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The Effects on Growth of a Non-Routine Infant Formula

NCT00655720 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 293

Last updated 2008-04-15

No results posted yet for this study

Summary

A study to evaluate the growth and development of term infants fed either an extensively hydrolyzed formula with probiotics, a partially hydrolyzed formula with probiotics, or an extensively hydrolyzed formula without probiotics

Conditions

  • Growth

Interventions

OTHER

infant formula

1. hydrolyzed infant formula without probiotics 2. hydrolyzed infant formula with probiotics 3. hydrolyzed infant formula with probiotics

Sponsors & Collaborators

  • Mead Johnson Nutrition

    lead INDUSTRY

Principal Investigators

  • Deolinda Scalabrin, MD · Mead Johnson Nutrition

Study Design

Allocation
RANDOMIZED
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
12 Days
Max Age
16 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-03-31
Primary Completion
2007-05-31
Completion
2007-05-31

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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 NCT00655720 on ClinicalTrials.gov