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Assessment of Feeding Tolerance in Infants Fed Cow Milk Formula

NCT00666120 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 333

Last updated 2008-04-24

No results posted yet for this study

Summary

To compare the number of infants who discontinue from study formula due to formula intolerance as documented by the investigator.

Hypothesize there will be no difference between formula groups.

Conditions

  • Healthy Term Infants Solely Formula Fed

Interventions

OTHER

Enfamil LIPIL with iron

cow's milk based infant formula

OTHER

Good Start Supreme with DHA and ARA

partially hydrolzed cow's milk protein

Sponsors & Collaborators

  • Mead Johnson Nutrition

    lead INDUSTRY

Principal Investigators

  • Carol Berseth, MD · Mead Johnson Nutrition

Study Design

Allocation
RANDOMIZED
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
4 Days
Max Age
18 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-06-30
Primary Completion
2006-04-30
Completion
2006-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00666120 on ClinicalTrials.gov