A randomized cross-over trial in the effect of automated oxygen control devices on the distribution of oxygen saturation in preterm infants
Completed
- Conditions
- Respiratory distressventilation10028971
- Registration Number
- NL-OMON45888
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Trial ended prematurely
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 11
Inclusion Criteria
Born between 24 weeks, 0 days and 29 weeks, 6 days of gestation. Receiving invasive mechanical ventilation or non-invasive respiratory support, receiving supplemental oxygen (at least 25%), with written informed parental consent.
Exclusion Criteria
Major congenital anomalies, arterial hypotension, if attending physician considers the infant not stable enough for a switch between ventilators.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Proportion of time SpO2 spent within set target range (91-95%) </p><br>
- Secondary Outcome Measures
Name Time Method