Condition category
Skin and Connective Tissue Diseases
Date applied
01/05/2018
Date assigned
12/06/2018
Last edited
01/06/2018
Prospective/Retrospective
Retrospectively registered
Overall trial status
Completed
Recruitment status
No longer recruiting

Plain English Summary

Background and study aims
Melasma is a common pigmentary disorder characterized by hyperpigmented and dark patched skin. Melasma occurs in all populations worldwide and mainly affects adult women with darker skin in their reproductive age living in areas with intense sun exposure. Some people like to try to reduce the look of the patches using treatments to reduce the lesions. This study aims to examine if a new treatment option, using a topical formulation with a new inhibitor of human tryosinase, can reduce the look of the patches and spots.

Who can participate?
Women aged 18 to 65 years old who have Fitzpatrick skin type II-IV and who have mild to moderate hyperpigmentation due to melasma on both sides of the face

What does the study involve?
Participants have one side of their face treated with a formulation containing a new active ingredient to reduce hyperpigmentation and are randomly allocated to either leave the other side of the face untreated or treat the other side of the face with a 2% hydroquinone-containing formulation. Hyperpigmentation is assessed at 4, 8 and 12 weeks after treatment to determine if there is any impact of the two different treatments.

What are the possible benefits and risks of participating?
The active ingredient may reduce the visibility of the hyperpigmented patches. If participants are sensitive individuals, irritation might occur in the treated skin sites.

Where is the study run from?
Thomas J. Stephens & Associates, Inc., Texas Research Center (USA)

When is the study starting and how long is it expected to run for?
September 2015 to September 2016

Who is funding the study?
Beiersdorf AG (Germany)

Who is the main contact?
Dr Ludger Kolbe

Trial website

Contact information

Type

Scientific

Primary contact

Dr Ludger Kolbe

ORCID ID

http://orcid.org/0000-0001-8608-8901

Contact details

Beiersdorf AG
BF 519
Unnastrasse 48
Hamburg
20245
Germany

Additional identifiers

EudraCT number

ClinicalTrials.gov number

Protocol/serial number

C15-D216 (49595)

Study information

Scientific title

A clinical trial to assess and compare the efficacy and tolerance of two different product formulas used by
women with mild to moderate melasma

Acronym

Study hypothesis

The tyrosinase Inhibitor W630 reduces hyperpigmentation on human skin.

Ethics approval

IntegReview Institutional Review Board (IRB) located in Austin, Texas, 12/11/2015, ref: IORG0000689

Study design

Single-center double-blinded randomized split-face controlled study

Primary study design

Interventional

Secondary study design

Randomised controlled trial

Trial setting

Other

Trial type

Treatment

Patient information sheet

Not available in web format, please use the contact details to request the patient information sheet.

Condition

Mild to moderate hyperpigmentation due to melasma on both sides of the face, but otherwise healthy skin

Intervention

Prospective subjects are invited to an eligibility screening and advised to avoid application of topical moisturizing products on the face for at least 3 days prior to the screening. At the baseline visit, subjects are clinically graded for overall hyperpigmentation (mottled and discrete), discrete hyperpigmentation, overall appearance, radiance, skin roughness (visual) separately on the right and left sides of the face. Subjects are further assessed for melasma area and severity (MASI) parameters separately on the global right and left sides of the face. A total of two full-face images are taken of each subject (right side and left side views) under standard lighting 1 and 2, and cross-polarized lighting.

Subjects are randomly assigned to cell A or cell B according to a predetermined randomization scheme. Subjects in both cells are distributed a product containing the active ingredient, and subjects in cell B are additionally given an on the market 2% hydroquinone-containing formulation. For a 12-week treatment period, the participants treat one side of the face with the active ingredient formulation twice a day and leave the other side of the face either untreated or treat it twice daily with the 2% hydroquinone-containing formulation.

Evaluation of skin hyperpigmentation before treatment (baseline) and after 4, 8, and 12 weeks of treatment. Comparison (overall and discrete hyperpigmentation, HEMI MASI) to baseline and 2% hydroquinone-treated site.

