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临床试验/NCT02558621
NCT02558621已完成不适用

Clinical Trial on Performance and Acceptance of a New Robotic Assistance System During Spinal Fusion Surgery

KB Medical SA4 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2015年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24
试验地点
4
主要终点
clinical acceptance of the performance of the AQrate Robotic Assistance System.

研究概览

简要总结

The main objectives of the study are to evaluate the acceptance into operating flow, performance and safety of the AQrate Robotic Assisted System during the spinal fusion surgery

详细描述

Based on the literature review of similar devices and on the pre-clinical tests performed with the AQrate System on bench and cadavers, the study is build around the following hypothesis:

  1. The design and principle of operation of the AQrate System permits a correct integration in the surgical procedure flow thus enabling the surgeon to benefit from its advantages while not generating any additional operational difficulties
  2. The stability and ease of use of the device will permit the surgeon to achieve any planned spinal fusion without requiring additional assistance from the medical staff compared to a conventional spinal fusion surgery.
  3. A spinal fusion surgery procedure that is performed with the use of the AQrate System is similar to conventional spinal fusion surgery. If correctly used, no additional adverse event should be observed.
  4. The exposure to x-ray should decrease as the need of intraoperative recheck of pedicle screws placed should be reduced
  5. The precision of placement of pedicle screw should not be adversely affected by the use of the system compared to conventional spinal surgery.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients (age from 18 years to 85 years) scheduled for spinal fusion surgery,
  • Primary spinal surgery (It is the first surgery on this patient's spine)
  • Patient is capable of complying with study requirements, and
  • Patient is willing to provide a signed informed consent.

排除标准

  • Pregnancy and lactation
  • Simultaneous participation in other clinical studies
  • Infection or malignancy
  • Previous spondylodesis
  • Previous spinal surgical procedures
  • Neurologic diseases (e.g. Charcot-Marie Tooth, Guillain-Barre syndrome, cerebral palsy, neurofibroma)
  • Spinal cord abnormalities with any neurologic symptoms or signs
  • Paraplegia
  • Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study.
  • Patient cannot follow study protocol, for any reason
  • Patient cannot or will not sign informed consent
  • Patients in emergency situation, are not legally competent, cannot understand the situation,
  • Pediatric patients

结局指标

主要结局

clinical acceptance of the performance of the AQrate Robotic Assistance System.

时间窗: Day of surgery

The acceptance of the performance of the AQrate System will be measured by scale given to total of 8 questions.

次要结局

  • Accuracy of spinal screws placed(Within one month of surgery)
  • Intraoperative exposure to radiation(Day of surgery)

研究者

发起方
KB Medical SA
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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