EUCTR2011-004953-17-DE进行中（未招募）不适用
Measurement of epidermal and dermal thickness under therapy with Pimecrolimus 1 % Creme (Elidel® 1 % Creme), Hydrocortisonacetat 1 % Creme (Hydrogalen® Creme), Betamethasonvalerat 0,1 % Creme (Betagalen® Creme), Methylprednisolonaceponat 0,1 % Creme (Advantan® Creme), Dermatop® Basecreme and without therapy by optical coherencetomography (OCT) and 20-MHZ-ultrasound.
Technical university Dresden0 个研究点开始时间: 2011年12月9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
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
- •- age 18-40 years
- •- health volunteers
- •- normal dermis
- •- written accordance of the test person
- •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 30
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- pregnant or nursing woman,
- •- missing contraception,
- •- external or systemic therapy in the last 6 months with special drugs (Retinoids, Glucocorticoisteroids, Calcineurininhibitors,..)
- •- disease of the epidermis (atopic dermatitis, psoriasis, erythrodermie,...), skin disease who makes topical application of cremes impossible
- •- intensive UV-exposition or UV-therapy within the last 4 weeks or in trial,
- •- simultaneous participance in other clinical studies and participation in a second trial within the last 30 days
- •-hypersensitivity against Elidel®, Hydrogalen® Creme, Betagalen® Creme, Advantan® Creme, or Dermatop® Basecreme,
- •- disease with anticipate a therapy with Elidel®, Betagalen® Creme, Ecural® Fettcreme, Hydrogalen® Creme, Advantan® Creme or Dermatop® Basecreme,
- •- use of immunsuppressive drugs, or severe systemic disease,
- •- non-compliance,
- •-vaccination within the last 14 days
研究者
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