Feasibility and Safety of Umbilical Cord Blood Transfusion in the Treatment of Neonatal Cerebral Ischemia and Anemia
Umbilical Cord Blood Mononuclear Cell Bank in Hong Kong and Treatment of Neonatal Cerebral Ischemia and Anemia - Part IV Clinical Trial
Lead SponsorMononuclear Therapeutics Ltd.
Indication/ConditionHypoxic-Ischemic Encephalopathy Hypoxia Neonatal Cerebral Ischemia of Newborn Anemia, Neonatal
Intervention/Treatmentautologous umbilical cord blood (UCB) ...
The study is to investigate the feasibility and safety of autologous umbilical cord blood transfusion to treat the newborn infants with presence of clinical indications of neonatal hypoxic-ischemia encephalopathy (HIE) and anemia. Umbilical cord blood (UCB) is collected following labor and is transfused intravenously within 48 hours after the birth. Newborn infant without UCB available recieves the standard care will be enrolled as control group.
Following the autologous UCB transfusion in the study group or standard care in the control group, HIE subjects will be followed for 2 years for survival and neurodevelopmental outcomes and anemia subjects will be followed for 6 months to assess the survival and change of hematocrit and hemoglobin levels.
autologous UCB transfusion to the newborn infants presence of HIE and/or anemia within 48 hours after the birth
standard care procedure to the newborn infants presence of HIE and/or anemia
autologous UCB transfusion
Inclusion Criteria: evidence of asphyxiation, defined by 5-minute Apgar score ≤ 5; evidence of HIE, defined by UCB pH <7.15 or base excess ≤ 10mM; subjects with HIE confirmed by clinical features and initial investigations; subjects with evidence of anemia, defined by hematocrit < 40% or hemoglobin ≤ 13g/dL within the first 96 hours of life; obtain the informed consent from parents Exclusion Criteria: congestive cardiac failure; microcephaly, anencephaly, encephalocele, or other abnormality conjoint twins; chromosomal disorders fetal alcohol syndrome spinal bifida or other neural tube defects subjects have other neurological deficit conditions polycythemia congenital hematological malignancy investigator decision