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临床试验/NL-OMON43003
NL-OMON43003已完成不适用

The effect of CanChew®, cannabidiol (CBD) containing chewing gum on Irritable Bowel Syndrome - The CANdidate study

Wageningen Universiteit0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
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

入排标准

年龄范围
18 至 64(—)

入选标准

  • * Female, only when using the contraceptive pill
  • * Adults, aged 18-65
  • * IBS, diagnosed according to the Rome III criteria
  • * More than 3 moments of pain a week with a VAS-score of 4 and higher
  • * Signed informed consent

排除标准

  • * Use of SSRIs, tramadol or tramagetic
  • * History of intestinal surgery that might interfere with the outcome of the study
  • * Female patients: currently pregnant, breast-feeding or intending to become pregnant during the study, judged by the persons self
  • * Female who is not using the contraceptive pill.
  • * Are an employee of the department of Human Nutrition at Wageningen UR, or employee of Ziekenhuis Gelderse Vallei
  • * Participate in another research study
  • * Alcohol use (male more than 14 servings a week, female more than 7 servings a week)
  • * Hypersensitivity to one of the ingredients of the chewing gum
  • * Cannabis use is from 3 months before untill the end of the study not allowed
  • * Drug use (CYP2C19 and CYP3A4) metabolised; medication will be evaluated for this by the principal and medical investigator.

研究者

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