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Completed

NCT Number: NCT00518414

The Evaluation of Cow Milk-Based Formulas

Infants will be fed infant formula and blood drawn to measure fatty acid levels in the blood.

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Key information

Conditions

Term Infants

Age range

10 day–18 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Birmingham Pediatric Group, Birmingham, Alabama, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy, term infant
  • 10 to 18 days of age

Exclusion criteria

  • Breast fed infants
  • Infants with formula intolerance

Treatment and study plan

Marketed infant formula with DHA and ARA

Other

Milk-based infant formula with DHA and ARA

Other

Milk-based formula with DHA, ARA, prebiotics

Other

Primary outcomes

  1. Red Blood Cell (RBC) ARA and DHA

    Time frame: 120 Days of age

Secondary outcomes

  1. Phospholipid fatty acids, tolerance

    Time frame: 120 Days of age

Sponsors and collaborators

Lead sponsor

Mead Johnson Nutrition

Industry

Registry information

Official study title

The Evaluation of Cow Milk-Based Formulas - Study A

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Aug 20, 2007
Registry last updated
Sep 28, 2015

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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