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NOT YET RECRUITING
NCT06220461
NA

Folic Acid Supplementation to Reduce Anemia in Extremely Preterm Infants

Sponsor: University of Calgary

View on ClinicalTrials.gov

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

Interventions

DIETARY_SUPPLEMENT

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