Heterologous Cord Blood-Derived Red Blood Cell for Transfusion in Extremely Preterm Infants
NCT07502781
Anemia, Anemia Neonatal
Barcelona, Spain
View Trial DetailsNCT Number: NCT07296393
This single-center prospective cohort study aims to describe the distribution of umbilical-cord blood vitamin A concentrations in extremely preterm infants (<32 weeks' gestation) and to evaluate whether low cord blood vitamin A is associated with increased risk of neonatal morbidities such as bronchopulmonary dysplasia (BPD), necrotising enterocolitis (NEC), severe intraventricular haemorrhage (IVH), retinopathy of prematurity (ROP), periventricular leukomalacia (PVL), high-grade patent ductus arteriosus (hsPDA), respiratory distress syndrome (RDS), sepsis and death before discharge.
Trial opening soon.
Get NotifiedUp to 28 day
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Gestational age <32 weeks Birth at First Hospital of Jilin University Umbilical cord blood sample obtained within 24 h Parental written informed consent
Exclusion criteria
Major congenital malformation or chromosomal abnormality Refusal of consent
Time frame: From birth to 36 weeks' PMA or discharge, up to 3 months chronological age.
Contact information is provided by the study sponsor or research team.
The First Hospital of Jilin University
Other
The Association Between Umbilical Cord Blood Vitamin A Levels and Adverse Outcomes in Extremely Preterm Infants: A Single-Center Prospective Cohort Study
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