Evaluation of efficacy of patency capsule for the assessment of endoscopic balloon dilatation in the small bowel stricture of Crohn's disease patients
Not Applicable
- Conditions
- Crohn's disease
- Registration Number
- JPRN-UMIN000008650
- Lead Sponsor
- Osaka University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients with ileus. 2) Allergic or intolerant to barium or lactose. 3)Pregnant or breast-feed women. 4) Patients who were considered not eligible to this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Damage and retention rate of patency capsule after the balloon dilatation.
- Secondary Outcome Measures
Name Time Method 1. Evaluation of location of patency capsule retention before balloon dilatation. 2. Diameter, number of strictures and number of balloon dilation.