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临床试验/EUCTR2004-004466-33-DE
EUCTR2004-004466-33-DE进行中(未招募)不适用

doubleblind (observer blind), placebo-controlled, clinical-experimental study phase II in order to examine the local compatibility of Dr. Theiss Ringelblumen Salbe N by the duhring-chamber-test and in a open user trial - local compatibility test and open user trial with Dr. Theiss Ringelblumen Salbe

Dr. Theiss Naturwaren GmbH0 个研究点目标入组 40 人开始时间: 2006年1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)
入组人数
40

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

  • •written informed consent written informed data protection healthy subjects with healthy normal skin conditions age more than 18 years
  • •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

  • •Volunteers who do not fulfill any of the above described criteria Volunteers who are pregnant or breast feeding Skin irritation or disease Skin dieseases or dermatological disorders Volunteeers with severe disorders Topical medication in the test areas Participation in an study in the last 4 weeks Consumption of alcohol or drugs

研究者

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