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Clinical Trials/NCT00705562
NCT00705562
Completed
Phase 2

Tolerance of Healthy Term Infants Fed Infant Formulas

Abbott Nutrition15 sites in 1 country190 target enrollmentJune 2008
ConditionsInfant, Newborn

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Infant, Newborn
Sponsor
Abbott Nutrition
Enrollment
190
Locations
15
Primary Endpoint
Gastrointestinal tolerance
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The objective of the study is to assess comparative gastrointestinal tolerance of normal term infants to various milk-protein infant formulas.

Registry
clinicaltrials.gov
Start Date
June 2008
End Date
December 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Healthy, term infants; singleton birth; 37-42 weeks of age; \>2490gms at birth; 0-8 days of age

Exclusion Criteria

  • medications/foods/formulas affecting GI tolerance;adverse medical history with possible effect on tolerance or growth

Outcomes

Primary Outcomes

Gastrointestinal tolerance

Time Frame: 0-8 days of age until 28 days of age

Secondary Outcomes

  • GI and intake parameters(0-8 to 28 days of age)

Study Sites (15)

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