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NCT00753818 Clinical Trial

Developmental Effects of Infant Formula Supplemented With LCPUFA

Growth Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00753818
Other study ID # 3370-2(-4)
Secondary ID
Status Completed
Phase N/A
First received September 16, 2008
Last updated September 16, 2008

Study information
Verified date September 2008
Source Mead Johnson Nutrition
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the effects on visual development, growth, cognitive development, tolerance, and blood chemistry parameters in term infants fed one of four study formulas containing various levels of DHA and ARA.

Other known NCT identifiers
  • NCT00222157

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A to 5 Days
Eligibility Inclusion Criteria:

- healthy, term, formula fed infants from 1-5 days of age

Exclusion Criteria:

- history of disease that effects normal growth and development

- breast fed, or formula intolerance

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Other:
• DHA and ARA
various levels of DHA and ARA
• Control

Locations
Country Name City State
United States The University of Texas Southwestern Medical Center at Dallas Dallas Texas
United States The University of Kansas Medical Center Kansas City Kansas

Sponsors (1)
Lead Sponsor Collaborator
Mead Johnson Nutrition

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary visual development
Secondary Cognitive development
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