Soluble Urokinase Plasminogen Activator Receptor (suPAR) in Late-onset Neonatal Sepsis

NCT01294865 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2011-02-14

No results posted yet for this study

Summary

The purpose of the study is to investigate the plasma levels of Soluble Urokinase Plasminogen Activator Receptor (suPAR) at the diagnosis and after treatment of sepsis, and to determine whether it has a diagnostic and prognostic value in late-onset neonatal sepsis.

Conditions

  • Neonatal Sepsis

Sponsors & Collaborators

  • Ankara University

    lead OTHER

Principal Investigators

  • Saadet Arsan, Professor · Ankara University

Eligibility

Min Age
4 Days
Max Age
1 Month
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2012-01-31
Completion
2012-06-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01294865 on ClinicalTrials.gov