MedPath

Multi-Center Clinical Database of Infants for the Investigation of Early Nutrition Biomarkers

Conditions
Infant Development
Registration Number
NCT05049655
Lead Sponsor
ByHeart
Brief Summary

An observational study to generate a long-term outcome database from medical records for infants who completed protocol SS-101-18 or infants who are breastfed, fed commercial formula, or fed a marketed ByHeart formula.

Detailed Description

The first Cohort (Cohort 1) goals of the registry include: to compile a clinical database of children who were fed in SS-101-18 by breastfeeding, commercial formula, or ByHeart formula; to investigate any difference in demographics, growth, development, medical diagnoses, and outcomes between the feeding groups, and in particular to compare ByHeart formula-fed infants against commercial formula-fed infants, and referenced against breastfed infants.

The second Cohort (Cohort 2) goals of the registry include: to compile a clinical database of children who were fed by breastfeeding or commercial formula (including ByHeart formula); to describe any difference in growth, development, medical diagnoses, and outcomes based on early nutritional intake; and to inform or facilitate development of future ByHeart products.

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
2000
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cohort 2: Growth, Development, Diagnoses, and Long-term Outcomes5 years

A clinical database of children of all feeding options; to describe any difference in growth, development, medical diagnoses, and outcomes based on early nutritional intake

Cohort 1: Growth, Development, Diagnoses, and Long-term Outcomes5 years

The registry will be utilized to investigate growth, development, diagnoses, and long-term outcomes of infants who received ByHeart study formula, commercially available formula, or breastmilk in the SS-101-18 protocol.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (8)

Clinical Research Prime (Cohort 1)

🇺🇸

Idaho Falls, Idaho, United States

Tanner Clinic (Cohort 1)

🇺🇸

Layton, Utah, United States

Alabama Clinical Therapeutics, LLC (Cohort 1)

🇺🇸

Birmingham, Alabama, United States

Watching Over Mothers & Babies (Cohort 1)

🇺🇸

Tucson, Arizona, United States

The Children's Clinic of Jonesboro (Cohort 1)

🇺🇸

Jonesboro, Arkansas, United States

Pediatric Associates Mt. Carmel (Cohort 1)

🇺🇸

Cincinnati, Ohio, United States

Coastal Pediatric Research (Cohort 1)

🇺🇸

Summerville, South Carolina, United States

Holston Medical Group (Cohort 1)

🇺🇸

Kingsport, Tennessee, United States

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