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Cerebrospinal fluid metabolites as marker for the severity of progressive post-hemorrhagic ventricular dilatation in preterm infants

Cerebrospinal fluid metabolites as marker for the severity of progressive post-hemorrhagic ventricular dilatation in preterm infants - Cerebrospinal fluid metabolites in post-hemorrhagic ventricular dilatation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30135
Enrollment
125
Registered
2006-08-24
Start date
2006-09-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

hydrocephalus after cerebral bleeding

Interventions

None listed

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: Preterm infants (gestational age

Exclusion criteria

Exclusion criteria: congenital cerebral malformation cerebral parenchymal hemorrhage/infarction periventricular leucomalacia PHVD already present at birth infection of the CNS metabolic disorder

Design outcomes

Primary

MeasureTime frame
The concentration of brain specific proteins and glucose in CSF, the severity of ventricular dilatation, VP drain insertion and neurodevelopmental outcome at the age of 2 year.

Secondary

MeasureTime frame
None.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)