Comparison of efficacy and safety between MONOFIX®-PDO versus V-loc™ for resection bed suture during robot-assisted partial nephrectomy: A randomized control, multicenter, single-blinded trial
- Conditions
- Diseases of the genitourinary system
- Registration Number
- KCT0006809
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 173
? 19-85 aged men and women
? Clinical stage T1-2N0M0
? ECOG PS 0-1
? Patients scheduled for robotic partial nephrectomy
? Patients who read consent and can voluntarily give consent
? When it is expected that suture of the resected surface is not necessary after resection
? Those who have received pre-operative chemotherapy, targeted therapy, immunotherapy, etc.
? Previous intraperitoneal surgery or radiotherapy history
? Patients inadequate to participate in clinical trials due to comorbid diseases such as moderate to moderate cardiovascular disease, cerebrovascular disease, respiratory or liver disease
? Uncontrolled infectious disease
? Uncontrolled bleeding tendency
? Any other person judged by the investigator that participation in clinical trials is inappropriate
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method resection bed suture time
- Secondary Outcome Measures
Name Time Method Total usage time of suture;Warm ischemic time;Total console time;estimated blood loss;Transfusion during or after surgery;Hemoglobin difference before and after surgery;Hemoglobin reduction on day 1 after surgery;Postoperative complications;Serious complications after surgery