A retrospective study evaluating the risk factors of the post-procedural adverse events after the treatment of superficial non-ampullary duodenal epithelial tumors.
Not Applicable
Recruiting
- Conditions
- superficial non-ampullary duodenal epithelial tumors
- Registration Number
- JPRN-UMIN000035478
- Lead Sponsor
- TT Medical Center Tokyo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with severe complications who were unable to tolerate surgery (e.g., severe heart/kidney/lung/liver disease) 2. Patients in disagreement with informed consent 3. Others
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Risk factors of the post-procedural adverse events
- Secondary Outcome Measures
Name Time Method Complete resection rate, R0 resection rate, procedure time, complication rate (delayed-perforation, delayed-bleeding)