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临床试验/IRCT20210427051098N3
IRCT20210427051098N3招募中3 期

Evaluating the effect of Valerian (Valeriana officinalis) supplementation on the symptoms severity and quality of life in patients with irritable bowel syndrome: A randomized and double-blind clinical trial

Yazd University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
50

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
25 years 至 65 years(—)
性别
All

入选标准

  • 1- Age 25 to 65 years
  • 2- Patients with irritable bowel syndrome according to the diagnosis of a gastroenterologist according to ROME-IV criteria

排除标准

  • Dietary changes during the study
  • Unwillingness to continue attending the study
  • Pregnancy or breastfeeding during the study
  • Hospitalization
  • Suffering from certain diseases such as any active stomach-enteric disease or taking certain medicines
  • Having an allergy to herbal products

研究者

发起方
Yazd University of Medical Sciences

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