About this trial
Hypoxic-ischemic encephalopathy (HIE) is a serious condition in newborns caused by lack of oxygen and blood flow around the time of birth. Standard treatment with cooling therapy (therapeutic hypothermia) lowers the risk of death or disability, but many infants still suffer long-term problems.
This study will test whether adding stem cell therapy after cooling can further improve outcomes. The stem cells are taken from donated human placentas (Wharton's jelly-derived mesenchymal stem cells, MSCs). The cells are prepared under strict laboratory standards and checked for safety.
Infants with moderate to severe HIE who have completed cooling will be randomly assigned to receive either three intravenous infusions of MSCs or placebo within the first 10 days of life. Each infusion is given over about 30 minutes while the infant is closely monitored.
Researchers will follow participants for up to 2 years. The main outcome is whether MSC treatment can reduce the combined risk of death or serious developmental delay at 1 year of age. The study will also track brain MRI findings, safety events, and developmental progress at 2 years.
Eligibility criteria
Qualifiers
Term and late-preterm infants (gestational age ≥34 weeks)
Diagnosed with moderate to severe HIE based on modified Sarnat staging
Received TH per standard protocol
Parental consent obtained
Disqualifiers
Major congenital anomalies or genetic syndromes
Severe sepsis or active infection
Severe coagulopathy or bleeding disorders
Multi-organ failure
Trial design
Treatments tested in this trial
- Wharton's jelly-derived mesenchymal stem cells
- 0.9 % Normal Saline
Treatment groups
Sponsors and collaborators
Mahidol University
Lead sponsor
Siriraj Hospital
Collaborator