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N-Terminal Pro-brain Natriuretic Peptide Hormone and Persistent Pulmonary Hypertension

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Christiana Care Health Services

Status

Terminated

Conditions

Persistent Pulmonary Hypertension of Newborn

Study type

Observational

Funder types

Other

Identifiers

NCT00443859
CCC 27004

Details and patient eligibility

About

Babies who are suspected of having persistent pulmonary hypertension (PPHN) will be included in this study. PPHN is a condition in which the blood is restricted from flowing to the lungs in a normal way making it hard for babies to breath and placing strain on the heart. This study will observe whether certain hormones that measure stress (N-terminal pro-brain natriuretic peptide) can help determine how well a baby will do when they have PPHN.

Full description

PPHN occurs in infant > or = 34 weeks gestation and is characterized by an elevation in pulmonary vascular resistance (PVR) and right-to-left shunting of the blood at the atrial, ductal, and pulmonary levels, leading to hypoxemia. Management of these infants is complex (and the clinical course) is often difficult to predict.

Brain natriuretic peptide (BNP) is a cardiac hormone that is secreted from cardiac myocytes and cardiac fibroblasts. Upon activation, the prohormone is cleaved into a biologically active BNP and an inactive N-terminal proBNP (NT-proBNP). BNP and NT-proBNP levels are increasingly being used for diagnostic purpose in adults and have been correlated to adult pulmonary hypertension. Multiples studies have been performed to determine normal values for NT-proBNP in the pediatric population. One study measured NT-proBNP levels in umbilical cord blood during the second trimester and at delivery of uncomplicated pregnancies and determined normal reference values of NT-proBNP. It is thought that NT-proBNP has potential for use in term infants with PPHN.

The objective of this research is to correlate NT-proBNP levels to left ventricular dysfunction in term infants with PPHN. Secondarily, we want to assess the possible use of NT-proBNP to predict response to inhaled nitric oxide and the ability to successfully wean off inhaled nitric oxide.

Enrollment

10 patients

Sex

All

Ages

Under 6 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • >/= 34 weeks gestation at birth
  • clinical diagnosis of PPHN

Exclusion criteria

  • newborns with evidence of structural heart disease, congenital anomalies and prior use of inhaled nitric oxide.

Trial design

10 participants in 1 patient group

PPHN
Description:
Infants with persistent pulmonary hypertension (PPHN)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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