Expired Study
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Salt Lake City, Utah 84108


Purpose:

The study is designed to evaluate the effects of the proprietary nutritional supplement on cognition, mood, and brain imaging parameters following a relatively short period of treatment.


Criteria:

Inclusion Criteria: - Both male and female subjects will be included. - Age between 40-60 years inclusive. - Healthy subjects who, in the opinion of the investigator, are free of any medical conditions that might affect study measures. - Eats 1 or fewer servings of fatty fish per week. - BMI < 35 Exclusion Criteria: - Current or past neurological illness. - Substance abuse or dependence within the prior 60 days. - Current depression (HAMD greater than 20) or anxiety disorder (HAMA greater than 18). - Current or past history of psychiatric disorder. - History of head trauma with loss of consciousness. - Contraindication to brain MRI examination. - Supplementation with Omega 3, fish oil, or other over the counter supplements including the other bioactive ingredients in the proprietary nutritional supplement, antioxidants and multi-vitamin mineral supplements for the previous 3 months. - Plasma Omega3 Index >5% at screening visit. - Subject has a known allergy or intolerance to any of the ingredients contained in the proprietary nutritional supplement or placebo. - Subject is currently pregnant, planning to become pregnant, or is breastfeeding.


NCT ID:

NCT02439983


Primary Contact:

Principal Investigator
Deborah Yurgelun-Todd, Ph.D.
University of Utah


Backup Contact:

N/A


Location Contact:

Salt Lake City, Utah 84108
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 20, 2017

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