Allergy and Asthma Following Children Who Were Fed Supplemented Infant Formula

August 22, 2008 updated by: Mead Johnson Nutrition
Long-term cognitive outcome study of children who participated in randomized trials of LCP-supplemented formula during infancy.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Texas
      • Dallas, Texas, United States, 75231
        • Retina Foundation of the Southwest

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

5 days to 1 year (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Study Population

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

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

What is the study measuring?

Primary Outcome Measures

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Mead Johnson Nutrition

Collaborators

National Institutes of Health (NIH)

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted

August 22, 2008

First Submitted That Met QC Criteria

August 22, 2008

First Posted (Estimate)

August 25, 2008

Study Record Updates

Last Update Posted (Estimate)

August 25, 2008

Last Update Submitted That Met QC Criteria

August 22, 2008

Last Verified

August 1, 2008

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 8580

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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