Actively Recruiting

Phase Not Applicable
Age: 6Hours - 4Days
All Genders
NCT06420531

Milk And Growth In Children (MAGIC) Born Very Preterm: A Randomized Trial

Led by University of Alabama at Birmingham · Updated on 2025-09-17

486

Participants Needed

4

Research Sites

258 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this multi-center randomized, parallel group trial is to determine the effect of human milk diets ranging between 180 and 200 mL/kg/day on the body composition outcomes of moderately preterm infants born between 27 and 31 weeks of gestation.

CONDITIONS

Official Title

Milk And Growth In Children (MAGIC) Born Very Preterm: A Randomized Trial

Who Can Participate

Age: 6Hours - 4Days
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Born between 27 0/7 and 31 6/7 weeks gestation
  • Birthweight of 1500 grams or less
  • Fed human milk during the first 14 days after birth
  • Reached full enteral feeding (120 mL/kg/day or more) within the first 14 days after birth
Not Eligible

You will not qualify if you...

  • Necrotizing enterocolitis stage 2 or greater
  • Spontaneous intestinal perforation
  • Major congenital or chromosomal anomalies
  • Terminal illness requiring limited or withheld support
  • Planned fluid restriction after 14 days due to symptomatic patent ductus arteriosus
  • Any formula feeding within the first 14 days after birth

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35294

Actively Recruiting

2

University of Mississippi Medical Center

Jackson, Mississippi, United States, 39216

Not Yet Recruiting

3

University of Texas Southwestern Medical Center at Dallas

Dallas, Texas, United States, 75235

Not Yet Recruiting

4

University of Texas Health Science Center at Houston

Houston, Texas, United States, 77030

Not Yet Recruiting

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Research Team

A

Ariel A. Salas, MD, MSPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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