Brain Imaging Study

Completed · Not applicable · Has a placebo group

Conditions studied: Brain Health

In brief

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.

Key facts

Study ID

NCT02439983

Run by

Pharmanex

People needed

68

Starts

2015-04-01

Expected to finish

2016-06-01

Last updated by the study team

2016-08-03

Who can join

Age: 40 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• University of Utah - Brain Institute — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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