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Plasma B-Type Natriuretic Peptide Concentrations in Preterm Infants < 28 Weeks

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00528736
Enrollment
82
Registered
2007-09-12
Start date
2005-08-31
Completion date
2007-04-30
Last updated
2007-09-14

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

Conditions

Ductus Arteriosus, Patent, Infant, Premature, Natriuretic Peptide Brain

Keywords

preterm infants < 28 weeks, B-type natriuretic peptide, prediction, ductus intervention

Brief summary

The aim of the study was to evaluate BNP in preterm infants \< 28 weeks on the second day of life, when it is still unknown, if a patent ductus arteriosus is hemodynamic significant or not. We hypothesized that high plasma BNP concentrations on day 2 are associated with the need of PDA intervention in the further course.

Detailed description

From the study infants blood samples (0.1ml) were collected in K-EDTA microtubes within 24 to 48 hours of age through umbilical artery catheter aspiration or routine venous puncture. The samples were spun at 7000 rpm for 3 minutes. Platelet-free plasma was stored at -20°C until BNP analysis of all collected samples was carried out. The BNP assay was performed using a fully automated immunoassay system ADVIA method for the Centaur System (Bayer Diagnostic Division). In preterm infants who were treated with indomethacin or surgical ligation we collected additional blood samples 2-4 hours before intervention and 24 hours after the completion of the ductus treatment.

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
24 Hours to 48 Hours
Healthy volunteers
No

Inclusion criteria

* Written parental informed consent * Preterm infant \< 28 weeks of gestation * Admitted to our NICU within 48 hours after birth

Exclusion criteria

* No written parental informed consent, * Congenital heart disease, * Death

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026