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Allergy and Asthma Following Children Who Were Fed Supplemented Infant Formula

Primary Purpose

Allergy, Asthma

Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by
Mead Johnson Nutrition
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for Allergy

Eligibility Criteria

5 Days - 12 Months (Child)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Retina Foundation of the Southwest

Outcomes

Primary Outcome Measures

Prevalence of asthma and allergy related diagnosis in medical records during first 3 years of life.

Secondary Outcome Measures

Full Information

First Posted
August 22, 2008
Last Updated
August 22, 2008
Sponsor
Mead Johnson Nutrition
Collaborators
National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00740974
Brief Title
Allergy and Asthma Following Children Who Were Fed Supplemented Infant Formula
Study Type
Observational

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators

Name of the Sponsor
Mead Johnson Nutrition
Collaborators
National Institutes of Health (NIH)

4. Oversight

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergy, Asthma

7. Study Design

Primary Outcome Measure Information:
Title
Prevalence of asthma and allergy related diagnosis in medical records during first 3 years of life.
Time Frame
after first 3 years of life

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Days
Maximum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Study Population Description
children previously randomized in a clinical study consuming LCP-supplemented infant formula
Facility Information:
Facility Name
Retina Foundation of the Southwest
City
Dallas
State/Province
Texas
ZIP/Postal Code
75231
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Allergy and Asthma Following Children Who Were Fed Supplemented Infant Formula

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