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Study on the accumulation of AGEs by test food intake

Not Applicable
Conditions
Healthy volunteer
Registration Number
JPRN-UMIN000030691
Lead Sponsor
Anti-Aging Bank Co.,Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
24
Inclusion Criteria

Not provided

Exclusion Criteria

[1]Individuals using medical products [2]Individuals with skin disease,such as atopic dermatitis [3]Individuals who have an inflammation or a scar on a measuring area [4]Individuals under treatment or with history of mental disorders, sleep disorders,hypertension,diabetes,lipid metabolism abnormality,or other serious disorders [5]Individuals receiving/received medical drug treatment for the past 1 month except for temporary relief medication for headache,menstrual pain,common cold,etc. [6]Individuals with history of serious diseases (hepatic,renal,cardiovascular,respiratory,hematologic,etc.) [7]Individual who have digestive organ disease [8]Individuals donated blood >200ml in past 1 month or >400ml in past 3 months [9]Individual who have experienced mood disorder or physical condition deterioration due to blood sampling in the past [10] Individuals deemed sensitive to the test product or highly allergic to foods or medical drugs [11]Currently,health food,supplements with continuous ingestion habits,individuals who intend to intake during the examination period (but not those who can stop taking the intake at the time of consent acquisition) [12]Individuals with alcohol intake exceeding 60g/day,as ethanol volume [13]Individuals who may significantly change exercise habit or lifestyle during the study period(ex. travel for a long time) [14]Pregnant or lactating women (expected,desired inclusive) [15]Individuals who will get sunburned during the test period etc. [16]Individuals participating or planning to join the other clinical investigations during the study period [17]Individual with potential conflict of interests [18]Individuals judged inappropriate for the study by the principal

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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