Open Lung Strategy During Non-Invasive Respiratory Support of Very Preterm Infants in the Delivery Room (OpenCPAP-DR)
Respiratory Distress Syndrome in Premature Infant, Non-invasive Ventilation, Lung Injury
About this trial
This is an interventional treatment trial for Respiratory Distress Syndrome in Premature Infant focused on measuring nasal CPAP, delivery room, open lung strategy, PEEP, Respiratory Distress Syndrome, Individualised ventilation
Eligibility Criteria
Inclusion Criteria:
- Infants born before 30 completed weeks of gestation and received early nCPAP immediately after birth in delivery room
Exclusion Criteria:
- Requirement of surfactant or endotracheal intubation or positive pressure ventilation before the completion of interventions
- Major congenital anomaly
- Transportation to another hospital
Sites / Locations
- Etlik Zubeyde Hanım Maternity and Children Hospital
- Dokuz Eylul University
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
openCPAP
standardCPAP
Immediately after birth, early nCPAP will be started with a nasal mask with a T-piece resuscitator with 8 cm H2O pressure and 0.30 fiO2. The heart rate (HR) and preductal saturation (SpO2) will be evaluated every 30 seconds. Individually, the following steps will be done according to the situation: If the HR > 120 / min and SpO2 not measured yet or be in the target range: The pressure will be continue as 8 cmH2O. If the HR between 100-120 but SpO2 below the target range or not measured yet : First the pressure will be increased to 10 cm H2O; than fiO2 will be increased gradually if the patient will not respond to 10 cmH2O pressure. Pressure will be reduced to 8 cmH2O if the HR remains> 120 / min and oxygen requirement <0.30 for more than 60 seconds.
Immediately after birth, early nCPAP will be started with a nasal mask with T-piece resuscitator at 6 cmH2O pressure and 0.30 fiO2. HR and preductal saturation will be evaluated every 30 seconds. The following steps will be performed according to the situation: If the HR > 120 / min and SpO2 be in the target range or not measurable yet: The pressure will be continue as 6 cmH2O. If the HR between 100-120 but SpO2 below the target range or not measured yet : The pressure will increased up to 8 cm H2O. FiO2 will be increased gradually if the patient will not respond to 8 cmH2O pressure. Pressure will be reduced to 6 cmH2O if the HR remains> 120 / min and oxygen requirement <0.30 for more than 60 seconds.