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临床试验/ACTRN12614001203640
ACTRN12614001203640已完成未知

A comparison of treatment failure rates between newborn infants randomised to either high-flow nasal cannulae or continuous positive airway pressure as primary respiratory support in Australian non-tertiary special care nurseries.

ewborn Research Centre, The Royal Women's Hospital0 个研究点目标入组 750 人开始时间: 2014年11月17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
750

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
Open (masking not used)

入排标准

年龄范围
Hours 至 24 Hours(—)
性别
All

入选标准

  • 1. Gestational age 31 weeks' or above by best obstetric estimate
  • 2. Birth weight >1200 grams
  • 3. Age <24 hours
  • 4. Admitted to the special care nursery of a participating centre
  • 5. Require non-invasive breathing support after admission to the special care nursery, or require supplemental oxygen to maintain peripheral oxygen saturation 91-95% for >1 hour

排除标准

  • 1. After admission to the SCN, the infants has already received >4 hours of CPAP
  • 2. Previous endotracheal intubation and positive pressure ventilation, or imediate need for endotracheal intubation as determined by the treating paediatrician
  • 3. Known major congenital abnormality which may impact upon the infant's condition after birth (eg. complex congenital cardiac disease, upper airway obstruction, gastrointestinal malformations)
  • 4. Any infant who is judged by their paediatrician to require transfer to a tertiary hospital for ongoing care

研究者

发起方
ewborn Research Centre, The Royal Women's Hospital

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