ISRCTN11414606
Active, not recruiting
Phase 2
Prospective clinical study to evaluate the safety and efficacy of the versius surgical system in robot-assisted total hysterectomy
CMR Surgical (United Kingdom)0 sites30 target enrollmentNovember 3, 2022
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Robot assisted total hysterectomy
- Sponsor
- CMR Surgical (United Kingdom)
- Enrollment
- 30
- Status
- Active, not recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patient deemed suitable for total laparoscopic hysterectomy 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\. Female, aged 18 years or above
- •4\. Female of childbearing potential, must not be pregnant
- •5\. Patients with BMI \=40 kg/m². Ideally BMI \=25 to \=40 kg/m²
Exclusion Criteria
- •1\. Patient participation in an investigational clinical study within 30 days before screening
- •2\. Inability or difficulties to provide informed consent
- •3\. Uncontrolled hypertension (\=/\>Systolic: 180 mmHg/Diastolic: 120 mmHg)
- •4\. Diabetes mellitus (Glycemia \>11mmol/L; \>200 mg/dL)
- •5\. Oncological cases, patients undergoing surgery or treatment for malignant disease
- •6\. Patients who fall into American Society of Anaesthesiologists (ASA) Class IV or above
- •7\. Uterus size of \>14 weeks
- •8\. History of chronic alcohol or drug abuse
- •9\. Chronic renal failure or on dialysis
- •10\. Significant medical history or immunocompromised
Outcomes
Primary Outcomes
Not specified
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