Prolonged automatic oxygen support in preterm infants
- Conditions
- hypoxemia, hyperoxemia, hypoxie, hyperoxie
- Registration Number
- NL-OMON27305
- Lead Sponsor
- Academic Medical Center (AMC), Amsterdam
- Brief Summary
one
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Preterm infants will be enrolled based on the following inclusion criteria:
• From day 7 of life after being born with a gestational age under 28 weeks
Exclusion Criteria
• Major congenital anomalies
• If the attending physician deems participation in the study is not in the best interest of the infant
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The hypotheses of this trial are based on the need to assess the effectiveness of A-FiO2 adjustments over time. The primary outcome variable is therefore defined as the proportion of time for both control settings with SpO2 within the assigned saturation TR (87-95%), measured over a time period of maximum 28 days and excluding time with SpO2 above the range while FiO2 is set at 0.21.
- Secondary Outcome Measures
Name Time Method