Prospective cohort study about the treatment of constipatio
Not Applicable
- Conditions
- chronic constipation
- Registration Number
- JPRN-UMIN000037007
- Lead Sponsor
- Keio University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 1500
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with constipation due to some organic disorders
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Treatment response rates and safety between 2 and 6 weeks after the medication for chronic constipation
- Secondary Outcome Measures
Name Time Method