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临床试验/ACTRN12619001461189
ACTRN12619001461189已完成未知

nderstanding the calming effect of passionflower in healthy people

Massey University0 个研究点目标入组 91 人开始时间: 2019年10月22日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
91

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
All

入选标准

  • Healthy adults between 18 and 45 years of age will be eligible for this study. Proficiency in English will be a requirement for participants (due to the nature of outcome assessment tools).

排除标准

  • have psychiatric disorders (including psychotic or bipolar disorder illness, major depressive disorder, or any specific anxiety disorder),
  • have had either substance abuse or dependency disorder in the previous six months, including alcohol
  • are currently using antidepressants, mood stabilisers, antipsychotics, opioid, or analgesics
  • are diagnosed with known abnormal liver function and/or inflammatory diseases
  • have experienced adverse reactions to passionflower or any active ingredients of study materials
  • have regularly used passionflower in the previous 12 months
  • have had more than one occasion of passionflower use each week over the past month
  • are pregnant or trying to conceive
  • are breastfeeding
  • are regular smokers (more than one cigarette per week)
  • are unable to comply with the abstention of caffeinated products and exercise for two hours and alcohol for a minimum of 12 hours prior to visits

研究者

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