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临床试验/ACTRN12618000209291
ACTRN12618000209291尚未招募未知

Abdominal Functional Electrical Stimulation To Assist Ventilator Weaning In Critically Ill Patients: a randomised controlled trial

euroscience Research Australia0 个研究点目标入组 254 人开始时间: 2018年2月9日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
254

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
18 Years 至 o limit(—)
性别
All

入选标准

  • mechanical ventilation dependence due to critical illness

排除标准

  • expected to be ventilated for < 24 hours (based on clinical judgement)
  • ventilated for > 72 hours (to avoid excessive muscle atrophy)
  • non-pharmacological paralysis (e.g. spinal cord injury or Guillain-Barré syndrome)
  • physical obstacles that prevent Abdominal FES (e.g. pregnancy, severe abdominal trauma, pacemaker)
  • terminal illness
  • no response to Abdominal FES (e.g. lower motor neuron impairment)
  • recent abdominal surgery within four weeks prior to study inclusion

研究者

发起方
euroscience Research Australia

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