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
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