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临床试验/NCT06516224
NCT06516224尚未招募不适用

Evaluation of the Efficacy of the Anti-pigmenting Effect of a Routine of Facial Products in Subjects With Melasma

Cosmetique Active International1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2024年7月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
150
试验地点
1
主要终点
antipigmenting assessment

研究概览

简要总结

This 6 month, comparative study assesses the benefit of a dermocosmetic regimen (Serum B3 + B3 retinol night cream) for 6 months compared to hydroquinone 4% (the gold standard in hyperpigmentation) followed by the dermocosmetic regimen for 3 months or the Kligman Trio for 3 months followed by the dermocosmetic regimen for 3 months in adult women with melasma on the face.

详细描述

Study objective

  1. Assessing the antipigmenting efficacy of the routine (serum B3 + B3 retinol night cream) in women with melasma.
  2. Evaluation of Kligman Trio (KT) (Vitacid Plus) compared to the routine (serum B3 + B3 retinol night cream)
  3. Evaluation of Hydroquinone 4% (HQ 4%) compared to the routine (serum B3 + B3 retinol night cream).
  4. Assessment of the routine maintenance with SERUM B3 + retinol B3 night cream after 3 months of use of Klingman Trio (KT)(Vitacid plus) and HQ4%

Primary endpoint:

o Improvement of mMASI and MASI

Secondary endpoints:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

Subjects will be randomized in three groups and will be treated differently taking into account only the original Melasma Area Severity Index (MASI) score at baseline:

• An adaptive randomization scheme (minimization method) will be used to determine the treatment group (among the 3 available) to which eligible subjects will be enrolled in. This strategy will ensure a balance between treatment groups for one important prognostic factor, identified as 'baseline MASI'. When a new subject is eligible for randomization, the algorithm verifies the average MASI of the subjects in each group. The new subject will be allocated to a group in such a way that the imbalance is minimized among the groups.

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •18-65 years
  • •Phototype II-V
  • •50% with sensitive skin (declarative);
  • •Subjects should be affected by well defined symmetrical (on both sides of the face) epidermal melasma (clinically diagnosed under Wood's light examination) lasting since more than a year

排除标准

  • •Subjects under topical or systemic retinoids;
  • •Subjects having used topical tretinoin within 3 months or topical hydroquinone within 6 months prior to inclusion;
  • •Subjects under systemic immunosuppressants and considered immune compromised
  • •Subjects under active treatment of melasma (including topicals or procedures) within the last 3 months
  • •Pregnant women and/or breastfeeding women
  • •Subjects with a recent change in contraception (since less than 6 months);
  • •Subjects known allergy to any component of tested product;
  • •Subjects not presenting with the conditions needed to comply with the protocol;
  • •Subjects without any other dermatological conditions on the face
  • •Subject under menopause phase with hormonal replace therapy
  • •Subjects in the initial phase, change or discontinuation of hormonal treatment (estroprogesterone, cyproteron acetate, androgenic...) in the last 3 months;
  • •Subjects currently using any medication, which in the opinion of the investigator, may affect the evaluation of the study product, or place the subject at undue risk.
  • •Subjects unable to give their informed consent.

研究组 & 干预措施

Group 1

Experimental

dermocosmetic regimen consisting in Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream (all Vichy Laboratoires, France) for 6 months + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+

干预措施: Liftactiv® B3 Serum (Other)

Group 1

Experimental

dermocosmetic regimen consisting in Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream (all Vichy Laboratoires, France) for 6 months + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+

干预措施: Liftactiv® B3 retinol night cream (Other)

Group 1

Experimental

dermocosmetic regimen consisting in Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream (all Vichy Laboratoires, France) for 6 months + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+

干预措施: Sunscreen UVAage® Inter SPF 50+ (Other)

Group 1

Experimental

dermocosmetic regimen consisting in Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream (all Vichy Laboratoires, France) for 6 months + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+

干预措施: Mineral 89 cream (Other)

Group 2

Active Comparator

hydroquinone 4% (HQ4%, Hydroquinona 40 mg/g, Germed, Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Liftactiv® B3 Serum (Other)

Group 2

Active Comparator

hydroquinone 4% (HQ4%, Hydroquinona 40 mg/g, Germed, Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Liftactiv® B3 retinol night cream (Other)

Group 2

Active Comparator

hydroquinone 4% (HQ4%, Hydroquinona 40 mg/g, Germed, Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Sunscreen UVAage® Inter SPF 50+ (Other)

Group 2

Active Comparator

hydroquinone 4% (HQ4%, Hydroquinona 40 mg/g, Germed, Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Mineral 89 cream (Other)

Group 3

Active Comparator

Combination of hydroquinone, resorcinol corticosteroid (Kligman Trio, Vitacid Plus Cream, Claredor Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Liftactiv® B3 Serum (Other)

Group 3

Active Comparator

Combination of hydroquinone, resorcinol corticosteroid (Kligman Trio, Vitacid Plus Cream, Claredor Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Liftactiv® B3 retinol night cream (Other)

Group 3

Active Comparator

Combination of hydroquinone, resorcinol corticosteroid (Kligman Trio, Vitacid Plus Cream, Claredor Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Sunscreen UVAage® Inter SPF 50+ (Other)

