Status:
RECRUITING
PRICO: OPTI Target Range
Lead Sponsor:
Czech Technical University in Prague
Collaborating Sponsors:
University Hospital, Motol
Conditions:
Neonatal Respiratory Distress
Very Low Birth Weight Infant
Eligibility:
All Genders
2+ years
Phase:
NA
Brief Summary
The aim of the study is to determine if a narrower SpO2 Target Range setting automated control of FiO2 (A-FiO2) is more effective than a wider SpO2 Target Range
Detailed Description
A-FiO2 systems have consistently proven to be more effective than manual control. Because it is more precise than manual control, studies of some A-FiO2 systems found small differences in the set targ...
Eligibility Criteria
Inclusion
- All VLBW on respiratory support and oxygen requirements after 2 weeks of age in the NICU are eligible after informed consent is obtained.
Exclusion
- Informed consent is not obtained
- Recording device for automated control of FiO2 is not available
Key Trial Info
Start Date :
February 20 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2025
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT06207994
Start Date
February 20 2024
End Date
September 1 2025
Last Update
March 25 2025
Active Locations (1)
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1
Motol University Hospital
Prague, Czechia, 15500