DRKS00026646尚未招募不适用
Identification of Biological and Psychosocial Factors of Symptom Persistence in Pruritus - SOMACROSS-Pruritus-4
Kompetenzzentrum Chronischer Pruritus, Klinik für Hautkrankheiten, Universitätsklinikum Münster0 个研究点目标入组 200 人开始时间: 2021年9月17日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Age = 18 years
- •Group 1: Acute atopic dermatits (aAD)
- •acute eczema = 4 weeks at baseline
- •previous eczema free interval for at least 6 months
- •pruritus intensity (NRS worst pruritus of the last 24h): =5/10
- •Group 2: chronic atopic dermatitis (cAD)
- •clinical diagnosis of atopic dermatitis, for at least 6 months
- •chronic pruritus (= 6 weeks duration)
- •pruritus intensity (NRS worst pruritus of the last 24h): =5/10
- •Group 3: chronic pruritus on non-lesional skin (CPNL)
- •pruritus on non-lesional skin (absence of a dermatosis or scratch lesions)
- •chronic pruritus (= 6 weeks duration)
- •pruritus intensity (NRS worst pruritus of the last 24h): =5/10
- •Group 4: healthy controls
- •non-lesional skin (absence of a dermatosis or scratch lesions)
- •no pruritus (pruritus intensity NRS worst pruritus of the last 24h: 0/10)
- •no history of atopic dermatitis, allergic asthma, type 1 allergies
- •no chronic pain syndrome or intake of analgesic drugs
排除标准
- •- Acute exacerbation of a dermatosis (exception: atopic dermatitis) or cutaneous infection
- •- pregnancy, breastfeeding
- •- drug or alcohol abuse
- •- allergy against local anesthetics
- •- Tendency of developing keloids
- •- Chronic pain, fibromyalgia
- •- Intake of antihistamines, systemic steroids, systemic immunosuppressants, gabapentinoids or analgesics in the previous 4 weeks (intake of antidepressants is allowed if not as antipruritic medication).
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