跳至主要内容
临床试验/NCT06414382
NCT06414382尚未招募不适用

Pilot Study on Koebner Induction in Patients With Plaque Psoriasis

Skane University Hospital0 个研究点目标入组 15 人开始时间: 2024年5月7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
15
主要终点
Positive Koebner Phenomena (K+)

研究概览

简要总结

Patients (n=15) with skin psoriasis, minimum age 18 years, without systemic immunomodulatory treatment will be subject to Koebner induction on arms and legs given that they have given written consent and that they have self-reported Koebner.

详细描述

PSODEEP2 PILOT STUDY

Study subject recruitation:

Individuals fulfilling inclusion and exclusion criteria will be identified and contacted from the PSODEEP1 study (ethical application2023-00571-02 and 2022-02835-01), advert in social media, advert in newsletter/magazine sent out by patients organizations (Ung med Psoriasis or Psoriasisförbundet) or through direct contact with patients visits in dermatology department (n = 15).

Inclusion criteria:

Psoriasis skin disease. Self-reported experience of Koebner phenomena. Age 18 years or older. Ability to comprehend study information. Signed and dated informed consent.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
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
否

入选标准

  • •Self reported Koebner
  • •Diagnosis of skin psoriasis

排除标准

  • •Systemic immunomodulatory treatment (including narrowband UVB)

研究组 & 干预措施

Koebner induction

Experimental

Koebner will be induced on area 22mm in diameter on upper bilateral arms and anterior bilateral thighs.

干预措施: Tape-stripping (Other)

结局指标

主要结局

Positive Koebner Phenomena (K+)

时间窗: 7-21 days after induction

Psoriasis lesion develops at site of provocation/induction

Negative Koebner Phenomena (K-)

时间窗: 21 days after induction

No psoriasis lesion develops at site of provocation/induction

次要结局

  • Stratum corneum proteomics(At baseline and at time of K+ assessment or day 21 if K-)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Albert Duvetorp

Principal Investigator

Skane University Hospital

相似试验