Investigation of Efficacy and Safety in Robot-Assisted Laparoscopic Urologic Reconstruction Procedures.
Not Applicable
Recruiting
- Conditions
- Investigation of Efficacy and Safety in Robot-Assisted Laparoscopic Urologic Reconstruction Procedures.
- Registration Number
- JPRN-UMIN000053397
- Lead Sponsor
- Kyoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are unable or unwilling to cooperate with this study. Patients for whom laparoscopic surgery is medically contraindicated. Repair procedures for urinary tract injuries or strictures that occur or are identified during surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Outcome Measure: Surgical Success Rate Presence or Absence of Postoperative Urinary Passage Obstructions. Post-urologic reconstruction, clinical data such as details of each participant's surgery and test results will be collected from medical records. The progress will be tracked from the perioperative period up to five years postoperatively to confirm the efficacy and safety of this surgical technique.
- Secondary Outcome Measures
Name Time Method