Trial of NCPAP Interface Leakage (ToNIL): A Randomised Crossover Comparison of Leakage With Nasal Prongs and Nasal Mask Interface in Newborn Infants Treated With CPAP
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Leakage in the CPAP system
研究概览
简要总结
The study is a two-armed randomized cross-over comparison of leakage with nasal prongs and nasal mask interface in newborn infants treated with CPAP, born after 28 weeks of gestational age. For infants with an interface leakage, the trial also includes an observational part evaluating simple measures to reduce leakage.
The study will be carried out in the Karolinska University Hospital Stockholm and in the Östersund Hospital.
详细描述
The study will recruit a total of 50 infants receiving CPAP for respiratory support at the Karolinska University Hospital and the Östersund Hospital. The infant should be stable and not in major respiratory distress. Consent from the parents will be obtained before enrolment.
The included infants should have stable spontaneous breathing and be older than 28 weeks (corrected age) at the time of enrolment. The reason for respiratory failure and CPAP treatment is not relevant for study purposes. If an infant cannot participate in the study at a given time, he or she can be enrolled later. A child can only participate once.
The primary outcome is leakage. This is recorded using equipment for measuring air flow during CPAP treatment. Measurement of leakage is first performed for one interface and then the next (cross-over). The interface order is randomized. The leakage will be measured after a few minutes of stabilization (part 1). If there is leakage, a few simple measures to reduce the leakage will be evaluated (part 2). The second part will approximately add 10-20 minutes and includes simple measures such as adjusting the nasal mask, closing the mouth, changing the position or changing the size of nasal mask/prongs. Part 1 and part 2 are then repeated for the next interface. If the child shows signs of distress or agitation the measurement will be paused or stopped.
Part 1: The CPAP system with the randomized interface (nasal mask or nasal prongs) is applied and adjusted by experienced NICU staff. The staff is blinded for the outcome variable, leakage. The choice of size and other adjustments are guided by clinical experience and not by protocol. The NICU staff is not allowed to participate in the explorative part where measures to reduce leakage are evaluated. This precaution is to avoid staff learning what adjustments affect leakage and influence care of infants enrolled at a later stage.
Part 2: In this part the investigators can evaluate the effect of simple measures to minimize the leakage. The level of leakage is displayed on a screen. Examples of measures are; closing the mouth of the infant, adjusting straps, adjusting position and changing the size of the interface. Not every child will undergo all measures to reduce leakage, since the aim of this explorative part is to explore ways to reduce leakage.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- — 至 44 Weeks(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Gestational age over 28 weeks (corrected age) at the time of inclusion
- •Patient receiving respiratory support with CPAP
排除标准
- •Airway, pulmonary, cardiac or gastro-intestinal malformations
- •Neuromuscular disease
- •Circulatory unstable patient
- •FiO2 higher than 0.5
- •Nasal damage or major skin irritation.
- •Extubation less than 24 h before investigation
- •Surgery less than 5 days before investigation
研究组 & 干预措施
Nasal mask interface
The CPAP interface will be applied and adjusted by experienced staff blinded to the outcome variable; leakage. Measures to reduce/minimize leakage are tested in an unblinded observational part after the intervention.
干预措施: Nasal mask interface (Device)
Nasal prongs interface
The CPAP interface will be applied and adjusted by experienced staff blinded to the outcome variable; leakage. Measures to reduce/minimize leakage are tested in an unblinded observational part after the intervention.
干预措施: Nasal prongs interface (Device)
结局指标
主要结局
Leakage in the CPAP system
时间窗: 0-60 min
Measurement of absolute leakage (at interface or mouth) using flowmeters connected to the CPAP device in flow through position (L/min, 30 seconds recording)
次要结局
- Level of CPAP support (cmH2O)(0-60 min)
- Peripheral oxygen saturation (SpO2)(0-60 min)
- Measurement completion possible (yes/no)(0-60 min)
- Effect of simple measures to reduce leakage (L/min)(0-60 min)
- Inspired oxygen level (FiO2)(0-60 min)
研究者
Baldvin Jonsson
Associate Professor
Karolinska Institutet
