Actively Recruiting
Comparison of Outcomes Using DaVinci and Hugo Robotic Platforms for Assisted Robotic Partial Nephrectomy in Renal Carcinoma
Led by Azienda Ospedaliera Universitaria Integrata Verona · Updated on 2025-01-03
30
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers at the Urology Unit of AOUI Verona are conducting a study to evaluate postoperative complications in patients undergoing robotic partial nephrectomy (RAPN) for localized kidney tumors. The study focuses on comparing two robotic surgery platforms: the DaVinci Surgical System and the Hugo RAS System. It aims to investigate differences in intra- and postoperative complications, as well as oncological, functional, technical, and economic outcomes between these two approaches. Participants will be assigned to one of two groups based on the surgical platform used for their partial nephrectomy: either the DaVinci RAPN or the Hugo RAS RAPN. Both interventions involve robot-assisted surgery aimed at removing part of the kidney affected by cancer while preserving healthy tissue. The study does not specify further treatment or dosing details beyond these surgical procedures. During the study, researchers will monitor participants for postoperative complications over the first four days after surgery. They will record the number of patients experiencing any complications, moderate to major complications, and major complications specifically. Participants are expected to comply with scheduled follow-up assessments and consent to the monitoring program. The study focuses on measuring safety and surgical outcomes within this immediate postoperative period.
CONDITIONS
Official Title
Comparison of Outcomes of Multiple Platforms for Assisted Robotic-Kidney (COMPAR-K)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged between 18 and 90 years old
- Patient with localized kidney tumor suitable for partial nephrectomy
- Patient able to understand and sign the informed consent
- Patient compliance with the follow-up program
You will not qualify if you...
- Patient who do not fall within the inclusion age range
- Patient not suitable for partial nephrectomy
- Patient unable to understand and sign the informed consent
- Patient unable to follow the monitoring program
- Patient refusal to participate to the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Urology Unit, AOUI Verona
Verona, VR, Italy, 37126
Actively Recruiting
Research Team
A
Alessandro AA Antonelli, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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