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Case study about the effect of plant extract containing food on cognitive function

Case study about the effect of plant extract containing food on cognitive function - Evaluation of the effect of plant extract containing food

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038440
Enrollment
7
Registered
2019-11-01
Start date
2019-11-01
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

Mild Cognitive Impairment

Interventions

Continuous intake of test food for 12 months

Sponsors

FUJI-SANGYO CO.,LTD
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Those who regularly visit a "Brain Care Clinic" and have a confirmed diagnosis of mild cognitive impairment 2) Those who have written consent from the subject himself / herself in writing

Exclusion criteria

Exclusion criteria: 1) Those whose test results of cognitive function are too unstable and severe to determine the effect of the test food 2) Those who already use health supplements similar to the test food 3) Those who use health supplements and pharmaceuticals judged by the investigator that will affect the study 4) Those who are participating in other clinical trials at the start of this study, or who are within 3 months from other clinical trials to participation in this study 5) Those who may develop allergies by taking the test food 6) Those who have digestive system disease, or have undergone operation of digestive tract (except for appendicitis) 7) Patients with present or past history of abnormal glucose metabolism, abnormal lipid metabolism, liver disease, kidney disease, cardiovascular disease, endocrine disease, digestive system disease, immune system disease, and mental illness 8) Those who are judged to be inappropriate as test subjects from laboratory tests and blood pressure measurements 9) Those who wish to become pregnant during the study period, or who are currently pregnant or breastfeeding 10) Any other person judged by the investigator as inappropriate

Design outcomes

Primary

MeasureTime frame
Cognitive function test (MMSE, Cognitrax)

Secondary

MeasureTime frame
Blood and urine test

Countries

Japan

Contacts

Public ContactNorimasa Kobayashi

FUJI-SANGYO CO.,LTD Research and Development Laboratory

kobayashi@fuji-sangyo.co.jp0877-25-3221

Outcome results

None listed

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