Study to evaluate the safety and efficacy of the Versius surgical system in robot-assisted cholecystectomy (a surgical procedure to remove your gallbladder)
- Conditions
- Robot-assisted cholecystectomySurgery
- Registration Number
- ISRCTN48886202
- Lead Sponsor
- CMR Surgical (United Kingdom)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 30
1. Patient deemed suitable for laparoscopic cholecystectomy procedure using Versius Surgical Robotic System
2. Patients able to provide written informed consent to participate in the study (with help of appropriate legal representatives if required)
3. Male or female, aged 18 years or above
4. Females of childbearing potential must not be pregnant and agree to not become pregnant for the duration of the study
5. Patients with BMI <40 kg/m². Priority BMI 25 to 40 kg/m²
1. Patient participation in an investigational clinical study within 30 days before screening
2. Inability or difficulties to provide informed consent
3. Oncological cases: patients undergoing surgery or treatment for malignant disease
4. Patients who fall into the American Society of Anaesthesiologists (ASA) Class IV or above
5. History of chronic alcohol or drug abuse
6. Chronic renal failure or on dialysis
7. Significant medical history or immunocompromised
8. Subjects with any other clinically significant unstable medical disorder, life-threatening disease, or anything else in the opinion of the Investigator which would contra-indicate a surgical procedure
9. Patient tested COVID positive within the last 30 days of screening
10. Patient tested COVID positive within 48 hours of the procedure
11. Diabetes mellitus (Glycemia >11mmol/l; >200 mg/dl)
12. Uncontrolled hypertension
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method