Allergy and Asthma Following Children Who Were Fed Supplemented Infant Formula

NCT ID: NCT00740974

Last Updated: 2008-08-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Study Classification

OBSERVATIONAL

Brief Summary

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Long-term cognitive outcome study of children who participated in randomized trials of LCP-supplemented formula during infancy.

Detailed Description

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Conditions

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Allergy Asthma

Eligibility Criteria

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Inclusion Criteria

* children previously randomized in a clinical study consuming LCP-supplemented infant formula

Exclusion Criteria

* children who did not previously participate in a randomized clinical study consuming LCP-supplemented infant formula
Minimum Eligible Age

5 Days

Maximum Eligible Age

12 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

Mead Johnson Nutrition

INDUSTRY

Sponsor Role lead

Locations

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Retina Foundation of the Southwest

Dallas, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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8580

Identifier Type: -

Identifier Source: org_study_id