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临床试验/NCT04352127
NCT04352127已完成不适用

Comparison of Visual and Electromyography Assessments in Response to Train-of-Four Stimulation of the Ulnar Nerve

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2020年8月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
55
试验地点
1
主要终点
Subjective Evaluation to Neurostimulation

研究概览

简要总结

Researchers are comparing the accuracy of measuring muscle relaxation during and after surgery with a device that provides numeric value versus visual observation to count of muscle twitches or absence of them by a medical provider monitoring your anesthesia during surgery.

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
Double (Participant, Care Provider)

入排标准

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

入选标准

  • •Age > or = 18 years old
  • •Patients willing to participate and provide an informed consent
  • •Patients undergoing an elective 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

研究组 & 干预措施

Dominant hand

Experimental

Subject scheduled to undergo an elective surgical procedure will have TetraGraph device lead placement on the dominant hand and routine clinical monitor on non-dominant hand

干预措施: TetraGraph (Device)

Non-dominant hand

Experimental

Subject scheduled to undergo an elective surgical procedure will have TetraGraph device lead placement on the non-dominant hand and routine clinical monitor on dominant hand

干预措施: TetraGraph (Device)

结局指标

主要结局

Subjective Evaluation to Neurostimulation

时间窗: up to 1 hour postoperatively

The percentage of subjective evaluations that overestimated the response of the adductor pollicis muscle following neurostimulation of the ulnar nerve when compared to objective measurements.

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 (1)

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