Feasibility study investigating the efficacy and safety of SOUTEN snare for colorectal endoscopic submucosal dissectio
Not Applicable
- Conditions
- Colorectal adenoma/early colorectal cancer
- Registration Number
- JPRN-UMIN000034299
- Lead Sponsor
- TT Medical Center Tokyo Department of Gastroenterology
- Brief Summary
Among 137 neoplasms, SOUTEN-ESD was completed in all cases. No cases required conversion to hybrid ESD or to a dedicated ESD device. The mean procedure time was about 26 minutes. The en-bloc resection rate was 100% and the R0 resection rate was 100%. The rate of perforation was 0%, the rate of delayed bleeding was 2.2%, and the rate of post-ESD coagulation syndrome (PECS) was 2.9%.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 119
Inclusion Criteria
Not provided
Exclusion Criteria
Patients whose lesions were found to be outside the guideline or expanded criteria for ESD by the endoscopic characteristics and histological findings of biopsy specimens. Patients in disagreement with informed consent
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method