A comparative study to assess the safety and efficacy of underwater EMR for intermediate size (10-20 mm) colorectal polyps.
Phase 2
- Conditions
- Sessile colorectal polys 10mm - 20mm in diameter.
- Registration Number
- JPRN-UMIN000018989
- Lead Sponsor
- Osaka international cancer institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 230
Inclusion Criteria
Not provided
Exclusion Criteria
1)pedunculated polyp 2)residual lesions after EMR 3)patients with marked electrolyte abnormality 4)patients with hematological abnormality 5)patients with severe organ failure 6) patients with inflammatory bowel disease and polyposis 7) patients who have been judged as inappropriate for this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method