MedPath

Effects of the Test Product for Ski

Not Applicable
Conditions
/A(healthy adults)
Registration Number
JPRN-UMIN000026573
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
40
Inclusion Criteria

Not provided

Exclusion Criteria

[1]Individuals using medical products. [2]Individuals who developed asthma in the past 3 months. [3]Individuals who used or applied a drug for treatment of disease in the past 1 month. [4]Individuals with strange skin conditions at measurement points. [5]Individuals who have a history of serious hepatopathy, kidney damage, heart disease, hematological and blood disease. [6]Individuals who contract or have a history of serious gastrointestinal 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 whose bowel habit is irregular. [13]Individuals with possible changes of life style, such as working a night shift or conducting a long-term travel, during the test period. [14]Individuals with probable seasonal allergy, such as pollinosis, during the test period. [15]Individuals who cannot avoid daylight exposure during the test period. [16]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. [17]Individuals who have a habit to use drug claiming to improve skin condition in the past 3 months. [18]Individuals who use cosmetics having a strong moisturizing effect or improvingg effect for wrinkle. [19]Individuals who had been conducted an operation on the test spot in the past 6months. [20]Individuals who participated in other clinical studies in the past 3 months. [21]Individuals who and whose family work in a company developing or manufacturing functional foods. [22]Individuals judged inappropriate for the study by the principal.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
[1]Transepidermal water loss, skin moisture content, skin viscoelasticity (Week 0, Week 8)
Secondary Outcome Measures
NameTimeMethod
*Secondary outcomes [1]Observation for skin condition by a specialist (Week 0, Week 8) [2]Questionnaire of physical feeling (Week 0, Week 4, Week 8) *Other indexes [1]Diagnosis by doctors (Week 0, Week 8) [2]Subject's diary(From the first day of ingestion of a test material to the last day of the test)
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