Safety and efficacy of Hange-shashin-to therapy for refractory pouchitis
Phase 1
- Conditions
- pouchitis
- Registration Number
- JPRN-UMIN000010004
- Lead Sponsor
- Department of lower gastroenterological surgery, Hyogo college of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
1)Concomitant administrations of antibiotics within 2weeks. 2)Concomitant administrations of Chinese medicine within 2weeks. 3) A patient, who is pregnant, may be pregnant, breast-feeds or hopes to be pregnant in the study period. 4) A patient who is determined as ineligible for a subject in this study by a doctor in charge or others.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Efficacy of treatment was defined Pouchitis Disease Activity Index score with each parameter which includes clinical symptoms, endoscopic appearance, and histopathological findings. These parameters were assessed at before and after treatment.
- Secondary Outcome Measures
Name Time Method