NCT00948870已完成不适用
Trial of Chinese Prescription Shugan Decoction on Irritable Bowel Syndrome（Diarrhea Type）
Shanghai University of Traditional Chinese Medicine1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2009年8月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Symptoms and conditions of tongue and pulse
研究概览
简要总结
The purpose of this study is to evaluate the efficacy and safety of the Chinese prescription Shugan decoction on irritable bowel syndrome（diarrhea type）.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of irritable bowel syndrome（diarrhea type）
- •Male of female patients between 18-65 years old
- •Written informed consent
排除标准
- •Discrepancy of irritable bowel syndrome
- •Diarrhea-type of irritable bowel syndrome combine with intestinal disease
- •Combined with severe heart, gallbladder, kidney, endocrine system, hemopoietic system or nervous system disease.
- •Pregnancy or breast feeding women, or unwilling to have contraception.
研究组 & 干预措施
Shugan Decoction
Experimental
干预措施: Shugan decoction (Drug)
low does of Shugan decoction
Placebo Comparator
干预措施: Shugan decoction (Drug)
结局指标
主要结局
Symptoms and conditions of tongue and pulse
时间窗: 4 weeks
次要结局
- Indicates of liver and renal function(4 weeks)
研究者
研究点 (1)
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