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临床试验/EUCTR2004-002767-25-DE
EUCTR2004-002767-25-DE进行中(未招募)不适用

Clinical trial on the efficacy of Calendula-Echinacea Ointment in sodium lauryl sulphate irritation test. A monocentric, randomised, placebo-controlled double blind clinical trial.

WALA Heilmittel GmbH0 个研究点开始时间: 2005年4月12日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)

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

  • - healthy male and female volunteers from age 18 to 65
  • - no manifest skin diseases
  • - written consent to participation in the study after detailed information
  • - willingness to follow investigator instructions
  • - for women of childbearing potential: negative pregnancy test and effective method of birth control
  • 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

  • - infectious diseases
  • - serious state of health
  • - alcohol- or drug abuse
  • - participation in other clinical trials during the last four weeks or simultaneously to the current investigation
  • - concomitant use of cortocosteroids, antihistamines, medication with anti-inflammatory or antibiotic effect or psycho-drugs
  • - manifest skin diseases
  • - manifest inflammations
  • - known allergy to one of the components of the IMP or composite flowers
  • - pregnancy or nursing

研究者

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