The study of looking for the optimal evaluation method of clinical activity by using new UC-Capsule Endoscopic Sore (UCCAS) LUCCAS study
Not Applicable
- Conditions
- lcerative colitis
- Registration Number
- JPRN-UMIN000016156
- Lead Sponsor
- Saitama Medical Center, Saitama Medical University
- 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
patients with conformed or suspicious intestinal obstruction, stenosis or fistula patients with conformed and suspicious radiation colitis patients who will not be able to perform capsule endoscopy because of the history of abdominal surgery patients treated with operation of pacemaker and/or electric device patients with confirmed and suspicious swallowing disturbance patients with pregnancy and lactation patients with the treatment of malignancy papatients defined inappropriate for the entry into this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method