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A 12week, Multi-center, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the evaluation of the efficacy and safety of AGE2 on the Mild Cognitive Impairment

A 12week, Multi-center, Randomized, Double-blind, Placebo-Controlled Clinical Trial for the evaluation of the efficacy and safety of AGE2 on the Mild Cognitive Impairment

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004574
Enrollment
100
Registered
2019-12-20
Start date
2019-08-14
Completion date
Unknown
Last updated
2020-01-14

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

Conditions

None listed

Interventions

Dietary Supplement : Treatment(KE_AGE2, combined Aster glehni extracts 960mg/day) gourp: Take 1 tablet 2 times per day with water for 12 weeks Control (Placebo): Same way with treatment

Sponsors

Koreaeundan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Adult men and women aged from 55 t0 85 years old who complain memory loss 2) Those who can decipher Korean 3) CERAD-K memory score decreased from 1.0SD to less than 2.0SD compare to the same age and education level gruop (CERAD word list memory or word delayed recall or word recognition) 4) A person who agrees to participate in the test and has signed an informed consent form

Exclusion criteria

Exclusion criteria: 1) A person who is admitted to hospital with malignant tumor, severe cerebrovascular disease (cerebral infarction, cerebral hemorrhage, etc.), severe heart disease (unstable angina, myocardial infarction, arrhythmia requiring heart failure treatment) or 3 months after discharge 2) A person with disease causing cognitive impairment such as dementia, Parkinson's disease,cerebral infarction etc. 3) A person who has experience of administering drugs (antipsychotic drugs, degenerative disease agents, brain function improvers, tricyclic antidepressants) for dementia or other cognitive dysfunction within 4 weeks 4) A person whose daily dose of vitamin E preparation is 400 IU or more, or whose dosage decreasing is inevitable. 5) A person who have received estrogen replacement therapy (excluding topical application agents) within 2 months of the start of the test

Design outcomes

Primary

MeasureTime frame
Alzheimer’s Disease Assessment Scale-Korean version-Cognitive subscale total score

Secondary

MeasureTime frame
Alzheimer’s Disease Assessment Scale-Korean version-Cognitive subscale memory score

Countries

Korea, Republic of

Contacts

Public ContactJae-eun Jeong

Neonutra

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026