Group 3

Active Comparator

Combination of hydroquinone, resorcinol corticosteroid (Kligman Trio, Vitacid Plus Cream, Claredor Brazil) for 3 months followed by the dermocosmetic regimen (Liftactiv(® B3 serum + Liftactiv® B3 retinol night cream + Mineral 89 cream + Sunscreen UVAage Inter SPF 50+) for 3 months

干预措施: Mineral 89 cream (Other)

结局指标

主要结局

antipigmenting assessment

时间窗: Day 168

Melasma Area Severity Index(MASI)

antipigmenting assessment

时间窗: Day 84

Melasma Area Severity Index (MASI)

次要结局

  • Subject global efficay rating(Day 168)
  • confocal(Day 168)
  • Investigator global efficay rating(Day 168)
  • transepidermal water loss(Day 168)
  • skin hydration(Day 168)
  • exposome questionnaire(baseline)
  • Cosmetic acceptability(Day 168)
  • Evolution of quality of life(Day 156)
  • antipigmenting assessment(Day 140)
  • Clinical assessment (fine lines, skin tone, radiance, texture and elasticity)(Day 168)
  • Clinical scoring target lesion comparing to surrounding skin(Day 168)
  • Clinical scoring hyperpigmentation(Day 168)
  • Investigator Global Assessment (IGA) assessment(Day 168)
  • images(Day 168)
  • Skin quality(Day 168)
  • Melasma status(baseline)
  • adverse events(Day 168)
  • Evolution of quality of life(Day 140)
  • images(baseline)
  • Investigator global efficay rating(Day 140)
  • Cosmetic acceptability(Day 28)
  • Cosmetic acceptability(Day 56)
  • Cosmetic acceptability(Day 84)
  • Cosmetic acceptability(Day 112)
  • Cosmetic acceptability(Day 140)
  • adverse events(Day 28)
  • Evolution of quality of life(Day -28)
  • adverse events(Day 56)
  • Evolution of quality of life(baseline)
  • Evolution of quality of life(Day 28)
  • adverse events(Day 84)
  • Evolution of quality of life(Day 84)
  • Evolution of quality of life(Day 56)
  • Clinical scoring hyperpigmentation(Day 28)
  • Clinical scoring hyperpigmentation(Day 56)
  • Clinical scoring hyperpigmentation(Day 84)
  • Clinical scoring hyperpigmentation(Day 112)
  • Evolution of quality of life(Day 112)
  • antipigmenting assessment(Day 112)
  • antipigmenting assessment(Day 56)
  • antipigmenting assessment(Day-28)
  • antipigmenting assessment(baseline)
  • antipigmenting assessment(Day 28)
  • Investigator Global Assessment (IGA) assessment(Day -28)
  • Investigator Global Assessment (IGA) assessment(baseline)
  • Investigator Global Assessment (IGA) assessment(Day 28)
  • Investigator Global Assessment (IGA) assessment(Day 56)
  • Investigator Global Assessment (IGA) assessment(Day 84)
  • Investigator Global Assessment (IGA) assessment(Day 112)
  • Investigator Global Assessment (IGA) assessment(Day 140)
  • Clinical assessment (fine lines, skin tone, radiance, texture and elasticity)(Day -28)
  • Clinical assessment (fine lines, skin tone, radiance, texture and elasticity)(baseline)
  • Clinical assessment (fine lines, skin tone, radiance, texture and elasticity)(Day 28)
  • Clinical assessment (fine lines, skin tone, radiance, texture and elasticity)(Day 84)
  • Clinical scoring hyperpigmentation(baseline)
  • Clinical scoring hyperpigmentation(Day 140)
  • Clinical scoring target lesion comparing to surrounding skin(baseline)
  • Clinical scoring target lesion comparing to surrounding skin(Day 28)
  • Clinical scoring target lesion comparing to surrounding skin(Day 56)
  • Clinical scoring target lesion comparing to surrounding skin(Day 84)
  • Clinical scoring target lesion comparing to surrounding skin(Day 112)
  • Clinical scoring target lesion comparing to surrounding skin(Day 140)
  • Subject global efficay rating(Day 28)
  • Subject global efficay rating(Day 56)
  • Subject global efficay rating(Day 84)
  • Subject global efficay rating(Day 112)
  • Subject global efficay rating(Day 140)
  • Investigator global efficay rating(Day 28)
  • Investigator global efficay rating(Day 56)
  • Investigator global efficay rating(Day 84)
  • Investigator global efficay rating(Day 112)
  • images(Day 28)
  • images(Day 56)
  • images(Day 84)
  • images(Day 112)
  • images(Day 140)
  • Skin quality(baseline)
  • Skin quality(Day 28)
  • Skin quality(Day 56)
  • Skin quality(Day 84)
  • Skin quality(Day 112)
  • Skin quality(Day 140)
  • transepidermal water loss(baseline)
  • transepidermal water loss(Day 28)
  • transepidermal water loss(Day 56)
  • transepidermal water loss(Day 84)
  • transepidermal water loss(Day 112)
  • transepidermal water loss(Day 140)
  • skin hydration(baseline)
  • skin hydration(Day 28)
  • skin hydration(Day 56)
  • skin hydration(Day 84)
  • skin hydration(Day 112)
  • skin hydration(Day 140)
  • confocal(baseline)
  • confocal(Day 84)
  • adverse events(baseline)
  • adverse events(Day 112)
  • adverse events(Day 140)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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