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OpenTrials
Completed

NCT Number: NCT00366873

Evaluation of Mineral Absorption in Infants Fed Infant Formula

The purpose of this study is to measure calcium absorption in infants fed formula with and without prebiotics.

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Key information

Conditions

Age range

56 day–70 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fomon Infant Nutrition Unit, Coralville, Iowa, United States

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About this study

Infants will be fed formula and blood drawn and urine collected to measure calcium absorption.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy, term infants

Exclusion criteria

  • Breast fed infants
  • Use of vitamin/mineral supplements
  • Currently on medication

Treatment and study plan

Calcium absorption

Procedure

formula with or without prebiotics

Primary outcomes

  1. Calcium absorption

    Time frame: 14 days

Secondary outcomes

  1. Vitamin D levels

    Time frame: 14 days

Sponsors and collaborators

Lead sponsor

Mead Johnson Nutrition

Industry

Registry information

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Aug 21, 2006
Registry last updated
Mar 5, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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