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临床试验/NCT01084031
NCT01084031已完成不适用

Dose Titration of Propofol for Tracheal Intubation in Children With Sevoflurane Inhalation Induction

Yonsei University0 个研究点目标入组 50 人开始时间: 2009年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
50
主要终点
Assessment of intubation conditions

研究概览

简要总结

Dose titration of propofol for tracheal intubation in children with sevoflurane inhalation induction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Supportive Care
盲法
Double (Participant, Investigator)

入排标准

年龄范围
6 Months 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Pediatric patients scheduled for elective day case surgery were enrolled.

排除标准

  • History of obstructive sleep apnea
  • Evidence of cardiorespiratory disease
  • Those who were obese or allergic to any of the anesthetic agents in this study
  • Those with an anticipated difficult airway, full stomach
  • History of malignant hyperthermia or other myopathy were excluded.

研究组 & 干预措施

propofol

Experimental

干预措施: propofol (Drug)

结局指标

主要结局

Assessment of intubation conditions

时间窗: 30 minutes after the surgery

Assessment of intubation conditions (vocal cord, intubation condition, cough, movement) , peri-induction HR and BP change, post-operative agitation socre at recovery room. ED50 and ED 95 of each group by uring Dixon's up and down methods. peri -induction period -comparison of above factors among each groups (GroupA: ETSevo 3vol%, Group B: ETSevo 3.5vol%, Group: ET Sevo 4vol%)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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