Citicoline Effects on Cortical Membrane Structure and Function
Completed · Not applicable · Has a placebo group
Conditions studied: Healthy
In brief
The goal of this project is to determine the effects of 6-week dietary supplementation with one of two doses of citicoline (250 mg/d, 500 mg/d) or placebo on prefrontal cortical membrane dynamics (31P-MRS) and event-related functional activation (fMRI) in healthy middle-aged adults.
Key facts
- Study ID
- NCT02705066
- Run by
- Kyowa Hakko Bio Co., Ltd.
- People needed
- 61
- Starts
- 2016-03-01
- Expected to finish
- 2018-07-01
- Last updated by the study team
- 2019-05-23
Who can join
Age: 40 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Provision of written informed consent;
- Ages 40-60 years old;
- Right handed.
- If female, not pregnant (as determined by a positive pregnancy test); and agrees to use one of the following methods of birth control: abstinence from sexual intercourse, barrier (diaphragm or condom), or oral/injectable contraceptive;
You may not qualify if…
- Contraindication to an MRI scan (i.e., braces, claustrophobia, pacemaker etc);
- A history of a major medical (e.g., diabetes) or neurological illness (e.g., epilepsy);
- Body mass index (BMI) ≥ 30;
- An IQ <75 and >130;
- A positive urine drug test (nicotine dependence is permitted);
- Personal history of a DSM-5 Axis I psychiatric disorder;
- Requiring treatment with a drug which might obscure the action of the study treatment.
Where it is running
- University of Cincinnati — Cincinnati, Ohio, United States
Full record on ClinicalTrials.gov
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