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Robotic vs Open Nephrectomy for ADPKD (ADPKDR-O)

U

University of Bologna

Status

Active, not recruiting

Conditions

Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Study type

Observational

Funder types

Other

Identifiers

NCT07355114
ADPKDR-O

Details and patient eligibility

About

The goal of this observational prospective cohort study is to evaluate the feasibility, safety, and postoperative outcomes of robotic-assisted unilateral native nephrectomy using the Medtronic Hugo™ RAS system compared with the open surgical approach in patients with autosomal dominant polycystic kidney disease (ADPKD)

The main question(s) it aims to answer are:

Is robotic-assisted unilateral nephrectomy with the Hugo™ RAS system feasible and safe in patients with ADPKD? Does robotic-assisted nephrectomy provide comparable or improved postoperative outcomes (e.g., complications, transfusion rates, length of hospital stay) compared with open nephrectomy? Researchers will compare robotic-assisted unilateral nephrectomy (Hugo™ RAS) with open unilateral nephrectomy to see if the robotic approach results in similar morbidity with shorter hospital stay, despite longer operative times.

Participants are adult patients with ADPKD undergoing unilateral native nephrectomy at a single tertiary transplant center, most of whom have end-stage renal disease and are candidates for or recipients of kidney transplantation. Both male and female patients were included; patients undergoing bilateral nephrectomy were excluded.

Enrollment

57 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult Patients who underwent unilateral nephrectomy for ADPKD

Exclusion criteria

  • Patients who underwent bilateral nephrectomy for ADPKD were excluded from the study.

Trial design

57 participants in 2 patient groups

Open nephrectomy
Description:
Unilateral Nephrectomy for ADPKD
Robotic Nephrectomy
Description:
Unilateral Robotic nephrectomy for ADPKD with Hugo RAS System

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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