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临床试验/KCT0005749
KCT0005749尚未招募未知

The comparison of respiratory depression between propofol and propofol in combination with dexmedetomidine for deep sedation during total knee replacement under spinal anesthesia: a prospective randomized controlled trial

The Catholic University of Korea, Daejeon St. Mary's Hospital0 个研究点目标入组 82 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
82

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
50(Year) 至 80(Year)(—)
性别
All

入选标准

  • American society of anesthesiology (ASA) physical status 1, 2, 3
  • Age: 50-80 yrs
  • Patients for total knee replacement surgery under spinal anesthesia

排除标准

  • Severe bradycardia, HR <50 ?/min
  • Severe cardiopulmonary disease, ASA 4??
  • Severe hepatic or renal disease
  • Body mass index > 35
  • contraindication to spinal anesthesia
  • Allergy to study medicine, propofol, dexmedetomidine
  • History of severe obstructive sleep apnea or a tendency for airway obstruction
  • Refusal of intraoperative sedation

研究者

发起方
The Catholic University of Korea, Daejeon St. Mary&#39;s Hospital

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