Comparing robotic platforms for kidney surgery outcomes
Official title: Comparison of Outcomes of Multiple Platforms for Assisted Robotic-Kidney
Run by Azienda Ospedaliera Universitaria Integrata Verona · NCT06290427 · Data updated 2026-11-12
This study is testing which robotic system, DaVinci or Hugo, works better for kidney surgery by looking at complications and outcomes for patients with localized kidney tumors.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 90 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Azienda Ospedaliera Universitaria Integrata Verona Academic / other |
| Locations | 1 site (Verona, VR) |
| Status | Recruiting |
| Started | February 1, 2024 |
| Main results expected | December 12, 2024 |
| Study ends | June 2025 |
| Registry record updated | January 3, 2025 |
| Trial ID | NCT06290427 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 to 90 with localized kidney tumors suitable for partial nephrectomy.
✕Probably not a fit
Patients who are not suitable for partial nephrectomy or who do not meet the age criteria will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial evaluates postoperative complications associated with robotic-assisted partial nephrectomy using two surgical platforms: DaVinci and Hugo. Participants will undergo surgery with one of these platforms, and the study aims to identify differences in intra- and post-operative outcomes, including complications, oncological results, and technical aspects. The goal is to provide preliminary insights into the effectiveness and safety of these robotic systems in treating localized kidney tumors.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and reduced complications for patients undergoing robotic kidney surgery.
How similar studies have gone: Other studies have explored robotic-assisted surgeries, but this specific comparison of platforms is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * 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.
Where it's running
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Urology Unit, AOUI Verona
Verona, Vr, Italy Recruiting
Study contacts
- Principal investigator: Alessandro AA Antonelli, MD — Azienda Ospedaliera Universitaria Integrata Verona
- Study coordinator: Alessandro AA Antonelli, MD
- Email: alessandro.antonelli@aovr.veneto.it
- Phone: +39 0458127701
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Neoadjuvant HIF-2α inhibitor with or without PD-1 antibody for resectable clear cell kidney cancer
This trial tests whether casdatifan alone or combined with zimberelimab can shrink tumors in people with resectable clear cell kidney cancer before surgery.
-
R.E.C.K versus Exparel for pain control during robotic kidney removal
This will test whether intraoperative R.E.C.K or Exparel gives better pain control and reduces opioid use in adults having robotic partial or radical nephrectomy.
-
Olaparib treatment for patients with metastatic kidney cancer and specific gene mutations
This study is testing if the oral medication olaparib can help people with advanced kidney cancer who have certain gene mutations and have already tried other treatments.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.