The Effects on Growth and Tolerance of a Routine Infant Formula Fed to Term Infants
1 other identifier
interventional
315
1 country
22
Brief Summary
This clinical trial will evaluate an investigational infant formula with an alternate source of DHA to determine if it provides normal growth and if it is well tolerated by term infants as compared to a marketed routine infant formula.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2014
22 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2014
CompletedFirst Submitted
Initial submission to the registry
May 5, 2014
CompletedFirst Posted
Study publicly available on registry
May 7, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2015
CompletedMay 1, 2015
April 1, 2015
10 months
May 5, 2014
April 30, 2015
Conditions
Outcome Measures
Primary Outcomes (1)
Body weight measured at each study visit
3.5 Months
Secondary Outcomes (7)
Recall of infant formula intake at each study visit
3.5 months
Body length measured at each study visit
3.5 months
Recall of stool consistency measured at each study visit
3.5 months
Medically-confirmed adverse events collected throughout the study period
3.5 months
Head circumference measured at each study visit
3.5 months
- +2 more secondary outcomes
Study Arms (2)
Infant formula containing an alternate source of DHA
EXPERIMENTALMarketed routine infant formula
ACTIVE COMPARATORInterventions
Eligibility Criteria
You may qualify if:
- Singleton, 10-14 days of age at randomization
- Term infant with birth weight of a minimum of 2500 grams
- Solely formula fed
- Signed Informed Consent and Protected Health Information
You may not qualify if:
- History of underlying metabolic or chronic disease or immunocompromised
- Feeding difficulties or formula intolerance
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (22)
Birmingham Pediatric Associates
Birmingham, Alabama, 35205, United States
Greenvale Pediatrics - Hoover
Birmingham, Alabama, 35244, United States
Southeastern Pediatric Association
Dothan, Alabama, 36305, United States
Pediatrics East - Alabama Clinical Therapeutics
Pinson, Alabama, 35126, United States
Northwest Arkansas Pediatric Clinic
Fayetteville, Arkansas, 72703, United States
The Children's Clinic of Jonesboro, P.A.
Jonesboro, Arkansas, 72401, United States
Norwich Pediatric Group, PC
Norwich, Connecticut, 06360, United States
Children's Research, LLC
Altamonte Springs, Florida, 32701, United States
Physician Care Clinical Research
Sarasota, Florida, 34239, United States
Deaconess Clinical Research
Evansville, Indiana, 47725, United States
Owensboro Pediatrics
Owensboro, Kentucky, 42303, United States
Woburn Pediatic Associates
Woburn, Massachusetts, 01801, United States
Cary Pediatric Center
Cary, North Carolina, 27511, United States
Capital Pediatrics & Adolescent Center
Raleigh, North Carolina, 27609, United States
Pediatric Associates of Mt. Carmel, Inc
Cincinnati, Ohio, 45245, United States
Pediatric Associates of Fairfield, Inc.
Fairfield, Ohio, 45014, United States
UHMP Comprehensive Pediatrics
Westlake, Ohio, 44145, United States
Coastal Pediatric Research
Charleston, South Carolina, 29414, United States
The Jackson Clinic - North Jackson
Jackson, Tennessee, 38305, United States
Holston Medical Group
Kingsport, Tennessee, 37660, United States
Austin Diagnostic Clinic
Austin, Texas, 78745, United States
DCOL Center for Clinical Research
Longview, Texas, 75605, United States
Related Publications (1)
Yeiser M, Harris CL, Kirchoff AL, Patterson AC, Wampler JL, Zissman EN, Berseth CL. Growth and tolerance of infants fed formula with a new algal source of docosahexaenoic acid: Double-blind, randomized, controlled trial. Prostaglandins Leukot Essent Fatty Acids. 2016 Dec;115:89-96. doi: 10.1016/j.plefa.2016.09.001. Epub 2016 Sep 29.
PMID: 27914519DERIVED
Study Officials
- STUDY DIRECTOR
Carol Lynn Berseth, M.D.
Mead Johnson and Company
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 5, 2014
First Posted
May 7, 2014
Study Start
May 1, 2014
Primary Completion
March 1, 2015
Study Completion
April 1, 2015
Last Updated
May 1, 2015
Record last verified: 2015-04