跳至主要内容
临床试验/DRKS00022298
DRKS00022298招募中不适用

Pruritus and Psoriasis - experimental analyses of itch in patients with psoriasis - PruriPsoExp

Klinik für Dermatologie, UKSH Campus Kiel0 个研究点目标入组 60 人开始时间: 2020年10月28日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60

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

  • Patients with psoriasis for at least 3 months with and without pruritus. Controlgroup (no skin diseases, no itch).
  • - Patients with pruritus should suffer from pruritus for at least 6 weeks
  • - patients with a stable anti-psoriatic treatment for at least 4 weeks (with the exemption of UV-therapy and systemic corticosteroids) and/or therapy-naiv patients.
  • - no topical therapy for at least 3 weeks prior to testing in the location that will be evaluated
  • - One psoriatic lesion should be located on the back and/or thighs and/or buttocks.

排除标准

  • - pregnancy or breastfeeding
  • - systemic corticosteroids or uv-therapy within four weeks prior to testing
  • - intake of NSAR, analgetics, opioids or other medikations with an influence on itch within 7 days prior to testing.
  • - intake of antidepressents or medication against migraine within four weeks prior to testing
  • - intake of gabapentin within four weeks prior to testing
  • - application of emolients on the day of testing
  • - known intolerance of capsaicin, histamin, cowhadge or other relevant substances
  • - other skin lesions than psoriasis (e.g. infection, tattoos) in the testlocation
  • - patients with a known history of atopy
  • - patients with a known history of polyneurophaty or other neurological diseases
  • - patients with a history of diabetes
  • - patients with a history of backpain
  • - diseases that in the discretion of the investigators do not allow testing (e.g. psychosomatic or psychological diseases).
  • - skin type IV-VI (Fitzpatrik)
  • - patients/controlgroup unable to consent
  • - drug or alcohol abuse

研究者

发起方
Klinik für Dermatologie, UKSH Campus Kiel

相似试验