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临床试验/EUCTR2009-013426-16-GB
EUCTR2009-013426-16-GB进行中(未招募)1 期

Management of Irritable Bowel Syndrome in Primary Care: Feasibility randomised controlled trial of mebeverine, methylcellulose, placebo and a patient self-management cognitive behavioural therapy website. (MIBS Trial) - Management of Irritable Bowel Syndrome in Primary Care: RCT (MIBS)

niversity of Southampton0 个研究点目标入组 150 人开始时间: 2009年10月23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)
发起方
入组人数
150

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

入选标准

  • Patients aged 16 to 60 yrs with symptoms of irritable bowel syndrome that fulfil the Rome III criteria.
  • Are the trial subjects under 18? yes
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Atypical symptoms – (unexplained weight loss, rectal bleeding), diagnosis of inflammatory bowel disease, coeliac disease, peptic ulcer disease, porphyria, pregnant or breast feeding, currently taking or allergy to mebeverine or methylcellulose. If patients are already taking mebeverine or methlycellulose but are keen to enter the trial they will be able to do so if they fulfil the inclusion criteria, do not meet any of the other exclusion criteria and they undertake a 4 week mebeverine and methylcellulose free wash out period before entering the trial.

研究者

发起方
niversity of Southampton

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