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
| Type | Name | Description |
|---|---|---|
| OTHER | Lytera 2.0 | Lytera 2.0 applied to the affected areas twice a day, in the morning and evening, every day for 12 weeks. |
| DRUG | 4% Hydroquinone Topical Cream | 4% Hydroquinone Topical Cream applied to the affected areas twice a day, in the morning and evening, every day for 12 weeks. |
| OTHER | SkinMedica Facial Cleanser | SkinMedica facial cleanser applied to the face as directed. |
| OTHER | SkinMedica Rejuvenative Moisturizer | SkinMedica rejuvenative moisturizer applied to the face as directed. |
| OTHER | SkinMedica Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen | SkinMedica 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT02977507. Inclusion in this directory is not an endorsement.