Trial of Chinese Prescription Shugan Decoction on Irritable Bowel Syndrome(Diarrhea Type)
Not Applicable
Completed
- Conditions
- Irritable Bowel SyndromeTraditional Chinese Medicine
- Interventions
- Registration Number
- NCT00948870
- Lead Sponsor
- Shanghai University of Traditional Chinese Medicine
- Brief Summary
The purpose of this study is to evaluate the efficacy and safety of the Chinese prescription Shugan decoction on irritable bowel syndrome(diarrhea type).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
- Clinical diagnosis of irritable bowel syndrome(diarrhea type)
- Male of female patients between 18-65 years old
- Written informed consent
Exclusion Criteria
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Shugan Decoction Shugan decoction - low does of Shugan decoction Shugan decoction -
- Primary Outcome Measures
Name Time Method Symptoms and conditions of tongue and pulse 4 weeks
- Secondary Outcome Measures
Name Time Method Indicates of liver and renal function 4 weeks
Trial Locations
- Locations (1)
Longhua hospital
🇨🇳Shanghai, Shanghai, China