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临床试验/ISRCTN64997093
ISRCTN64997093已完成不适用

Comparison of the laryngeal mask airway Ambu Aura Once™ and the i-gel™ in elective anaesthetised and ventilated paediatric patients

Inselspital, University Hospital Bern (Switzerland)0 个研究点目标入组 240 人开始时间: 2009年11月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
240

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Patients of both genders, aged 0-17 years
  • 2. Weight of 5-50 kg
  • 3. American Society of Anaesthesiologists (ASA) physical status I-II
  • 4. Scheduled at the University Hospital of Bern for elective surgery planned for general anaesthesia not requiring tracheal intubation

排除标准

  • 1. Planned operation time >4h
  • 2. Risk of aspiration (non-fasted, massive gastroesophageal reflux disease, gastrointestinal stenosis or stricture)
  • 3. Known difficult airway (difficult mask ventilation or difficult laryngoscopy, Cormack-Lehane grade >2)
  • 4. Congenital malformations involving the respiratory tract
  • 5. Cervical spine disease
  • 6. Upper respiratory tract symptoms in the previous 14 days
  • 7. Preoperative sore throat
  • 8. Patients with non-German-speaking parents or refusing to participate

研究者

发起方
Inselspital, University Hospital Bern (Switzerland)

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