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Effect of the Test Food on Skin Quality and Endothelial Function.

Not Applicable
Conditions
/A(healthy adults)
Registration Number
JPRN-UMIN000035620
Lead Sponsor
TES Holdings Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
12
Inclusion Criteria

Not provided

Exclusion Criteria

[1]Individuals using medical products. [2]Individuals with skin disease, such as atopic dermatitis. [3]Individuals with strange skin conditions at measurement points. [4]Individuals who used or applied a drug for treatment of disease in the past 1 month. [5]Individuals who have a history of serious hepatopathy, kidney damage, heart disease, hematological and blood disease. [6]Individual who have digestive organ disease. [7]Individuals with serious anemia. [8]Individuals who are sensitive to test product or other foods, and medical products. [9]Individuals who are or are possibly pregnant, or are lactating. [10]Individuals who have an addiction to alcohol or a mental illness. [11]Individuals who are a smoker. [12]Individuals with possible changes of life style during the test period. [13]Individuals with probable seasonal allergy during the test period. [14]Individuals who have severe menopausal symptoms. [15]Individuals who neglect skin care. [16]Individuals who cannot avoid daylight exposure during the test period. [17]Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements containing components of the test product in the past 3 months or will ingest those foods during the test period. [18] Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements in the past 3 months or will ingest those foods during the test period. [19]Individuals who have a habit to use drug claiming to improve skin condition in the past 3 months. [20]Individuals who had been conducted an operation on the test spot. [21] Individuals who have a habit to use drug claiming to improve skin condition in the past 3 months. [22]Individuals judged inappropriate for the study by the principal.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
[1]Skin viscoelasticity (Week 0, Week 4, Week 8).
Secondary Outcome Measures
NameTimeMethod
*Secondary indexes [1]Skin moisture content (Week 0, Week 4, Week 8). [2]Transepidermal water loss (Week 0, Week 4, Week 8). [3]Observation for skin condition by dermatologists (Week 0, Week 4, Week 8). [4]Arterial pressure-volume index, arterial velocity pulse index (Week 0, Week 4, Week 8). [5]Questionnaire of physical feeling (Week 0, Week 4, Week 8). *Safety [1]Weight, body fat percentage, BMI (Week 0, Week 4, Week 8). [2]Doctor's questions (Week 0, Week 4, Week 8). *Other index [1]Subject's diary (each day during the test period).
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