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OpenTrials
Completed

NCT Number: NCT01539356

Hepcidin Levels in Preterm Infants

A recently isolated peptide hormone, hepcidin, is thought to be the principal regulator of iron homeostasis. Hepcidin acts by limiting intestinal iron absorption and promoting iron retention in reticuloendothelial cells. The aims of this study were to determine serum hepcidin levels in preterm infants who receive blood transfusion and preterm infants having sepsis, in order to assess possible relationships between hepcidin and serum iron, serum ferritin,in iron load situations.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Preterm < 38 weeks gestation
  • Need of blood test for anemia or suspected sepsis

Exclusion criteria

  • Major congenital anomalies
  • Birth Asphyxia

Treatment and study plan

Primary outcomes

  1. Increase in Hepcidin levels by 30%

    Time frame: within 24-72 h

Sponsors and collaborators

Lead sponsor

Meir Medical Center

Other

Registry information

Official study title

Hepcidin Levels in Preterm Infants Receiving Blood Transfusion and During Sepsis.

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Feb 27, 2012
Registry last updated
Mar 16, 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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