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临床试验/ACTRN12613000158763
ACTRN12613000158763进行中(未招募)2 期

Evaluation treatment efficacy of citalopram, synbiotic, and mebeverine for children with functional abdominal pain; a randomized, placebo-controlled study.

Isfahan University of medical silences0 个研究点目标入组 200 人开始时间: 2013年2月11日最近更新:

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
200

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
6 Years 至 18 Years(—)
性别
All

入选标准

  • Children between 6 to 18 years old, having functional abdominal pain according to ROME III criteria, having not consumption of probiotics and antibiotics in previous 2 months

排除标准

  • Having gasterointestinal problems rather than functional abdomainal pain,
  • Patients who will not use three tablets

研究者

发起方
Isfahan University of medical silences

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