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RECRUITING
NCT07679945
NA

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

View on ClinicalTrials.gov

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

OTHER

Sunscreen untinted

Participants will apply the facial sunscreen on the face at least twice daily for 56 days

OTHER

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