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临床试验/NCT05987800
NCT05987800已完成不适用

Non-invasive Ventilation in Preterm Infants

Universitair Ziekenhuis Brussel2 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2023年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
136
试验地点
2
主要终点
Total duration of respiratory support

研究概览

简要总结

This is a prospective, observational cohort study. For the study part on noninvasive neurally adjusted ventilatory assist (NIV-NAVA) the design is interventional. For all participants prospective data collection will be conducted by chart review and by downloading ventilatory data from the ventilator. A registration of respiratory severity score will be done by a caregiver during the weaning period. This consists of a visual assessment of the work of breathing every 2 hours. For participants on NIV-NAVA consenting to the interventional part of the study a titration procedure will be conducted, afterwards serial electrical impedance tomography and lung and diaphragm ultrasound measurements will be done.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Preterm infants (< 37 weeks GA) supported with non-invasive respiratory support for at least 24 hours. Non-invasive respiratory support can consist of non-invasive NAVA, nasal continuous positive airway pressure (nCPAP) or high flow nasal canula (flow > 2 liters/min).The support can be given as primary respiratory support or as respiratory support after weaning from invasive ventilation (= after extubation).
  • Infants can only be enrolled after written and signed informed consent by the parents.

排除标准

  • Infant born after a gestational age of 37 weeks or more.
  • Infants with major congenital malformations or chromosomal abnormalities (eg trisomy 18, congenital diaphragmatic hernia…)

研究组 & 干预措施

Preterm infants on non-invasive respiratory support

Other

All infants on non-invasive respiratory support will be studied. Only infants on less than 32 weeks of gestation at birth, will undergo an intervention.

干预措施: Titration procedure (Diagnostic Test)

Preterm infants on non-invasive respiratory support

Other

All infants on non-invasive respiratory support will be studied. Only infants on less than 32 weeks of gestation at birth, will undergo an intervention.

干预措施: Electrical impedance tomography (Diagnostic Test)

Preterm infants on non-invasive respiratory support

Other

All infants on non-invasive respiratory support will be studied. Only infants on less than 32 weeks of gestation at birth, will undergo an intervention.

干预措施: Lung and diaphragm ultrasound (Diagnostic Test)

结局指标

主要结局

Total duration of respiratory support

时间窗: From birth until study completion, variating between 3 weeks and 3 months

Total number of days of invasive and non-invasive respiratory support

Rate of bronchopulmonary dysplasia (BPD) or death

时间窗: From birth until gestational age of 36 weeks

Percentage of infants with BPD or death

次要结局

  • Duration of non-invasive respiratory support (days)(From birth until study completion, between 3 weeks and 3 months)
  • Respiratory severity score (RSS)(From start of the weaning phase until respiratory support is stopped, up to 10 weeks)
  • Description of mode of non-invasive respiratory support(From birth until study completion, between 3 weeks and 3 months)
  • Duration of invasive respiratory support (days)(From birth until study completion, variating between 3 weeks and 3 months)
  • Lung ultrasound score(At inclusion, day 3, day 7 and weekly thereafter as long as supported with NIV-NAVA, up to 10 weeks)
  • Use of surfactant and mode of administration(From birth until study completion, between 3 weeks and 3 months)
  • Use of corticosteroids for the prevention or treatment of BPD(From birth until study completion, between 3 weeks and 3 months)
  • Length of hospital stay(From birth until study completion, between 3 weeks and 3 months)
  • Incidence of nosocomial infection(From birth until study completion, between 3 weeks and 3 months)
  • NIV-NAVA breakpoint(At inclusion (within 24 hours))
  • Diaphragm ultrasound(At inclusion, day 3, day 7 and weekly thereafter as long as supported with NIV-NAVA, up to 10 weeks)
  • Silent Spaces(At inclusion, day 3, day 7 and weekly thereafter as long as supported with NIV-NAVA as long as supported with NIV-NAVA, up to 10 weeks)
  • Tidal volume (TV)(At inclusion, day 3, day 7 and weekly thereafter as long as supported with NIV-NAVA as long as supported with NIV-NAVA, up to 10 weeks)
  • Center of Ventilation (CoV)(At inclusion, day 3, day 7 and weekly thereafter as long as supported with NIV-NAVA as long as supported with NIV-NAVA, up to 10 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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