跳至主要内容
临床试验/ISRCTN30654050
ISRCTN30654050已完成不适用

A pilot study, open label, placebo controlled, non-randomised trial of the influence of Lactobacillus Shirota on anxiety and depression in patients with irritable bowel syndrome (IBS)

Yakult UK Ltd (UK)0 个研究点目标入组 40 人开始时间: 2008年9月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
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

性别
All

入选标准

  • 1. Aged between 20 and 50 years, either sex
  • 2. Diagnosis of IBS using Rome II Criteria and either moderate/severe anxiety and/or depression
  • 3. Medication on stable dosage for at least 4 weeks before entry into the study
  • 4. Demonstrates a full understanding of the study protocol and its requirements
  • 5. Demonstrates willingness to take either trial probiotic or control placebo as required in the study protocol

排除标准

  • 1. Already taking regular probiotic supplement
  • 3. Has IBS but not moderate/severe anxiety or depression
  • 4. Unstable medication
  • 5. Lactose intolerance
  • 6. Demonstrates difficulty in understanding study protocol requirements
  • 7. Does not agree to take either trial probiotic or control placebo as required in the study protocol

研究者

发起方
Yakult UK Ltd (UK)

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