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临床试验/NCT04377828
NCT04377828Unknown不适用

Evaluation of the Improvement of Pigmented Skin Lesions in Patients With Mastocytosis After Performing 2 Sessions of Pigment Laser : Pilot Study Conducted at a Reference Centre Mastocytoses (LaserMasto)

University Hospital, Toulouse2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2020年9月14日最近更新:
适应症

试验速览

阶段
不适用
入组人数
34
试验地点
2
主要终点
Global clinical evolution of the skin M4 - Blind evaluator

研究概览

简要总结

Cutaneous mastocytosis can be isolated or associated with systemic involvement. Urticaria pigmentosa affects around 80 to 85% of adult patients with cutaneous mastocytosis. It is also frequently present in patients with mastocytosis associated with systemic involvement (80% of patients in our experience).

This skin damage is one of the causes of deterioration in quality of life in patients with mastocytosis, through the loss of self-esteem, due to the appearance of lesions. However there are not treatment for urticaria pigmentosa.

Skin involvement in mastocytosis is linked to the accumulation of abnormal mast cells in the dermis. However, the mast cells are not pigmented and the brown-brown color characteristic of Urticaria pigmentosa is explained by melanin pigmentation of the epidermal basal layer.

详细描述

Cutaneous mastocytosis can be isolated or associated with systemic involvement. Urticaria pigmentosa affects around 80 to 85% of adult patients with cutaneous mastocytosis. It is also very frequently present in patients with mastocytosis associated with systemic involvement (80% of patients in our experience).

This skin damage is one of the causes of deterioration in quality of life in patients with mastocytosis, through the loss of self-esteem, due to the appearance of lesions. However ,there is not a treatment for urticaria pigmentosa.

Skin involvement in mastocytosis is linked to the accumulation of abnormal mast cells in the dermis. However, the mast cells are not pigmented and the brown-brown color characteristic of pigmentary urticaria is explained by melanin pigmentation of the epidermal basal layer. This characteristic is often described on skin biopsies of pigmentary urticaria analyzed in hematoxilin-eosin.

The 532 nm Q-Switched laser is known to improve lesions characterized by the presence of melanin pigment in the basal layer of the epidermis, with very little risks. This later is explained by the reduced penetration of light at 532 nm into the skin and the emission time of the laser light which is very low (of the order of a few nanoseconds) for Q-Switched lasers. In the literature, 2 case reports report an efficiency of the laser at 532 nm in this indication in adults.

The hypothesis of this study is that 2 sessions of Q-switched laser could improve the skin lesions of urticaria pigmentosa, leading to an improvement in self-esteem.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with mastocytosis (diagnosis confirmed clinically according to international criteria)
  • Patient with pigmented skin lesions, of moderate to very severe severity (by comparison with a 4-point photographic scale: light, moderate, severe and very severe)
  • Major patient aged ≥ 18 years.
  • Patient with social security coverage
  • Patient having given written, free and informed consent to participate in the study

排除标准

  • Patients with mastocytosis, without skin lesions
  • Patient with pigmented skin lesions, only of mild severity (by comparison with a 4-point photographic scale: mild, moderate, severe and very severe)
  • Patient with another cutaneous mastocytosis phenotype
  • Patient treated by a treatment known as a cytoreductive for mastocytosis: alpha interferon, cladribine, imatinib, midostaurin or any cytoreductive treatment being evaluated by clinical trial in mastocytosis
  • Patient under guardianship, or under curatorship, or not fluent in the French language or unable to understand and complete the study questionnaires
  • pregnant or breastfeeding women
  • Patients with tanned skin following photoexposure within 3 weeks of starting the study

结局指标

主要结局

Global clinical evolution of the skin M4 - Blind evaluator

时间窗: Month 4

Global clinical evolution with IGA " Improvement Global Assessment" (scale with 5 points : no improvement or aggravation/minimal improvement/moderate improvement/significant improvement/complete disappearance) by blind evaluator in month 4 versus baseline

次要结局

  • Psychological impact - Month 9(Month 9)
  • Global clinical evolution of the skin M1 - Blind evaluator(Month 1)
  • Global clinical evolution of the skin M4 - Principal investigator(Month 4)
  • Severity of a targeted pigment skin lesion - M4(Month 4)
  • Severity of a targeted pigment skin lesion - M9(Month 9)
  • Psychological impact - baseline(Baseline)
  • Global clinical evolution of the skin M9 - Blind evaluator(Month 9)
  • Global clinical evolution of the skin M1 - Principal investigator(Month 1)
  • Severity of a targeted pigment skin lesion - M1(Month 1)
  • Global clinical evolution of the skin M9 - Principal investigator(Month 9)
  • Psychological impact - Month 4(Month 4)
  • Patient satisfaction - Month 1(month 1)
  • global patient satisfaction(month 9)
  • Pigment laser tolerance(Day 1)
  • Patient satisfaction - Month 4(month 4)
  • Patient satisfaction - Month 9(month 9)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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