By InvitationNot Applicable

Florida Neonatal Neurologic Network

United States1,000 participantsStarted 2011-09-09

Plain-language summary

Create a database with selected medical information on infants born with hypoxic-ischemic encephalopathy (HIE). In addition, the following samples will be collected in a bio-repository for future studies: blood, urine, and buccal samples.

Who can participate

Age range1 Day – 3 Weeks

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Gestational Age greater than or equal to 35 weeks gestation * Birth weight greater than or equal to 1.8 kg * Less than or equal to 6 hours since insult occurred * Severe hypoxic-ischemic encepholopathy (HIE) Exclusion Criteria: * Presence of lethal chromosomal abnormalities * Severe IUGR * Significant intracranial hemorrhage with a large intracranial hemorrhage (Grade III or intraparenchymal echodensity (Grade IV))

What they're measuring

Measurement of blood-based biomarkers of neonatal Hypoxic Ischemic Encephalopathy (HIE)

Timeframe: 2 years

Trial details

NCT IDNCT02260271

SponsorUniversity of Florida

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2045-12

View on ClinicalTrials.gov More Hypoxic-Ischemic Encephalopathy trials