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临床试验/ACTRN12610000075088
ACTRN12610000075088已完成未知

'A randomised controlled trial of tracheostomy patients in intensive care receiving early versus standard Speech Pathology intervention, does this lead to improved time to verbal communication and patient reported quality of life/satisfaction?'

Royal Prince Alfred Hosptial0 个研究点目标入组 30 人开始时间: 2010年1月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
30

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

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Air filled cuffed tracheostomy tube
  • Mechanically ventilated with Postive end expiratory pressure (PEEP) Tracheostomy formed for minimum 48 hours
  • Spontaneously triggering ventilator
  • Able to obey commands
  • Clincally stable (respiratory rate between 8-24 breaths per minute, oxygen saturation >88% of peripheral oxygen saturation(SpO2), heart rate between 40-120 beats/min and systolic blood pressure between 90-160mmHg)

排除标准

  • Contra indication to cuff deflation as per treating intensivist (eg bulbar palsy, brainstem cerebral vascular accident (CVA)
  • Recent Head and neck surgery

研究者

发起方
Royal Prince Alfred Hosptial

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