Determination of SpO2 differencesbetween different SpO2 sensors, approved for monitoring of premature and newborn infants
- Conditions
- Clinical monitoring (SpO2)
- Registration Number
- DRKS00027285
- Lead Sponsor
- niversitätsklinikum Tübingen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
Premature infants <32 weeks of gestation (of which at least 9 premature infants <28 weeks gestation and at least 9 premature infants with FiO2 requirement >0.21 (combinations possible))
- Echocardiographically excluded open ductus arteriosus botalli with bi-directional or right-left shunt.
Exclusion Criteria
- Palliative care situation
- Less than 12 meals a day
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Average percentage deviation of the determined SpO2 values ??between LNCS sensors and PPG or RD sensors
- Secondary Outcome Measures
Name Time Method - Mean deviation in the SpO2 ranges <80%, 80-89%, 90-95% and> 95%.<br><br>-% time in target (SpO2 90-95%),% time above target,% time below target,<br><br>-% time with hypoxemia (SpO2 <80%),% time with hyperoxemia (SpO2> 97%)<br>