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OpenTrials
Completed

NCT Number: NCT01644981

Prospective Study on Plasma Pro-endothelin-1 in Predicting Bronchopulmonary Dysplasia

Serial quantitative measurements of plasma pro-endothelin-1 concentrations in very preterm infants. Comparing pro-endothelin-1 with established clinical indices of bronchopulmonary dysplasia (BPD). Hypothesis: Pulmonary-vascular remodeling in infants developing BPD is directly related to circulating pro-endothelin-1, which therefore serves as surrogate marker of BPD.

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Key information

Age range

2 week–4 month

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Zurich, Division of Neonatology

Zurich, Canton of Zurich, 8091, Switzerland

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Very preterm infants born before 32 weeks gestational age

Exclusion criteria

  • Severe fetal malformation, congenital heart defect, inborn syndrome, cardiomyopathy, fetal hydrops

Treatment and study plan

Blood sampling

Other

blood sampling

Primary outcomes

  1. duration of supplemental oxygen requirement

    Time frame: 36 weeks postmenstrual age

    Bronchopulmonary dysplasia

Secondary outcomes

  1. duration of respiratory pressure support

    Time frame: during hospitalisation

    respiratory pressure support either mechanical and/or nCPAP (days)

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Collaborators

  • University Children's Hospital Basel

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jul 19, 2012
Registry last updated
May 10, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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