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Evaluation of Mineral Absorption in Infants Fed Infant Formula

Not Applicable
Completed
Conditions
Mineral Absorption in the Urine
Interventions
Other: Infant Formula
Registration Number
NCT01177917
Lead Sponsor
Mead Johnson Nutrition
Brief Summary

This clinical trial will help determine if prebiotics can increase mineral absorption in babies

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Singleton
  • Term infant
  • Birth weight of 2500 g or more
  • 56-70 days of age
  • Signed informed consent
  • Consuming a cow's milk-based infant formula for at least 24 hours.
Exclusion Criteria
  • History of underlying disease or congenital malformation which, in the opinion of the Investigator, is likely to interfere with the normal growth and development or the evaluation of the mineral absorption of the participant
  • Use of multiple vitamin and mineral supplements prior to enrollment.
  • Evidence of formula intolerance or poor intake at time of randomization

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Cow milk-based infant formula with prebiotic blendInfant Formula-
Marketed Cow milk-based infant formulaInfant Formula-
Primary Outcome Measures
NameTimeMethod
To evaluate the amount of minerals in the urine
Secondary Outcome Measures
NameTimeMethod
Compare the amount of vitamins and minerals in the blood

Trial Locations

Locations (5)

The Center for Human Nutrition

🇺🇸

Omaha, Nebraska, United States

Children's Research and Nutrition Center

🇺🇸

Houston, Texas, United States

Cincinnati Children's Hospital Medical Center Clinical Trials Office

🇺🇸

Cincinnati, Ohio, United States

Pediatric Clinical Trials Unit

🇺🇸

Louisville, Kentucky, United States

Children's Hospital of Iowa

🇺🇸

Coralville, Iowa, United States

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