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Folic Acid Supplementation to Reduce Anemia in Extremely Preterm Infants
Sponsor: University of Calgary
Summary
Anemia of Prematurity (AOP) is very common in extremely preterm infants and often leads to blood transfusions. Folic acid, essential for growth and DNA synthesis, is deficient in premature infants. Despite the adoption of folic acid supplementation, evidence supporting its effectiveness in preventing AOP remains scarce. Recommendations for folic acid intake exceed what's naturally found in breast milk, particularly for extremely low birthweight infants. Practices regarding folic acid supplementation vary widely, prompting the need for research. The FACINATE trial aims to determine if additional folic acid supplementation improves hemoglobin levels and reduces late blood transfusions in extremely preterm infants, a question not addressed in current literature.
Official title: Folic Acid Supplementation to Reduce the Severity of Anemia and Blood Transfusions in Extremely Preterm Infants
Key Details
Gender
All
Age Range
Any - Any
Study Type
INTERVENTIONAL
Enrollment
90
Start Date
2024-06-01
Completion Date
2028-07-31
Last Updated
2024-05-09
Healthy Volunteers
No
Conditions
Interventions
Folic acid
Infants allocated to the intervention group will receive folic acid (50 mcg flat dose/day) starting at 14 days of age.
Locations (1)
Foothills Medical Centre
Calgary, Alberta, Canada