Followup of Infants Fed Non-routine Infant Formula

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00665938

Enrollment

183

Registered

2008-04-24

Start date

2006-10-31

Completion date

2011-12-31

Last updated

2012-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Physical development

Brief summary

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

Interventions

OTHERInfant formula

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

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Masking

TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender

ALL

Age

4 Months to 4 Months

Healthy volunteers

Yes

Inclusion criteria

* Completed Study 3369-5

Exclusion criteria

* None

Design outcomes

Primary

Measure	Time frame
Achieved weight	5 years

Secondary

Measure	Time frame
Tolerance	1 year

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026