Intervention type

Other

Phase

Drug names

Primary outcome measure

Clinical grading of overall hyperpigmentation (mottled and discrete) and discrete hyperpigmentation (MASI assessment) at baseline, week 4, week 8, and week 12

Secondary outcome measures

Tolerability assessed using a self-assessment questionnaire at baseline, week 4, week 8, and week 12

Overall trial start date

11/09/2015

Overall trial end date

29/09/2016

Reason abandoned (if study stopped)

Eligibility

Participant inclusion criteria

1. Women 18 to 65 years of age having general good health
2. Fitzpatrick skin type II-IV
3. Individuals with mild to moderate hyperpigmentation due to melasma on both sides of the face (score of 3-6 on according to the modified Griffiths’ scale1, where 0 = none and 9 = severe, halfpoints are acceptable to qualify)
4. Ability to understand the study concept (intellectual capacity and language skills) and to comply with the test schedule and study rules
5. Participant is willing and able to give written informed consent

Participant type

Healthy volunteer

Age group

Adult

Gender

Female

Target number of participants

60 subjects, 30 per cell

Participant exclusion criteria

1. Individuals who had laser resurfacing procedure, deep skin peel, Botox or injection with a dermal filler, or cosmetic procedures on the face within 6 months prior to enrollment
2. Individuals who had used depigmenting products within 2 months prior to enrollment
3. Individuals who have used any topical medications on the face for hyper pigmented lesions or other conditions, or use of photosensitizing medication or procedures (including corticosteroids, hydroquinone, alpha-hydroxy, beta-hydroxy or kojic acid, retinoic acid, retinol, salicylic acid, Vitamin C and Vitamin D preparations or derivatives thereof), bleaching products on the face, UV light therapy, topical prescription treatments, topical tretinoin on the face less than 30 days prior to the study entry
4. Individuals who have used Acitretin, isotretinoin, systemic retinoids (e.g. Accutane), methotrexate, or photoallergic, phototoxic or photo-sensitizing drugs within 6 months of baseline (and will refrain from use during the study)
5. Individuals who have had prior facial microdermabrasion (light or medium skin peel) treatment within 6 weeks prior to study entry.
6. Individuals diagnosed with known allergies to facial skin care products
7. Individuals who are nursing, pregnant, or planning to become pregnant during the study according to subject self-report including those who are not using an acceptable method of contraception throughout the study
8. Individuals with a history of skin cancer
9. Individuals having a health condition and/or pre-existing or dormant dermatologic disease on the face (e.g., psoriasis, rosacea, acne, eczema, seborrheic dermatitis, severe excoriations etc.) that the Investigator or designee deems inappropriate for participation or could interfere with the outcome of the study
10. Individuals with a history of immunosuppression/immune deficiency disorders (including (HIV infection or AIDS) or currently using immunosuppressive medications (e.g., zathioprine, belimumab, cyclophosphamide, Enbrel, Imuran, Humira, mycophenolate mofetil, methotrexate, prednisone, Remicade, Stelara.) and/or radiation as determined by study documentation
11. 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

Recruitment start date

20/11/2015

Recruitment end date

08/07/2016

Locations

Countries of recruitment

United States of America

Trial participating centre

Thomas J. Stephens & Associates, Inc. Texas Research Center
1801 North Glenville Drive, Suite 200
Richardson
75081
United States of America

Sponsor information

Organisation

Beiersdorf AG

Sponsor details

Unnastrasse 48
Hamburg
20245
Germany

Sponsor type

Industry

Website

Funders

Funder type

Industry

Funder name

Beiersdorf AG

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Results and Publications

Publication and dissemination plan

To be published after completion of all tests. Study protocol and statistical analysis plan will be part of the planned publication.

IPD sharing statement:
The datasets generated and/or analyzed during this study will be included in the subsequent results publication.

Intention to publish date

01/10/2018

Participant level data

Other

Basic results (scientific)

Publication list

Publication citations

Additional files

Editorial Notes