This study is currently not recruiting participants.

A Phase II Multi-site Study of Autologous Cord Blood Cells for Hypoxic Ischemic Encephalopathy (HIE) - BABYBAC II

Investigating the Effects of Autologous Umbilical Cord Blood in Neonates with Hypoxic-Ischemic Encephalopathy

Not Recruiting
100 years or below
All
Phase N/A

Brief description of study.

The purpose of this study is to determine if administration of autologous umbilical cord blood will improve the outcomes of neonates with HIE who are undergoing therapeutic hypothermia.

Detailed description of study

The purpose of this study is to determine if administration of autologous umbilical cord blood will improve the outcomes of neonates with HIE who are undergoing therapeutic hypothermia.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: hypoxic ischemic encephalopathy
  • Age: 100 years or below
  • Gender: All

This study investigates the use of autologous umbilical cord blood in newborns with Hypoxic-Ischemic Encephalopathy (HIE), a condition where the brain does not receive enough oxygen and blood. The study aims to see if this treatment can improve outcomes for these newborns who are also receiving a cooling therapy called therapeutic hypothermia.

Participants in the study will receive their own umbilical cord blood. This involves collecting the blood from the umbilical cord right after birth and using it as a treatment. Therapeutic hypothermia, which is a cooling treatment, will also be administered to help protect the brain.

  • Who can participate: The study is open to newborns and infants diagnosed with Hypoxic-Ischemic Encephalopathy (HIE).
  • Study details: Participants will have their own umbilical cord blood collected and used as part of the treatment in combination with therapeutic hypothermia.
Updated on 19 Feb 2024. Study ID: 1601543756

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