N/A
N=18
Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topical Products in Participants With Moderate Facial Melasma
Melasma
Bottom Line
View on ClinicalTrials.gov: NCT02977507 ↗Enrolled (actual)
18
Serious AEs
5.6%
Results posted
Nov 2018
Primary outcome: Primary: Change From Baseline in Melasma Severity Rating Scale Score to Week 12 — 2.1; 2.1; -0.3; -0.8 score on a scale — p=0.041
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lytera 2.0 (Other); 4% Hydroquinone Topical Cream (Drug); SkinMedica Facial Cleanser (Other); SkinMedica Rejuvenative Moisturizer (Other); SkinMedica Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Allergan
- Primary completion
- Oct 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline in Melasma Severity Rating Scale Score to Week 12 |
2.1; 2.1; -0.3; -0.8 | 0.041 sig |
| PRIMARY Change From Baseline in Overall Hyperpigmentation Scale Score to Week 12 |
4.8; 4.8; -0.8; -1.7 | 0.002 sig |
| PRIMARY Change From Baseline in Melasma Area and Severity Index (MASI) Score to Week 12 |
9.0; 8.9; -1.2; -3.1 | 0.004 sig |
| SECONDARY Number of Participants by Responses for Self-Assessment Questionnaire: Overall Improvement in Skin Condition |
5; 2; 8; 11; 3; 3 | — |
| SECONDARY Number of Participants by Responses for Self-Assessment Questionnaire: Overall Satisfaction With the Test Product |
3; 6; 9; 9; 5; 3 | — |
| SECONDARY Number of Participants by Responses for Self-Assessment Questionnaire: Test Product Preference |
6; 12; 3; 13; 3; 13 | — |
| SECONDARY Change From Baseline in Melasma Quality of Life (MELASQOL) Scale Total Score to Week 12 |
45.9; 46.2; -15.0; -21.7 | 0.003 sig |
| SECONDARY Investigator's Global Improvement Assessment for Overall Hyperpigmentation Score to Week 12 |
1.1; 1.8 | — |
| SECONDARY Change From Baseline in Mexameter Measurement of Target Hyperpigmentation Lesion to Week 12 |
581.1; 587.1; 544.5; -3.0; -26.5; -2.4 | 0.569 |
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.
Eligibility Criteria
Inclusion Criteria
- Female or male aged 18+ years with general good health
- Individuals with dark patches on both sides of their face
- Individuals that are willing to provide written informed consent and are able to read, speak, write, and understand English.
- Individuals willing to sign have their photographs taken during the study and are willing to sign a photography release.
- Willing to stop all facial treatments during the course of the study including botulinum toxin, injectable fillers, microdermabrasion, Intense pulsed light (IPL), peels, facials, waxing, laser treatments and tightening treatments. Threading is allowed but not facial laser hair removal.
- Willingness to cooperate follow all study requirements for the duration of the study and to report any changes in health status or medications, adverse event symptoms, or reactions immediately.
- Willingness to not begin using any new cosmetic facial make-up during the study. If you regularly use cosmetic facial make-up, you must have used the product(s) without any issues for at least 2 weeks prior to starting the study.
- Willingness to avoid sun exposure to the face as much as possible, (including tanning beds), especially from 10 AM to 2 PM. Protective clothing (i.e. hats) and the provided sunscreen should be worn prior to and during any exposure.
Exclusion Criteria
- Individuals diagnosed with known allergies to study provided skin care products.
- Individuals who are nursing, pregnant, or planning to become pregnant during the study according to subject self-report.
- Individuals with a history of skin cancer.
- Individuals having a health condition on the face (e.g., psoriasis, rosacea, acne, eczema, seborrheic dermatitis, severe excoriations etc.).
- Individuals with a history of immunosuppression/immune deficiency disorders (including (Human immunodeficiency virus (HIV) infection or Acquired Immune Deficiency Syndrome (AIDS)) or currently using immunosuppressive medications (e.g., azathioprine, belimumab, cyclophosphamide, Enbrel, Imuran, Humira, mycophenolate mofetil, methotrexate, prednisone, Remicade, Stelara.) and/or radiation.
- Individuals with an uncontrolled disease such as asthma, diabetes, hypertension, hyperthyroidism, or hypothyroidism. Individuals having multiple health conditions may be excluded from participation even if the conditions are controlled by diet, medication, etc.
- Individuals with any planned surgeries and/or invasive medical procedures during the course of the study.
- Individuals who are currently participating in any other facial usage study or have participated in any clinical trial within 4 weeks prior to inclusion into the study.
- Individuals who have observable suntan, scars, nevi, excessive hair, etc. or other dermal conditions on the face that might influence the test results in the opinion of the Investigator or designee.
- Individuals who started hormone replacement therapies (HRT) or hormones for birth control less than 3 months prior to study entry or who plan on starting, stopping, or changing doses of HRT or hormones for birth control during the study.
- Individuals who used any of the following medications or had any of the listed procedures within the listed time frame prior to the study start date:
- Retin-A®, Retin-A Micro®, Renova®, Avita®, Tazorac®, or Differin® within 3 months
- Had a light-depth chemical peel or microdermabrasion within 1 month
- Had a medium-depth chemical peel, medium-depth microdermabrasion, any systemic steroids, non-ablative laser, light and/or radio frequency or fractional laser resurfacing of the face and neck within 3 months
- Any systemic retinoid (e.g. Soriatane®, Accutane®, Roche Dermatologics) within 12 months
- Any topical or systemic antibiotics, such as minocycline, or any other known medications that can cause photosensitivity, such as hydrochlorothiazide, lasix, amiodarone, within 1 month
- Any topical tretinoin product or derivative, imiquimod, 5-fluorouracil, o
Data sourced from ClinicalTrials.gov (NCT02977507). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.