Clinical Trials Directory

Trials / Completed

CompletedNCT02977507

Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topical Products in Participants With Moderate Facial Melasma

Randomized, Double-blinded, Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topical Products in Subjects With Moderate Facial Melasma

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Allergan · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to evaluate the efficacy and tolerability of Lytera 2.0 versus 4% hydroquinone in the improvement of the appearance of moderate facial melasma.

Conditions

Interventions

TypeNameDescription
OTHERLytera 2.0Lytera 2.0 applied to the affected areas twice a day, in the morning and evening, every day for 12 weeks.
DRUG4% Hydroquinone Topical Cream4% Hydroquinone Topical Cream applied to the affected areas twice a day, in the morning and evening, every day for 12 weeks.
OTHERSkinMedica Facial CleanserSkinMedica facial cleanser applied to the face as directed.
OTHERSkinMedica Rejuvenative MoisturizerSkinMedica rejuvenative moisturizer applied to the face as directed.
OTHERSkinMedica Essential Defense Mineral Shield Broad Spectrum SPF 35 SunscreenSkinMedica Essential Defense Mineral Shield Broad Spectrum SPF 35 sunscreen applied to the face as directed.

Timeline

Start date
2016-12-13
Primary completion
2017-10-09
Completion
2017-10-09
First posted
2016-11-30
Last updated
2018-12-19
Results posted
2018-11-07

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT02977507. Inclusion in this directory is not an endorsement.