跳至主要内容
临床试验/EUCTR2011-006129-17-DE
EUCTR2011-006129-17-DE进行中(未招募)1 期

A randomized, double blind, placebo-controlled pilot study on the efficacy of Passiflora incarnata L. in an acute stressful situation - P. incarnata and stress - P1-2011

PASCOE Pharmazeutische Präparate GmbH0 个研究点目标入组 60 人开始时间: 2012年3月8日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
60

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, non-smoking, 25-45, BMI>19<30, signed informed consent, females: oral contraceptives
  • 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 60
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • condition or medication that could put the subject at risk or interfere with the accuracy of the study results, participation in another clinical study, ability to speak for oneself lacks or can be doubted, women: pregnant or lactating

研究者

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