The efficacy of Keishikashakuyakuto for irritable bowel syndrome
Not Applicable
- Conditions
- Irritable bowel syndrome
- Registration Number
- JPRN-UMIN000022282
- Lead Sponsor
- Yokohama City University School of Medicine Department of Gastroenterology and Hepatology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method