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Procalcitonin as parameter for neonatal infection

Procalcitonin as parameter for neonatal infection - Pro-EOS study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49787
Enrollment
180
Registered
2019-03-28
Start date
2019-04-22
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

infection of the newborn Perinatal infection

Interventions

None listed

Sponsors

Spaarne Gasthuis
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: • Amenorrhea of >= 32 weeks, age

Exclusion criteria

Exclusion criteria: • (Suspected) chromosomal abnormalities or severe congenital anomalies. • Neonates born in an other hospital/neonates who have been admitted to another hospital in the past.

Design outcomes

Primary

MeasureTime frame
The sensitivity and specificity of PCT for infection in the newborn tested in the umbilical cord blood, and in subsequent follow-up measurements in venous blood.

Secondary

MeasureTime frame
- The level of PCT measured in umbilical cord blood. - The level of PCT and CRP in the blood measured in newborns with a (suspected) infection.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)