A study examining the safety and efficacy of robot-assisted surgery using the da Vinci Si system for patients with ureteropelvic junctionpart stenosis
Not Applicable
- Conditions
- reteropelvic junctionpart stenosis
- Registration Number
- JPRN-UMIN000035800
- Lead Sponsor
- Juntendo University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
Patient who the research director judged unsuitable as a subject
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adverse event occurrence rate: presence or absence of complications at approach, intraoperative or postoperative. Transition to laparotomy or laparoscopic surgery, blood transfusion practice, organ damage, vascular injury, postoperative bleeding, postoperative infection, pulmonary infarction, gas embolism.
- Secondary Outcome Measures
Name Time Method Surgical results: operation time, bleeding volume Postoperative course: postoperative Vital Sign, urine volume, body temperature, drainage volume, leukocytes / CRP values on days 1, 3 and 5 postoperatively, postoperative pain (VAS: Visual Analog Scale), hospitalization period Pathological examination: presence or absence of malignancy in resected bile duct Overall survival period: existence of death, period from surgery to death