NCT07089238 Evaluate the Effects of Citicoline on Mood in Healthy Adults
| NCT ID | NCT07089238 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Kirin Holdings Company, Limited |
| Condition | Healthy |
| Study Type | INTERVENTIONAL |
| Enrollment | 90 participants |
| Start Date | 2025-07-31 |
| Primary Completion | 2026-03-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 90 participants in total. It began in 2025-07-31 with a primary completion date of 2026-03-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The objective of this trial is to determine the effects of citicoline on mood in healthy Men and Women compared to a placebo.
Eligibility Criteria
Inclusion Criteria: * Provide voluntary signed and dated informed consent. * Be in good health and able to participate as determined by medical history and routine blood chemistries. * Biological men and women between 21 and 65 years of age (inclusive). * Body Mass Index of 18.5-32.0 (inclusive). * Body weight of at least 110 pounds. * Participant is experiencing moderate levels of mood disturbance during screening. * Normotensive (seated, resting systolic blood pressure \<140 mm Hg and diastolic blood pressure \< 90 mm Hg. * Normal supine, resting heart rate (\<90 per minute). * Agrees to maintain their existing dietary and physical activity patterns throughout the study period. * Participants agree to maintain their usual caffeine consumption habits, given that they do not exceed the maximum intake per day (400mg/day or 3-4 cups of coffee per day). * If a dietary supplement was initiated within the past month, the participant is willing to discontinue supplement use followed by a 2-week washout prior to participation in the study. * Willing to duplicate their previous 24-hour diet, refrain from caffeine for 24 hours, refrain from alcohol and exercise for 24 hours prior to each trial, and fast for 10 hours prior to each visit. Exclusion Criteria: * QIDS (Quick Inventory of Depressive Symptomology) score \> 16. * Women who are pregnant, lactating, or planning to become pregnant during the study. Women must have a negative pregnancy test at screening. * Women with a PSST (Premenstrual Symptoms Screening Tool) score ≥30 * Current smokers or cessation within 3 months prior to screening. * Alcohol consumption (\>2 standard alcoholic drinks/day or \>10 drinks/week) or drug abuse/dependence. * Current use of any nootropic dietary supplements (e.g., GABA, Ashwaghanda, St. John's Wort, Ginkgo biloba, L-theanine, choline, Lion's mane, creatine, etc.) or medications (e.g., piracetam, Adderall, modafinil, etc.) that may confound the study or its endpoints. * Medical history of hepatorenal, musculoskeletal, autoimmune, or neurologic disease. * Individuals who have been diagnosed with digestive, liver, renal, cardiovascular, or other metabolic diseases. * Other known gastrointestinal or metabolic diseases that might impact nutrient absorption, distribution, metabolism, or excretion (e.g., intestinal malabsorption, electrolyte abnormalities, diabetes, thyroid disease, adrenal disease, hypogonadism, short bowel syndrome, diarrheal illnesses, history of colon resection, gastric ulcer, reflux disease, gastroparesis, Inborn-Errors-of-Metabolism, etc.). * Chronic medically diagnosed inflammatory condition or disease (e.g., rheumatoid arthritis, Crohn's disease, ulcerative colitis, Lupus, HIV/AIDS, etc.). * Medical history of a cognitive (i.e., ADD/ADHD) or psychiatric disorder, or brain-related medical conditions (e.g., TBI, ADHD). * Currently using medications to treat anxiety or depression. * Have an irregular sleep pattern (i.e. shift workers) or inadequate sleep schedule (i.e., less than 6 hours per night). * Known sensitivity, allergy, or intolerability to any ingredient in the test products. * Participants who report a clinically significant illness within the last 30 days. * Individuals who are cognitively impaired and/or who are unable to give informed consent. * Any other diseases or conditions that, in the opinion of the Principal Investigator, could confound the primary endpoint or place the subject at increased risk of harm if they were to participate.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07089238 clinical trial?
This trial is open to participants of all sexes, aged 21 Years or older, up to 65 Years, studying Healthy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07089238 currently recruiting?
Yes, NCT07089238 is actively recruiting participants. Contact the research team at tz@appliedhealthsciences.org for enrollment information.
Where is the NCT07089238 trial being conducted?
This trial is being conducted at Canfield, United States.
Who is sponsoring the NCT07089238 clinical trial?
NCT07089238 is sponsored by Kirin Holdings Company, Limited. The trial plans to enroll 90 participants.