Actively Recruiting
Versius Paediatrics Study
Led by CMR Surgical Ltd · Updated on 2024-10-15
150
Participants Needed
3
Research Sites
129 weeks
Total Duration
On this page
Sponsors
C
CMR Surgical Ltd
Lead Sponsor
U
University Hospital Southampton NHS Foundation Trust
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is prospective, multi-phase, single arm, multi-centre, multi-surgeon feasibility clinical trial to provide proof of concept and clinical evidence regarding the safety and efficacy of Versius (robotic surgery medical device) in Urological Procedures in Paediatric population. In alignment with IDEAL (Idea, Development, Exploration, Assessment, Long-term study) Framework, this study will consist of 3 main phases to ensure proper procedure development while ensuring patients safety. Feasibility and safety will be assessed on an ongoing basis, and specifically after completion of the first 3 procedures, at a single site (Southampton/Lead), each conducted one week apart to allow the identification of unanticipated risks/adverse events. Once deemed safe, based on the results of the 3 cases enrolled in Phase I, 7 further cases would be completed, at the same site. Once the procedure is deemed safe according to safety data collected, the recruitment will proceed to full trial patient accrual, 140 additional cases from the 3 participating study sites.The study patient population is children and adolescents under the age of 18, which will be provided clinical care and follow-ups per standard of care and hospital's policy.
CONDITIONS
Official Title
Versius Paediatrics Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients under 18 years old with written consent from an appropriate legal representative
- Suitable patient and disease factors for minimal access urological surgery
- Multidisciplinary team decision to treat with surgery
- Patients under the care of the pediatric urology team at a participating center
You will not qualify if you...
- Patients 18 years old or older
- Legal representative unwilling to provide written consent
- Medical contraindication for general anesthesia
- Medical contraindication for laparoscopic procedure
- Active pregnancy in post-pubertal female patients
- Morbid obesity with BMI 40 kg/m2 or higher
- Participation in another interventional clinical study affecting this study's results
- Prior pelvic or abdominal radiotherapy
- Other unstable medical disorders or life-threatening diseases that contraindicate surgery per investigator opinion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Department of Paediatric Urology, Evelina London Children's Hospital
London, United Kingdom, SE17EH
Not Yet Recruiting
2
Department of Paediatric Urology Royal Manchester Children's Hospital
Manchester, United Kingdom, M139WL
Not Yet Recruiting
3
Department of Paediatric Urology Southampton Children's Hospital
Southampton, United Kingdom, SO166YD
Actively Recruiting
Research Team
M
Mark Slack, MD
CONTACT
M
Morad Nakhleh, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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