JPRN-jRCT2052200025已完成2 期
An exploratory Investigator Initiated clinical trial for the development of PMS-1, a device for objectively monitoring the efficacy of analgesics on postoperative pain
akai Kunihiro0 个研究点目标入组 30 人开始时间: 2020年6月8日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 30
研究概览
简要总结
The PS measured by the Pain Management System PMS-1 correlated with the amount of change in the NRS and VAS measurements, which are commonly used to measure and evaluate pain in daily practice, and could be used as an indicator to monitor the efficacy of analgesics for postoperative pain. In addition, it was confirmed that patients scheduled to undergo surgery under general anesthesia were the target patients for whom the pain performance evaluation of the device concerned could be appropriately conducted.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 ot applicable（—）
- 性别
- All
入选标准
- •(1) Patients 20 years or older at the time of consent acquisition
- •(2) Patients scheduled to undergo surgery under general anesthesia
- •(3) Patients with no apparent cognitive impairment
- •(4) Gender: Any
- •(5) Patients who have their own free written consent
排除标准
- •(1) Patients with known neurological disorders such as epilepsy, or patients with a history
- •(2) Patients taking narcotic analgesics
- •(3) Patients with a history of cerebral infarction and cerebral hemorrhage
- •(4) Patients with a history of other organic brain diseases
- •(5) Patients who have already been diagnosed with chronic pain
- •(6) Patients with cardiac pacemakers or electronic implants
- •(7) Patients with severe visual impairment
- •(8) Women who may be pregnant
- •(9) Patients who are judged by the investigator or the investigator to be inappropriate to participate in this clinical trial
研究者
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