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临床试验/ACTRN12615000565549
ACTRN12615000565549已完成未知

The effect of lung volume recruitment, performed daily for three months, on maximal insufflation capacity in people with neuromuscular disease and respiratory system involvement.

Institute for Breathing and Sleep0 个研究点目标入组 80 人开始时间: 2015年6月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
80

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
14 Years 至 o limit(—)
性别
All

入选标准

  • Neuromuscular disease of >3 months duration
  • Respiratory system involvement (FVC <80% predicted)

排除标准

  • Previously prescribed daily LVR therapy which was performed for a period of >3 consecutive months in the last 12 months, or >6 consecutive weeks within the past 6 months
  • Medical instability
  • Inpatient admission for acute respiratory compromise in the preceding 6 weeks
  • Inability to provide informed consent
  • Not proficient in English
  • Requiring invasive ventilation via tracheostomy tube
  • Previous history or perceived risk factors for pneumothorax
  • Contraindication or precautions for positive pressure therapy / LVR manoeuvres

研究者

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