Versius Robotic Surgery in the NHS for soft-tissue procedures
Official title: Robotic-Assisted Surgery With Versius in the NHS: Retrospective Comparative Performance Study Across Multiple Soft-Tissue Specialties
Run by CMR Surgical Ltd · NCT07761299 · Data updated 2026-11-12
This study tests how Versius robotic-assisted surgery compares to standard surgical methods for soft-tissue procedures in routine NHS care.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 1200 (estimated) |
| Sponsor | CMR Surgical Ltd Industry-sponsored |
| Locations | 5 sites (London and 4 other locations) |
| Status | Recruiting |
| Started | September 22, 2026 |
| Main results expected | December 2027 |
| Study ends | December 2027 |
| Registry record updated | October 16, 2026 |
| Trial ID | NCT07761299 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Patients undergoing one of the predefined Versius index soft-tissue procedures, with or without laparoscopy or open approach, who can provide written informed consent (or via a legal representative if under 16).
✕Probably not a fit
Patients who have BMI 40 kg/m2 or higher, are undergoing concomitant surgeries, or are enrolled in interventional studies may not experience clear benefit from this observational evaluation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study collects real-world data on short- and long-term outcomes after Versius robot-assisted surgery versus conventional approaches across predefined soft-tissue procedures in NHS practice. It includes patients aged 16 and older (or their legal representatives for under 16) who undergo eligible procedures with Versius, laparoscopic, or open surgery. Exclusion criteria remove those in interventional trials, undergoing additional concomitant surgeries, lacking consent, or with BMI 40 kg/m2 or higher. Data will come from multiple NHS sites to generate comparative effectiveness evidence in routine clinical settings.
Why it matters
Potential benefit: If successful, the study could clarify the real-world benefits and risks of Versius robotic surgery for soft-tissue procedures, informing future practice and patient choice.
How similar studies have gone: Previous observational data on robotic-assisted procedures have shown variable but generally informative insights into safety and effectiveness in real-world NHS settings.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients undergoing one of the index procedures with Versius, laparoscopically or with open surgery. 2. Patients who provide written consent (16 years or older) or for whom an appropriate legal representative who provides written informed consent (\<16 years old). Exclusion Criteria: 1. Patients participating in an interventional clinical study that might impact the defined endpoints. 2. Patients undergoing concomitant surgery. 3. Patients or appropriate legal representatives unwilling to provide written consent. 4. Patients with BMI at or above 40 kg/m2.
Where it's running
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Watford General Hospital
Watford, United Kingdom Recruiting -
St Thomas' Hospital
London, United Kingdom Not yet recruiting -
Manchester University NHS Foundation Trust
Manchester, United Kingdom Not yet recruiting -
University Hospital Southampton NHS Foundation Trust
Southampton, United Kingdom Not yet recruiting -
Great Western Hospitals NHS Foundation Trust
Swindon, United Kingdom Not yet recruiting
Study contacts
- Principal investigator: Paul Stanciu — Watford General Hospital
- Study coordinator: Mark Slack
- Email: mark.slack@cmrsurgical.com
- Phone: +44 7766 024389
Similar studies
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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.