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临床试验/JPRN-UMIN000022282
JPRN-UMIN000022282已完成未知

The efficacy of Keishikashakuyakuto for irritable bowel syndrome - The efficacy of Keishikashakuyakuto for IBS

Yokohama City University School of Medicine Department of Gastroenterology and Hepatology0 个研究点目标入组 50 人开始时间: 2016年5月11日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1,Patients who had history of gastrointestinal tract resection 2,Patients who have severe complications 3,Patients who have history of Kampo allergies 4,Patients who have history of lactose intolerance 5,Patients who had taken new drug therapy within 4 weeks before entry 6,Patients who had any change in types, dosage, or adiministration of their prescribed drugs within 4 weeks before entry 7,Patients who are or are going to be participating in other clinical studies 8,Patients who are pregnant or possibly pregnant 9,Patients who are judged as inadequately for study entry

研究者

发起方
Yokohama City University School of Medicine Department of Gastroenterology and Hepatology

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