跳至主要内容
临床试验/NCT03452163
NCT03452163终止不适用

Performance Assessment of the Physiological Monitor Device (PMD-200), a Novel Pain Monitor, in Subjects at Neurointensive Care Unit (NICU).

Medasense Biometrics Ltd1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2018年3月8日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
3
试验地点
1
主要终点
Correlation between changes in the nociception levels of the subject (NoL Index value) prior and following a noxious stimuli

研究概览

简要总结

Performance Assessment of the PMD-200, a Novel Pain Monitor, in Subjects at Neurointensive Care Unit.

详细描述

The proposed study is design to further demonstrates the performance of the Nociception Level (NoL) Index in neurological impaired anesthetized patients under general anesthesia, by evaluating its response to controlled changes in the levels of noxious stimuli/analgesia, and to correlate the NoL response to the EEG derived pain score. Validating the performance of the NoL Index may provide a tool to monitor the pain/nociception in this population.

In this study, the PI plan to demonstrate that the NoL Index is a continuous index. It is anticipated that a higher level of nociception will correspond to a higher NoL index. On the other hand, it is anticipated that higher levels of analgesic agent for the same noxious stimulus will lead to a lower NoL index.

The participants will be monitored as in a typical ICU and according to the local guidelines by various types of monitoring devices, such as: vital signs, pulse oximeter, Bispectral Index (BIS), Electroencephalography (EEG) etc.

研究设计

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

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years old.
  • The subject is under general anesthesia
  • The subject have a blood pressure measurement (either arterial or cuff) during the study
  • A signed Informed Consent Form (ICF) has been obtain

排除标准

  • The subject is constantly agitate or moving a lot

结局指标

主要结局

Correlation between changes in the nociception levels of the subject (NoL Index value) prior and following a noxious stimuli

时间窗: Through study completion, about one year

To demonstrate that the NoL Index is correlates with changes in the nociception levels of the subject prior and following a noxious stimuli.

次要结局

  • Correlation between the NoL index and the EEG derived pain score(Through study completion, about one year)
  • Correlation between changes in the nociception levels of the subject (NoL Index value) to other nociception predictors (HR, NIBP)(Through study completion, about one year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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