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The Effects of Study Products Containing Varying Quantities of Docosahexaenoic Acid (DHA)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01174134
Enrollment
Unknown
Registered
2010-08-03
Start date
2006-07-31
Completion date
Unknown
Last updated
2011-09-02

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

Conditions

Levels of DHA in the Blood

Brief summary

The clinical trial will provide a milk-based drink with constant amounts of nutrients but differing amount of Docosahexaenoic Acid (DHA).

Interventions

Sponsors

Mead Johnson Nutrition
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Months to 36 Months
Healthy volunteers
Yes

Inclusion criteria

* Participant is 18 to 36 months of age * Participant's current weight and height within the 10th to 90th percentiles * Parent/caregiver reports that participant consumes milk or a milk-based beverage on a daily basis * Participant lives at home with parent(s) or other family member(s) * Signed informed consent and authorization obtained to use and or disclose Protected Health Information (PHI)

Exclusion criteria

* Participant who is receiving any breast milk at time of randomization * Participant with an active infection. * Participant with a history of underlying disease, chronic disease, or congenital malformation which in the opinion of the Investigator is likely to interfere with the evaluation of the participant. * Known or suspected intolerance to cow's milk protein * Participant diagnosed with diabetes * Participant is from a multiple birth and the sibling(s) are still living * Participant with a sibling that has participated in this study.

Design outcomes

Primary

MeasureTime frame
Blood lipid levels of Docosahexaenoic Acid (DHA) at enrollment and after two months, assessment of usual DHA intake, and product acceptability and use

Secondary

MeasureTime frame
Growth
Determination of nutrient status, including iron and vitamin D status
Adverse Events

Countries

United States

Outcome results

None listed

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