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临床试验/ACTRN12609000387224
ACTRN12609000387224已完成未知

A randomised controlled trial to assess respiratory complications following removal of a laryngeal mask (awake vs. anaesthetised) in children undergoing adeno-/tonsillectomy with a high risk of postoperative respiratory complications

Britta von Ungern-Sternberg0 个研究点目标入组 290 人开始时间: 2009年5月29日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
290

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
o limit 至 16 Years(—)
性别
All

入选标准

  • Children, aged 0 to 16 years, male or female undergoing elective adenoidectomy or adenotonsillectomies with or without grommets insertion with one or more of the following risk factors (I-III) with the plan to use a laryngeal mask airway (as assessed by an anaesthetist independent of the study team):
  • I.Airway susceptibility as defined as 1 or more of the following
  • a.Cold or flu in the last two weeks
  • b.Wheezing > 3 times in the last 12 months
  • c.Wheezing at exercise
  • d.Nocturnal dry cough
  • II.Current or past eczema
  • III.Positive family history as defined as 1 or more of the following
  • a.=2 family members with asthma
  • b.=2 family members with eczema
  • c.=2 family members with hayfever
  • d.Only mother smoking or mother and father smoking

排除标准

  • Known cardiac disease, airway or thoracic malformations, need for premedication with midazolam.

研究者

发起方
Britta von Ungern-Sternberg

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