Transcutaneous bilirubin measurement: The comparison of the reliability of transcutaneous bilirubin measurement in comparison to a measurement of plasma.
Recruiting
- Conditions
- neonaten die icterisch zien en geprikt worden op hyperbilirubinemie. icteric neonates who will be pinned on hyperbilirubinaemia.
- Registration Number
- NL-OMON20391
- Lead Sponsor
- Judith DemmersOmloop 684614 ER, Bergen op ZoomThe Netherlandsjdemmers@amphia.nl076-5951575 / 076-5951591 / 06-14683021
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Neonates between 32-42 weeks gestation in which we want to determine a bilirubin.
Exclusion Criteria
1. Neonates < 32 weeks of gestation;
2. Neonates with blood type antagonism;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bilirubine levels of the two transcutaneous devices en the measurement from the serum.
- Secondary Outcome Measures
Name Time Method Comparing of the bilirubine levels from the different devices and their sensitivity en specificity.