Efficacy and Tolerance of D-pigment Versus Moisturizer in Hands' Lentigo Lesions With or Without Laser Therapy

Pierre Fabre Dermo Cosmetique40 enrolled

Overview

Pierre Fabre Dermo-Cosmétique has commercialized a cosmetic product (D-pigment rich texture) for treatment of hyperpigmentation. The aim of this study is to evaluate the efficacy of D-pigment after laser therapy, through its action on peri-lesional areas, in obtaining better cosmetic effect.

Many studies have shown the efficacy of topical products such as hydroquinone, tretinoin, ascorbic and phytic acid... The combination of topical agents has shown better improvement of lentigos aspect. Many physical therapy such as chemical peels, cryosurgery, dermabrasion, and pigment-specific lasers show good results. The combination of physical and topical therapies may be beneficial to patients. For example, the use of combination topical therapy may be used after cryotherapy as a maintenance therapy to diminish the risk of relapse. Laser therapy is very efficient on visible lesion, but not to prevent lesions apparition. A cosmetic topical depigmenting product may be a support of laser therapy, to prevent lentigos apparition in peri-lesional areas. Furthermore, Post-inflammatory hyperpigmentation (PIH) is a common adverse effect seen with laser, occurring in approximately 35-40% of patients with Fitzpatrick skin types I-III. Another study related that 28% of study population has post-inflammatory hyperpigmentation. A cosmetic topical depigmenting product may be a support of laser therapy, to prevent possible laser side effect. Pierre Fabre Dermo-Cosmétique has commercialized a cosmetic product (D-pigment rich texture) for treatment of hyperpigmentation. The aim of this study is to evaluate the efficacy of D-pigment as a support of a laser therapy, through its action on peri-lesional areas. The expected effect is to show the efficacy of D-pigment in post laser long-term treatment, having a more homogenous skin colour on the D-pigment hand versus the moisturizer hand. The subjects will benefit from a strengthened follow-up by the investigator (one visit every 3 months). After the completion of the study, a complete hands laser treatment will be done for each subject and D-pigment tubes will be offered to the subjects for a 6 months application period.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Lentigo Hyperpigmentation

Interventions

D-Pigment rich textureOTHER

Hydrance optimale richeOTHER

Eligibility

Sex: ALLMin age: 50 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Subject consenting on the use of photos for scientific and commercial purposes, * Subject having signed his/her written informed consent. * Subject treated by laser therapy in the previous 15 to 30 days * Subject having 5 to 10 lentigos on the surface of each hands * Subject having lentigos graded 6 or more on the severity grading scale * Subject with same lentigo severity in each hand. Exclusion Criteria: * Subject who has planned to stay for more than 15 days in an area with an important increase in sun exposure conditions compared to his/her usual place of residence, * Subject who has planned to sun expose himself/herself more than 7 days, * Women with childbearing potential * Participation to an other clinical trial in the previous month or during the study, * Subject who is not able to understand the information (for linguistic or psychiatric reasons), to give informed consent, * Subject who, in the judgement of the investigator, is not likely to be compliant with study-related constraints during the study (daily product application during one year), * Subject who has forfeited her freedom by administrative or legal decision, or who is under guardianship. Criteria related to pathologies: * Hyperpigmentation other than lentigos or other hypermelanosis (post-inflammatory laser or chemical melanosis) on the hands, * Diabetic subject, * Chronic or progressive disease which may interfere with the study in the opinion of the investigator, * Pathology, skin disorder or lesions other than lentigo (psoriasis, atopic dermatitis, mycose, intertrigo, sunburn…) at the dorsum of the hand which could interfere with the evaluation, * Systemic infectious pathology, * Hypersensitivity, allergy or intolerance to retinaldehyde or any component of the formulation. Criteria related to treatments: * Treatment by depigmenting cosmetic products on the hands within 4 weeks prior to inclusion, * Treatment by depigmenting treatment containing hydroquinone or any depigmenting drug on the hands (e.g. topical retinoids, topical steroids, …) within 8 weeks prior to inclusion, * Previous treatment by chemical peels, dermabrasions on the hands within one year prior to inclusion, * Treatment by photosensitive agents within 8 weeks prior to inclusion.

Outcomes

Primary Outcomes

Change from baseline skin color homogeneity at 12 months by blinded evaluation from standardized photos.

Scoring homogeneity will be assessed through 2 Visual Analogue Scales. One VAS grades the surface affected by lentigo on observed area, no lentigo corresponding to 0 and area completely hidden by lentigo to 10. The second VAS grades differences between lighter and darker skin of areas, same color skin corresponding to 0 and extremely dark lentigo to 10. Sum of the two VAS (0 to 20) represents the homogeneity of the skin color Blinded evaluation. During all the visits, an investigator will take photos. After visits, photos will be renamed and resampled. The investigator who will evaluate the parameter may be independent from that one who took photos. Each parameter will be evaluated by the same person avoiding thus quotation bias. They will be evaluated on each area blinded from product applied and from time evaluated. The appraiser will quote at the same time the pictures obtained for one subject, for one hand, at Baseline and at 12 months.

Time frame: Assessed at 12 months versus baseline.

Secondary Outcomes

Change over time of skin color homogeneity by blinded evaluation from standardized photos.

Time frame: assessed at Day 0, 3 months, 6 months, and 9 months.

Data from ClinicalTrials.gov

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