About this trial
Despite advances in neonatal care, moderate-to-severe acute perinatal HIE in late preterm and term infants remains a cause of mortality, neurological injury, and long-term neurodevelopmental disability. The current standard of care includes therapeutic hypothermia for 72 hours, but 40-50% of infants will die or suffer significant neurodevelopmental impairment. It has been shown that administration of hydrogen gas (H2) significantly diminishes ischemic injury in swine, and that H2 administration at the dose and duration proposed herein is well-tolerated in healthy adults. The purpose of this project is to test the feasibility and safety of H2 administration as an adjunct to therapeutic hypothermia in infants with HIE. Under exemption from informed consent, infants with severe, acute brain injury at birth will be randomized to standard therapy with or without the administration of 2% hydrogen in gases administered via the ventilator, non-invasive ventilation, or nasal cannula for 72 hours.
Eligibility criteria
Qualifiers
Infants born ≥36 weeks gestation.
sentinel event prior to delivery, such as uterine rupture, profound fetal bradycardia, or cord prolapse
low Apgar scores (≤ 5 at 10 minutes of life)
prolonged resuscitation at birth (chest compressions and/or intubation and/or mask ventilation at 10 minutes)
Disqualifiers
Enrollment in the opt-out program.
Presence of known cyanotic congenital heart disease.
Presence of known or suspected genetic/chromosomal syndrome or multiple congenital anomalies.
Presence of known congenital malformation that is expected to require urgent surgical intervention in the neonatal period, including congenital diaphragmatic hernia (CDH), gastroschisis, omphalocele, intestinal atresia, or imperforate anus.
Trial design
Treatments tested in this trial
- Hydrogen Gas (H2)