An observational study of the gas flow delivered by bubble continuous positive airway pressure (CPAP) to preterm infants in neonatal intensive care
- Conditions
- Respiratory Distress SyndromeRespiratory - Other respiratory disorders / diseasesReproductive Health and Childbirth - Complications of newborn
- Registration Number
- ACTRN12619000197134
- Lead Sponsor
- Department of Newborn Research, The Royal Women's Hospital Melbourne
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 44
Infants born less than 37 weeks gestation.
- Currently receiving bubble CPAP therapy for any reason in the neonatal intensive care unit (NICU).
- Agreement from the treating clinician to include the infant in the study.
- Informed consent for participation in the study provided by the parent or guardian.
- Informed consent refused or withdrawn by a parent or guardian.
- Unstable clinical condition, including but not limited to respiratory distress and varying oxygen saturation.
- Deemed unsuitable by the treating clinician for participation in the study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Gas flow in litres per minute delivered by bubble CPAP at a range of set pressures to the nose of preterm infants. <br>CPAP pressure will be monitored via a pressure monitor connected to the inspiratory limb of the system. Gas flow to the infant will be read from the flow meter in L/min once bubbling has ceased in the bubble chamber.[At time of observation.]
- Secondary Outcome Measures
Name Time Method Gas flow changes in litres per minute with mouth opened or closed.<br>Gas flow to the infant will be read from the flow meter in L/min once bubbling has ceased in the bubble chamber. Mouth opening will be assessed as either open or closed by observation.[At time of observation.]