ACTRN12617001180303已完成2 期
Abdominal Functional Electrical Stimulation To Assist Ventilator Weaning In Critically Ill Patients
euroscience Research Australia0 个研究点目标入组 20 人开始时间: 2017年8月11日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 20
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. 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
- •no clearly visible separate layers of the abdominal muscles (external oblique, internal oblique and transverse abdominal muscles), assessed with ultrasound during routine care
研究者
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