跳至主要内容
临床试验/EUCTR2007-006272-11-DE
EUCTR2007-006272-11-DE进行中(未招募)不适用

Validation of Dermatophot for the assessment of steroid induced skin atrophy - Validel

J.W. Goethe University Hospital0 个研究点目标入组 36 人开始时间: 2008年4月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
36

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Inclusion criteria
  • Healthy volunteers male/female age 18-60
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Exclusion criteria
  • Clinical conditions that according to investigator can interfere with the Dermatophot evaluation (e.g., generalized erythroderma such as the genetic condition Netherton’s syndrome, other skin conditions such as atopic dermatitis, psoriasis)
  • History of malignancy of any organ system, treated or untreated, within the past 5 years whether or not there is evidence of local recurrence or metastases
  • Systemic immunosuppression
  • Clinical signs of infection in the treatment area (e.g. viral, bacterial, fungal or specific skin disorders)
  • History of hypersensitivity to investigated substances to drugs with similar chemical structures and/or to any other ingredients of the formulation
  • Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG test. Females of childbearing potential and not practicing a medically approved method of contraception during and up to at least 4 weeks after the end of treatment. ‘Medically approved’ contraception may include implants, injectables, combined oral contraceptives, IUDs, but also abstinence at the discretion of the investigator
  • Use of other investigational drugs within 30 days of enrolment

研究者

发起方
J.W. Goethe University Hospital

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