Skip to content

A database to record safety information from patients who have had surgery using the Versius Surgical Robotic System

CMR Surgical Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN49651854
Enrollment
10000
Registered
2019-10-01
Start date
2019-03-02
Completion date
Unknown
Last updated
2021-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Robot-assisted surgery, including urological, general, gynaecological, and thoracic laparoscopic surgical procedures Surgery

Interventions

Current interventions as of 26/01/2021: The Versius Surgical Robotic System is licensed for use in urologic surgical procedures, general laparoscopic surgical procedures, gynaecologic

Sponsors

CMR Surgical Limited
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Any patient eligible for surgery using the Versius Surgical Robotic System as determined by their surgeon

Exclusion criteria

Exclusion criteria: Does not meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
Intra- or post-operative complications recorded in the patient’s medical records up to 90 days post-surgery

Secondary

MeasureTime frame
1. Rate of conversion to another surgical method identified during surgery 2. Operative time recorded during surgery as recorded in patient medical records 3. Length of hospital stay as measured as time from admission to date of discharge recorded in patient medical records 4. Return to OR within 24 h as recorded in patient medical records 5. Readmission to hospital within 30 days as recorded in patient medical records 6. 90-day mortality as recorded in patient medical records

Countries

France, India, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026