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临床试验/KCT0006248
KCT0006248已完成未知

Comparison of bispectral index(BIS) change and clinical signs of awakening during sugammadex reversal of neuromuscular block according to the depth of propofol-remifentanil anesthesia

Samsung Medical Center0 个研究点目标入组 66 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
66

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 75(Year)(—)
性别
All

入选标准

  • 1) Patents who have American society of anesthesiologist physical status I to III
  • 2) Patients who are planned to undergo elective major abdominal surgery using propofol-remifentanil anesthesia taking one hour or more.

排除标准

  • 1) Pediatric patient at or under 18.
  • 2) Body Mass Index > 35 kg / m 2 or <18.5 kg / m 2
  • 3) Severe liver disease
  • 4) Severe kidney disease (GRF <30 or under hemodialysis)
  • 5) Neuromuscular disease or mental illness
  • 6) Those diagnosed with metabolic diseases
  • 7) Drug addiction or alcohol addiction
  • 8) Emergency surgery
  • 9) Pregnant women or nursing women
  • 10) People who have contraindications to muscle relaxants and sugammadex
  • - Patients who have allergies to drugs or have a history of hypersensitivity reactions, respiratory disease patients, arrhythmia patients

研究者

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