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Versius Or Laparoscopic Abdominal Hernia REpair — VOLARE  

Abdominal Surgery Clinical Trial

Official title:
A Single Blinded Randomised Controlled Trial Comparing the Ergonomics of Laparoscopic and Versius Robotic Assisted Abdominal Hernia Surgery

Clinical Trial Summary

This trial will compare laparoscopic and robotic-assisted abdominal hernia repairs, using the Versius® system. We will initially aim to recruit 60 patients (20 patients in the laparoscopic arm and 40 in the robotic arm) in order to assess the ergonomic impact of each modality on the operating surgeon. This aims to provide in vivo information on whether robotic surgery provides any advantages to the operating surgeon. This trial will also be used to assess the feasibility of recruitment to a future larger study, and any data collected will be used as pilot data.

Clinical Trial Description

This study has been designed to assess the ergonomics of Versius® assisted surgery in comparison with laparoscopic surgery in the management of abdominal hernias. The study will randomise 60 patients who require repair of an abdominal hernia and have been deemed suitable for a minimally invasive approach. Patients will be randomised to receive either laparoscopic or Versius® robotic assisted surgery but will be informed that it will be attempted via a minimally invasive approach that could include either of these two subtypes of minimally invasive surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05253586
Study type Observational
Source Milton Keynes University Hospital NHS Foundation Trust
Contact Joanne Turner
Phone +441908995136
Email joanne.turner@mkuh.nhs.uk
Status Not yet recruiting
Phase
Start date March 31, 2024
Completion date March 31, 2024
View Details
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