Phase
Condition
Dementia
Memory Loss
Alzheimer's Disease
Treatment
Placebo Control
Broccoli sprout extract (BSE)
Clinical Study ID
Ages 50-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age: Adults aged 55-85 years (inclusive), both male and female
Global Deterioration Scale (GDS) score of 2-3:
GDS 2: Subjective memory impairment without objective evidence GDS 3: Mild objective memory impairment
Absence of dementia according to established diagnostic criteria
Ability to read Korean
Exclusion
Exclusion Criteria:
Severe medical conditions within the past 6 months: History of severecerebrovascular disease (cerebral infarction, cerebral hemorrhage), cardiac disease (angina, myocardial infarction, heart failure, arrhythmia requiring treatment), ormalignancy (Note: Participants with a history of cerebrovascular or cardiac diseasewho are clinically stable may be included at the investigator's discretion)
Cognitive impairment-associated diseases: Dementia, Parkinson's disease, cerebralinfarction, or other conditions associated with cognitive decline Uncontrolledhypertension: Blood pressure ≥160/100 mmHg (measured after 10 minutes of rest)
Poor glycemic control: Fasting blood glucose ≥160 mg/dL in diabetic patients
Uncontrolled thyroid dysfunction: Currently receiving treatment for uncontrolledhypothyroidism or hyperthyroidism
Renal impairment: Serum creatinine ≥2 times the upper limit of normal for theinstitution
Hepatic impairment: AST or ALT ≥2 times the upper limit of normal for theinstitution
Severe gastrointestinal symptoms: Complaints of severe heartburn, dyspepsia, orother gastrointestinal distress
Medications affecting cognitive function within the past month: Use of drugs (antipsychotics, anti-degenerative agents, cognitive enhancers, tricyclicantidepressants, hormone replacement therapy) or health functional foods that mayinfluence cognitive function due to dementia or other cognitive abnormalities
Other clinical trial participation: Participation in other drug clinical trialswithin the past month or planned participation during the study period
Alcohol use disorder, severe
Food allergies: Known allergic reactions to study product components
Investigator discretion: Any other condition deemed inappropriate for studyparticipation by the investigator
Study Design
Study Description
Connect with a study center
Pusan National University Yangsan Hospital
Yangsan 1832828, 50612
South KoreaActive - Recruiting

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