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临床试验/KCT0008687
KCT0008687招募中Unknown

A prospective observational study on the effectiveness of ANI and SPI as a measure of pain in patients undergoing cystoscopic procedure under remifentanil infusion

Inje University Sanggye Paik Hospital0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
招募中
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18(Year) 至 o Limit(—)
性别
All

入选标准

  • Adult patients (> 18 years) undergoing cystoscopic procedure under monitored anesthetic care (remifentanil infusion)

排除标准

  • - ASA physical status class 5
  • - Morbid obesity ( BMI =, >35)
  • - Severe valvular heart disease
  • - Arrhythmia such as atrial fibrillation
  • - History of cardiac transplantation, Patients with cardiac pacemaker
  • - CNS disorder, autonomic disease
  • - Cognitive disorder including deliruim, dementia
  • - Patients taking alpha-2 agonist, beta blockers, or antiarrhythmics
  • - Patients chronically taking sedative hypnotics and narcotic analgesics
  • - Patients who underwent nerve block for pain control
  • - emergency surgery
  • - Patients with mean BP below 60 mmHg and heart rate below 45 bpm and above 120 bpm on the morning of surgery
  • - in case that investigators judge that it is inappropriate to participate in this study

研究者

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