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Assessing Early Behavioral Indicators of Formula Tolerance

NCT02340143 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2016-09-14

No results posted yet for this study

Summary

The study is intended to assess the amount of crying and fussiness in infants fed an infant formula containing probiotics.

Conditions

  • Tolerance

Interventions

OTHER

Control

Marketed partially hydrolyzed cow's milk protein infant formula

OTHER

Investigational

Partially hydrolyzed cow's milk protein infant formula with a probiotic

Sponsors & Collaborators

  • Baylor College of Medicine

    collaborator OTHER

  • Mead Johnson Nutrition

    lead INDUSTRY

Principal Investigators

  • Carol Lynn Berseth, M.D. · Mead Johnson Nutrition

Study Design

Allocation
RANDOMIZED
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
14 Days
Max Age
28 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2016-08-31
Completion
2016-08-31

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 NCT02340143 on ClinicalTrials.gov