跳至主要内容
临床试验/NCT01588080
NCT01588080已完成不适用

A Pilot Study Comparing Infant Flow SiPAP to Noninvasive NAVA

Fraser Health3 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2012年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
21
试验地点
3
主要终点
total duration of respiratory support which includes both days and hours on NAVA/SiPAP (DORS)

研究概览

简要总结

When babies are born premature, they often need help with their breathing. The equipment used to help them breathe is not very comfortable and they sometimes need to be put on a specialized breathing machine with a tube into their lungs. The breathing machine or ventilator can be damaging to the newborn's lungs and more damage can occur the longer the newborn stays on a ventilator leading to chronic lung disease later in their lives. A new device called neurally adjusted ventilatory assist or NAVA is available that the investigators believe may be more comfortable for the premature newborn and may help the baby come off breathing support sooner. When using this device, babies may not need to be put on a ventilator and can avoid the lung damage associated with the breathing tube and the ventilator. The objective of this pilot study is to compare this new breathing device called NAVA, to the equipment that is currently being used, called SiPAP, to support premature newborn's breathing after birth without a breathing tube. The investigators hope to show that with this new technology, premature newborns that are having a difficult time breathing, will come off breathing support sooner compared to the breathing machines that are currently being used. The hypothesis for this proposed study is that improved synchrony with noninvasive NAVA will decrease time spent on noninvasive ventilation and avoid intubation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
28 Weeks 至 32 Weeks(Child)
性别
All
接受健康志愿者

入选标准

  • Infants born greater than or equal to 28+0 weeks and less than or equal to 31+6 weeks gestation
  • Diagnosis of RDS in the first 24 hours of life requiring respiratory support
  • Parental consent obtained

排除标准

  • Infants with a major congenital anomaly
  • Infants with pulmonary hypoplasia
  • Infants known or suspected to have a neuromuscular disorder
  • Infants less than 28+0 weeks GA
  • Intubated infants that are likely to require continued mechanical ventilation
  • Infants requiring vigorous resuscitation at birth, including chest compressions +/- cardiac medications

结局指标

主要结局

total duration of respiratory support which includes both days and hours on NAVA/SiPAP (DORS)

时间窗: one year

次要结局

  • All cause mortality during the hospitalization(one year)
  • Total duration of oxygen requirement(one year)
  • Proportion of infants that required escalation to increased noninvasive respiratory support (BiPhasic or increasing NAVA levels) or intubation and mechanical ventilation(one year)
  • Number of doses of surfactant(one year)
  • Time to reach full volume feeds (at least 120 ml/kg/day)(one year)
  • Time to regain birth weight(one year)
  • Bronchopulmonary dysplasia defined as oxygen requirements or ventilatory support needs at 36 weeks CGA(one year)
  • Incidence of pneumothorax(one year)
  • Incidence of nasal deformities, specifically nasal erosions(one year)
  • Total length of hospital stay(one year)

研究者

发起方
Fraser Health
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ravinder Kajla

Respiratory Therapist, Clinical Resource Therapist

Fraser Health

研究点 (3)

Loading locations...

相似试验

Comparison Between Infant Flow SiPAP and Noninvasive... | 临床试验