VOLARE, v1

  • Research type

    Research Study

  • Full title

    VOLARE - Versius Or Laparoscopic Abdominal hernia REpair. A single blinded randomised controlled trial comparing the ergonomics of laparoscopic and Versius robotic assisted abdominal hernia surgery

  • IRAS ID

    311109

  • Contact name

    Frances Dixon

  • Contact email

    Frances.dixon@mkuh.nhs.uk

  • Sponsor organisation

    Milton Keynes University Hospital NHS Foundation Trust

  • Clinicaltrials.gov Identifier

    NCT05253586

  • Duration of Study in the UK

    2 years, 0 months, 1 days

  • Research summary

    This is a study comparing abdominal hernia surgery done via conventional keyhole (laparoscopic) surgery with robotic-assisted keyhole surgery, using the Versius robotic system. Our main objective is to assess the physical strain of both types of surgery on the operating surgeon, but we will also collect data on the patient outcomes and teamwork. This will be used to guide the design of a larger scale trial in future.

    Robotic-assisted surgery is increasing in its use in general surgery, as it is thought that the instruments give more precision and stability for complex operations. There is no automation and the robot is under the surgeon's control at all times. Because the surgeon sits at a control console instead of standing by the bedside, robotic-assisted surgery may be better for the surgeon in terms of physical strain. Chronic pain and long-term injuries are common amongst surgeons and so this is an important area of investigation.

    To assess physical strain we will use photographs of the operating surgeon and will measure joint position using a scale called Rapid Entire Body Assessment. We will assess mental strain using a questionnaire, and will record video of the surgical team to look at overall team functioning during the operation.

    Any patients who are having abdominal hernia repair surgery (and who are suitable for keyhole surgery) may potentially be suitable to take part in this trial. The participant will not know whether they have had robotic or normal keyhole surgery. There will be no additional hospital visits or invasive tests associated with being in this study, but participants will need to complete 2 questionnaires twice. Robotic-assisted surgery is currently used within the NHS and it is known to be a safe treatment option.

  • REC name

    South Central - Oxford A Research Ethics Committee

  • REC reference

    22/SC/0096

  • Date of REC Opinion

    7 Jun 2022

  • REC opinion

    Further Information Favourable Opinion