跳至主要内容
临床试验/NCT04352140
NCT04352140已完成不适用

Electromyographic and Acceleromyographic Monitoring in Restricted Arm Movement Surgical Setting. A Prospective, Randomized Trial.

Mayo Clinic6 个研究点 分布在 3 个国家目标入组 60 人开始时间: 2020年8月18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
Mayo Clinic
入组人数
60
试验地点
6
主要终点
Accuracy of Values Between Tetragraph and ToFscan

研究概览

简要总结

Researchers are comparing the ease of use and repeatability of the force vs electrical activity produced by a muscle after it has undergone nerve stimulation during a surgical procedure in which the patients' arm movement is restricted (placed under surgical drapes) in laparoscopic or robotic procedures.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Age > or = 18 years old
  • Patients willing to participate and provide an informed consent
  • Patients undergoing an elective laparoscopic or robotic surgical procedure that requires use of NMBA agents administered intraoperatively.

排除标准

  • Patients with disorders, such as stroke, carpal tunnel syndrome, broken wrist with nerve damage, Dupuytren contracture, or any similar wrist injury.
  • Patients with systemic neuromuscular diseases such as myasthenia gravis
  • Patients with significant organ dysfunction that can significantly affect pharmacokinetics of neuromuscular blocking and reversal agents, i.e., severe renal impairment or end-stage liver disease.
  • Patients having surgery that would involve prepping the arm or leg into the sterile field

结局指标

主要结局

Accuracy of Values Between Tetragraph and ToFscan

时间窗: Up to 1 hour postoperatively

The number of subject's who's residual neuromuscular blockage units are the same on both the TetraGraph and the ToFscan

次要结局

  • Incidence of Residual Neuromuscular Blockade(Up to 1 hour postoperatively)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

J. Ross Renew, M.D.

Principal Investigator

Mayo Clinic

研究点 (6)

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