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

Not Applicable

• Conditions: Robot-assisted surgery, including urological, general, gynaecological, and thoracic laparoscopic surgical procedures; Surgery

• Registration Number: ISRCTN49651854
• Lead Sponsor: CMR Surgical Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-01
• Last Update Posted: 8 February 2021
• Study Completion: 2025-04-30

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 10000

Inclusion Criteria

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

Exclusion Criteria

Does not meet inclusion criteria

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intra- or post-operative complications recorded in the patient’s medical records up to 90 days post-surgery

Secondary Outcome Measures

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