Actively Recruiting

Phase Not Applicable
Age: 0 - 4Weeks
All Genders
NCT06266455

Individualized Nutrition to Optimize Preterm Infant Growth and Neurodevelopment

Led by Children's National Research Institute · Updated on 2025-07-11

150

Participants Needed

1

Research Sites

516 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Human milk has several well-established benefits but does not adequately meet the increased nutritional demands of the growing preterm infant, necessitating additional nutrient supplementation in a process known as fortification. In U.S. neonatal intensive care units (NICUs), human milk is primarily supplemented using standardized fortification, in which a multicomponent fortifier is added to human milk to achieve assumed nutrient content based on standard milk reference values. However, this method does not account for the significant variability in human milk composition or in preterm infant metabolism, and up to half of all very premature infants experience poor growth and malnutrition using current nutritional practices. Poor postnatal growth has adverse implications for the developing preterm brain and long-term neurodevelopment. Recent advances allow for individualized methods of human milk fortification, including adjustable and targeted fortification. Adjustable fortification uses laboratory markers of protein metabolism (BUN level) to estimate an infant's protein requirements. In targeted fortification, a milk sample is analyzed to determine its specific macronutrient and energy content, with additional macronutrient supplementation provided as needed to achieve goal values. Emerging data suggest that both methods are safe and effective for improving growth, however information on their comparable efficacy and neurodevelopmental implications are lacking, particularly using advanced quantitative brain MRI (qMRI) techniques. Through this prospective, randomized-controlled trial, the investigators will compare the impact of individualized human milk fortification on somatic growth and neurodevelopment in preterm infants. Infants will be randomized to receive one of three nutritional interventions: standardized (control group), adjustable, or targeted human milk fortification. Infants will undergo their assigned nutritional intervention until term-equivalent age or discharge home, whichever is achieved first. Brain qMRI will be performed at term-corrected age, and neurodevelopmental follow-up will be performed through 5 years of age.

CONDITIONS

Official Title

Individualized Nutrition to Optimize Preterm Infant Growth and Neurodevelopment

Who Can Participate

Age: 0 - 4Weeks
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Birth gestational age of 32 weeks or less
  • Postnatal age of 4 weeks or less at enrollment
  • Maternal plan to provide human milk and consent to donor milk if needed
  • Maternal age over 18 years
Not Eligible

You will not qualify if you...

  • Formula feeding before 36 weeks postmenstrual age or discharge home
  • Presence of congenital anomalies suggesting genetic or metabolic disorders
  • Major brain abnormalities detected by ultrasound before enrollment

AI-Screening

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Trial Site Locations

Total: 1 location

1

Children's National Hospital

Washington D.C., District of Columbia, United States, 20010

Actively Recruiting

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Research Team

C

Catherine Limperopoulos, Ph.D.

CONTACT

K

Katherine M. Ottolini, M.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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Individualized Nutrition to Optimize Preterm Infant Growth and Neurodevelopment | DecenTrialz