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Study identifier: NCT05170633 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Blood Warming in Preterm Infants to Decrease Hypothermia

Condition: Preterm Birth · Blood Transfusion Complication · Hypothermia  ·  Sponsor: University of South Carolina

PhaseNA
Planned participants140
Who can joinAll sexes, 24 Weeks to 32 Weeks
Healthy volunteersYes

About this study

Background/significance: Over 100,000 early preterm infants are born annually in the United States and suffer morbidity and mortality during hospitalization in a neonatal intensive care unit. One such condition is hypothermia. Hypothermia has been defined as a contributor of neonatal morbidity by The World Health Organization. Another acute morbidity is anemia in preterm infants due to the prematurity and frequent laboratory testing. Anemia requires correction with a packed red blood cells (PRBC) transfusion. Researchers have previous noted hypothermia during PRBC transfusions in preterm infants. Objective: To use a commercial blood warmer in the neonatal intensive care setting to prevent hypothermic body temperatures (\<36.5°C) in very preterm infants during PRBC transfusions. Process: Based on a completed national survey of neonatal intensive care nurses and PRBC transfusion practices and personal NICU experience, we designed this randomized control trial in 140 very preterm infants in a Southeastern, level III neonatal intensive care unit. Outcomes: Very preterm infants (\<32 weeks gestational age) receiving PRBC transfusions warmed by the commercial blood warmer will have a lower incidence of central body hypothermia post transfusion (temperatures \<36.5C), compared to infants receiving PRBC transfusions by standard of care. Very preterm infants (\<32 weeks gestational age) receiving PRBC transfusions warmed by the commercial blood warmer will have a higher post transf…

This description comes directly from the study's public registry record.

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Locations (1)

Kayla EverhartColumbia, South Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05170633