跳至主要内容
临床试验/ISRCTN48886202
ISRCTN48886202进行中(未招募)2 期

Prospective clinical study to evaluate the safety and efficacy of the Versius surgical system in robot-assisted cholecystectomy

CMR Surgical (United Kingdom)0 个研究点目标入组 30 人开始时间: 2023年4月13日最近更新:

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 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

排除标准

  • 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

研究者

发起方
CMR Surgical (United Kingdom)

相似试验

Study to evaluate the safety and efficacy of the... | 临床试验