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Growth and Tolerance of Young Infants Fed Infant Formula

Not Applicable
Completed
Conditions
Growth and Tolerance
Interventions
Other: Experimental Infant Formula
Other: Control Infant Formula
Registration Number
NCT04105686
Lead Sponsor
Abbott Nutrition
Brief Summary

This is a randomized, multicenter, controlled, double-blind, parallel study to evaluate growth and tolerance of healthy term infants fed milk-based infant formulas.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
366
Inclusion Criteria
  • Participant is judged to be in good health as determined from participant's medical history.
  • Participant is a singleton from a full-term birth with a gestational age of 37-42 weeks.
  • Participant's birth weight was > 2490 g (~5 lbs. 8 oz.).
  • Parent(s) who elect to formula-feed the participant, confirm their intention to feed their infant the study product as the sole source of feeding during the study.
  • Parent(s) who elect to feed the participant human milk, confirm their intention to exclusively feed human milk as the sole source of feeding during the study.
  • Parent(s) of formula-fed infants confirm their intention not to administer vitamin or mineral supplements, (except for vitamin D supplements), solid foods or juices to their infant from enrollment through the duration of the study.
  • Parent(s) of human milk-fed infants confirm their intention not to administer solid foods or juices to their infant from enrollment through the duration of the study (vitamins and minerals are acceptable).
  • Participant's parent(s) has voluntarily signed and dated an ICF, approved by an IRB/IEC and provided HIPAA (or applicable privacy regulation) authorization prior to any participation in the study.
Exclusion Criteria
  • An adverse maternal, fetal or participant medical history that is thought by the investigator to have potential for effects on tolerance, growth, and/or development.
  • Participant is taking and plans to continue taking medications (including over the counter), prebiotics, probiotics, home remedies, herbal preparations or rehydration fluids that might affect GI tolerance.
  • Participant participates in another study that has not been approved as a concomitant study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental Infant FormulaExperimental Infant FormulaMilk-based study product with oligosaccharides
Control Infant FormulaControl Infant FormulaMilk-based study product
Primary Outcome Measures
NameTimeMethod
WeightDay of life 14 to Day of life 119

Weight gain per day

Secondary Outcome Measures
NameTimeMethod
Stool CharacteristicsStudy Day 1 to Day of life 119

Parent completed diary

Head Circumference (HC)Day of life 14 to Day of life 119

HC gain per day

LengthDay of life 14 to Day of life 119

Length gain per day

Formula ToleranceStudy Day 1 to Day of life 119

Parent completed diary

Trial Locations

Locations (32)

Springs Medical Research

🇺🇸

Owensboro, Kentucky, United States

Central Research Associates

🇺🇸

Birmingham, Alabama, United States

Visions Clinical Research

🇺🇸

Tucson, Arizona, United States

Children's Research, LLC

🇺🇸

Lake Mary, Florida, United States

Tekton Research

🇺🇸

Chamblee, Georgia, United States

Meridian Clinical Research 3080

🇺🇸

Baton Rouge, Louisiana, United States

University Clinical Research-Deland, LLC dba Avail Clinical Research- West Volusia Pediatrics

🇺🇸

DeLand, Florida, United States

PAS Research, LLC

🇺🇸

Tampa, Florida, United States

New Horizon Research Center

🇺🇸

Miami, Florida, United States

Asclepes Research Centers

🇺🇸

Spring Hill, Florida, United States

Saltzer Health

🇺🇸

Nampa, Idaho, United States

Midsouth Center for Clinical Research

🇺🇸

Memphis, Tennessee, United States

Medical Research Center of Memphis

🇺🇸

Memphis, Tennessee, United States

ClinOhio Research Services

🇺🇸

Columbus, Ohio, United States

PriMed Clinical Research

🇺🇸

Dayton, Ohio, United States

Gadolin Research, LLC

🇺🇸

Beaumont, Texas, United States

Ohio Pediatric Research Association

🇺🇸

Dayton, Ohio, United States

Score Physician Alliance, LLC

🇺🇸

Saint Petersburg, Florida, United States

TOPAZ Clinical Research, Inc.

🇺🇸

Apopka, Florida, United States

Wake Research - Clinical Research Center of Nevada

🇺🇸

Las Vegas, Nevada, United States

Aspen Clinical Research LLC

🇺🇸

Orem, Utah, United States

Southeastern Pediatric Associates

🇺🇸

Dothan, Alabama, United States

Applied Research Center of Arkansas

🇺🇸

Little Rock, Arkansas, United States

Deaconess Clinic, Inc.

🇺🇸

Evansville, Indiana, United States

Meridan Clinical Research

🇺🇸

Omaha, Nebraska, United States

Mercury Clincial Research, Inc.

🇺🇸

Houston, Texas, United States

Institute of Clinical Research, LLC

🇺🇸

Mentor, Ohio, United States

Women's Hospital at Renaissance - Doctors Hospital at Renaissance

🇺🇸

Edinburg, Texas, United States

MultiCare Institute for Research and Innovation

🇺🇸

Tacoma, Washington, United States

Pediatric & Adult Research Center

🇺🇸

Orlando, Florida, United States

The Cleveland Pediatric Research Center, LLC

🇺🇸

Middleburg Heights, Ohio, United States

DCOL Center for Clinical Research

🇺🇸

Longview, Texas, United States

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