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Clinical Trial Summary

The objective of the study is to assess gastrointestinal tolerance and compliance in infants who require a hydrolyzed formula.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01573871
Study type Interventional
Source Abbott Nutrition
Contact
Status Completed
Phase Phase 3
Start date February 2012
Completion date September 2012

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