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Protein Supplement
Protein-Enriched Human Milk for Premature Infants
N/A
Waitlist Available
Led By Ariel Salas, MD, MSPH
Research Sponsored by University of Alabama at Birmingham
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Postnatal age < 96 hours
Be younger than 18 years old
Must not have
Chromosomal anomalies
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years of corrected age
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether giving extremely preterm infants milk with extra protein helps them grow stronger and develop healthier guts compared to regular milk. Some infants will receive milk with extra protein shortly after birth, while others will receive regular milk. Researchers hope to see better growth and gut health in the babies who get the extra protein. Protein supplementation of human milk has been studied to improve growth and development in preterm infants, but results have been mixed.
Who is the study for?
This trial is for extremely preterm infants born at or before 28 weeks of gestation and are less than 96 hours old. It's not suitable for babies with chromosomal anomalies, significant congenital malformations, or those with a terminal illness where medical support would be limited.
What is being tested?
The study is testing if feeding extremely preterm infants a protein-enriched human milk diet versus the usual human milk diet can improve their growth without fat gain and help develop their gut bacteria by the time they reach their due date.
What are the potential side effects?
Since this trial involves dietary changes in very young infants, potential side effects may include digestive issues such as intolerance to the enriched formula, which could affect how well they feed and grow.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My baby is less than 4 days old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My condition involves chromosomal anomalies.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years of corrected age
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years of corrected age
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Fat-free Mass(FFM)-For-age Z-score
Secondary study objectives
Anthropometric Measurements
Body Fat(BF)-For-age Z-score
Culture-proven Sepsis
+10 moreOther study objectives
Changes in Intestinal Microbiome
Cognitive Outcomes
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Protein-enriched human milk dietExperimental Treatment1 Intervention
Infants in this group will receive protein-enriched expressed human milk or donor human milk during the first 2 weeks after birth.
Group II: Usual human milk dietActive Control1 Intervention
Infants in this group will receive either expressed human milk or donor human milk during the first 2 weeks after birth.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Protein-enriched human milk diets provide additional protein to support the growth and development of preterm infants. This increased protein intake promotes fat-free mass (FFM) and aids in the maturation of the gut microbiome.
These mechanisms are crucial for preterm infants, who have higher nutritional needs and immature digestive systems, making them more susceptible to growth delays and gastrointestinal issues. By enhancing protein intake, these diets aim to improve overall growth outcomes and support the development of a healthy gut microbiome, essential for nutrient absorption and immune function.
15N-tracer studies in formula-fed preterm infants: the role of glycine supply in protein turnover.Clinical evaluation of two different protein content formulas fed to full-term healthy infants: a randomized controlled trial.Higher versus lower protein intake in formula-fed low birth weight infants.
15N-tracer studies in formula-fed preterm infants: the role of glycine supply in protein turnover.Clinical evaluation of two different protein content formulas fed to full-term healthy infants: a randomized controlled trial.Higher versus lower protein intake in formula-fed low birth weight infants.
Find a Location
Who is running the clinical trial?
University of Alabama at BirminghamLead Sponsor
1,641 Previous Clinical Trials
2,331,999 Total Patients Enrolled
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,047 Previous Clinical Trials
2,730,907 Total Patients Enrolled
Ariel Salas, MD, MSPHPrincipal InvestigatorUniversity of Alabama at Birmingham
1 Previous Clinical Trials
102 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My baby is less than 4 days old.My condition involves chromosomal anomalies.
Research Study Groups:
This trial has the following groups:- Group 1: Protein-enriched human milk diet
- Group 2: Usual human milk diet
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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