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Evaluation study for intake of cyclic dipeptide on improvements in cognitive function

Evaluation study for intake of cyclic dipeptide on improvements in cognitive function - Evaluation study for intake of cyclic dipeptide on improvements in cognitive function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057140
Enrollment
60
Registered
2025-02-28
Start date
2025-02-21
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Intake cyclic dipeptide for 12 weeks Intake placebo for 12 weeks

Sponsors

Shiba Palace Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Japanese males and females aged 60 to 75 years old at the time of informed consent 2) Subjects who feel that they are more forgetful compared with their younger days

Exclusion criteria

Exclusion criteria: 1) Subjects judged inappropriate for the study by the principal 2) Subjects who are participating in other clinical trials 3) Subjects who are taking medicines that can affect the test result 4) Subjects who are taking supplements that can affect the test result 5) Subjects who took RBANS by 3 months before the start of the test 6) Subjects who can be allergic to the test food 7) Subjects who have had a stroke, subarachnoid hemorrhage, cerebral infarction, cerebral hemorrhage, cerebral contusion, or head injury resulting in hospitalization for treatment or surgery 8) Excessive tobacco and alcohol users and those with extremely irregular eating habits 9) Subjects with medical history of hepatitis 10) Subjects with severe anemia 11) Subjects with medical history or medical treatments of Epileptic seizures, diabetes, thyroid dysfunction, or severe renal dysfunction (hemodialysis, uremia, anuria) 12) Subjects who have taken neuropsychological tests in the hospital

Design outcomes

Primary

MeasureTime frame
RBANS Cognitrax (before and 12 weeks after intake)

Secondary

MeasureTime frame
SF-36v2 WHO-5J body mass and BMI blood pressure, pulsation subjects' diary doctor's questions (before and 12 weeks after intake)

Countries

Japan

Contacts

Public ContactMiwa Kaneko

SOUKEN Co., Ltd Management Division

jimukyoku@mail.souken-r.com03-5408-1555

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026