Followup of Infants Fed Non-routine Infant Formula

The purpose of this study is to compare physical development of infants fed one of three study formulas.

Completed

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Key information

Conditions

Healthy

Age range

4 month–4 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Completed Study 3369-5

Exclusion criteria

None

Treatment and study plan

Infant Formula

Other

Arm 1. extensively hydrolyzed infant formula without probiotics (Nutramigen LIPIL)

Arm 2. partially hydrolyzed infant formula with probiotics

Arm 3. extensively hydrolyzed infant formula with probiotics

Other names: No other names are applicable to the 3 intervention arms

Primary outcomes

Achieved weight

Time frame: 5 years

Secondary outcomes

Tolerance

Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Mead Johnson Nutrition

Industry

Registry information

Important dates

Study start: 2006
Primary completion: 2011
Study completion: 2011
First posted: Apr 24, 2008
Registry last updated: Jan 31, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed