ACTRN12618000214235招募中未知
Abdominal Functional Electrical Stimulation to reduce respiratory complications in spinal cord injury: a randomised controlled trial
euroscience Research Australia0 个研究点目标入组 240 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
- 招募中
- 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
- 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
- •5-10 days post cervical spinal cord injury (i.e. tetraplegia)
- •post definitive spinal surgery, where indicated
- •no respiratory complications in previous 24 hours (screening out iatrogenic complications)
排除标准
- •- mechanical ventilation dependency
- •- American Spinal Injuries Association Impairment Scale D
- •- progressive neurological disease or chronic respiratory disease
- •- physical obstacles that prevent Abdominal FES (e.g. pregnancy, abdominal trauma, pacemaker)
- •- no response to Abdominal FES (e.g. lower motor neuron impairment)
研究者
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