauty & Personal Care Ltda
Campinas, São Paulo, Brazil