跳至主要内容
临床试验/NCT00969189
NCT00969189终止不适用

A Cohort Evaluation of the Pediatric Igel Airway in 200 Children and in 50 Infants

University Hospitals Bristol and Weston NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2009年8月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
120
试验地点
1
主要终点
Does the i-gel (a new supraglottic airway device) perform adequately in anaesthetised healthy children?

研究概览

简要总结

Once a child has been anaesthetised and is fully asleep, a special airway tube called a laryngeal mask is often inserted into their mouth to help with their breathing. This tube is removed just before the child wakes up.

A new type of airway tube, called an i-gel airway, has been developed for children, which is hoped will be easier to insert, safer once in position, and will be less likely to cause a sore throat after the anaesthetic than a standard laryngeal mask. The adult i-gel airway has been available for adults since 2007, and early trials have shown very encouraging results.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
— 至 16 Years(Child)
性别
All
接受健康志愿者

入选标准

  • All children weighing 5 -30kg
  • Classified by the American Society of Anesthesiology (ASA) as grade 1-2,
  • Scheduled for elective surgery under general anaesthesia, in whom a LMA or PLMA would otherwise be used for airway maintenance and in whom neuromuscular blocking drugs will not be used.

排除标准

  • Inability of patient or parents to understand the study or consent process
  • Neck pathology
  • Previous or anticipated airway problems
  • Pathology of airway, respiratory tract, upper gastrointestinal tract
  • Increased risk of regurgitation or aspiration
  • Weight >30kg or <5 kg
  • ASA 3 and above,
  • Emergency surgery

结局指标

主要结局

Does the i-gel (a new supraglottic airway device) perform adequately in anaesthetised healthy children?

时间窗: during anaesthesia

次要结局

  • Ease of insertion, Complication rates and manipulation rates during use, Airway seal pressure, Effective ventilation, Post-operative sequelae(during anaesthesia and up to 24 hours postoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Michelle White

Consultant in Paediatric Anaesthesia and Critical Care

University Hospitals Bristol and Weston NHS Foundation Trust

研究点 (1)

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