A randomized controlled trial of respiratory function monitoring during stabilization of preterm infants at birth
Completed
- Conditions
- respiratory distress syndrome in preterm infants at birth10028971
- Registration Number
- NL-OMON37164
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Infants born will be included in this study if they are between 24 and 27 completed weeks
gestation receiving PPV for resuscitation at birth
Exclusion Criteria
if they are found to have a congenital abnormality
or condition that might have an adverse effect on breathing or ventilation, including: congenital
diaphragmatic hernia, tracheo-oesophageal fistula or cyanotic heart disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The proportion of tidal volumes delivered during manual PPV to an infant within<br /><br>the target range of safe tidal ventilation. The target range of adequate tidal<br /><br>volume is defined as 4-8 mL/kg. </p><br>
- Secondary Outcome Measures
Name Time Method