The Combination Effect of Citicoline and Omega-3
Completed · Not applicable · Has a placebo group
Conditions studied: Healthy
In brief
The goal of this study is to determine the effects of Citicoline plus Omega-3 or Omega-3 alone versus placebo on attention in non-demented healthy older adults.
Key facts
- Study ID
- NCT03444662
- Run by
- Kyowa Hakko Bio Co., Ltd.
- People needed
- 70
- Starts
- 2018-06-12
- Expected to finish
- 2019-09-03
- Last updated by the study team
- 2019-09-10
Who can join
Age: 55 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 55 years or older
- If female, must be post-menopausal
- Non-demented
- Not depressed
- General health status that will not interfere with the participant's ability to complete the study
- No history of neurological disorder
- Screening laboratory values within normal limits or, if abnormal, deemed clinically insignificant by the investigator
- Sufficient English language skills to complete all testing
You may not qualify if…
- Alzheimer's, Dementia or other neurological disease
- Fish intake of 6 ounce serving once a week 3 months prior to enrollment; Omega-3 supplement intake (e.g. fish oil capsules, cod liver oil, or flaxseed oil) less than 3 months prior to enrollment.
- Citicoline supplementation 3 months prior to enrollment
- Prescriptions medications:
- Anticoagulation therapy: Vitamin K antagonist: warfarin (Coumadin, jantoven), Factor Xa inhibitors: rivaroxaban (xarelto), fondaparinux (arixtra), dibigatran (pradaxa), apixaban (eliquis); Low molecular weight heparins: dalteparin (fragmin), enoxaparin (lovenox)
- Dementia medications (e.g. anticholinesterase inhibitors, memantine)
- Diagnosis of Adult Attention Deficit Disorder (ADD) or Attention Deficit Hyperactivity Disorder (ADHD) and/or taking stimulants (e.g. dextroamphetamine sulfate, methylphenidate HCL, dextroamphetamine Sulf-Saccharate)
- Body Mass Index > 30
- Enrollment in another treatment study
Where it is running
- Oregon Health & Science University — Portland, Oregon, United States
Full record on ClinicalTrials.gov
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