MedPath

Effects of a Plant-Derived Test Food for Improvement of Skin Functio

Not Applicable
Conditions
/A(healthy adults)
Registration Number
JPRN-UMIN000030264
Lead Sponsor
TES Holdings Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
70
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 use a drug to treat a disease in the past 1 month. [5]Individuals who contract or have a history of serious hepatopathy, kidney damage, heart disease and blood disease. [6]Individuals who contract or have a history of serious endocrine disease. [7]Individuals with serious anemia. [8]Individuals who are sensitive to dairy products. [9]Individuals who are sensitive to a test producer other foods, and medical products. [10]Individuals who are or are possibly, or are lactating. [11]Individuals who are alcoholism or mental disorders. [12]Individuals who have a habit of smoking. [13]Individuals whose life style will change during the test period. [14]Individuals with probable seasonal allergy, such as pollinosis, during the test period. [15]Individuals who are busy to their own work, housework or child care and neglect skin care. [16]Individuals who will get sunburned during the test period (including winter sports like skiing and snowboarding). [17]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. [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 in the past 6months. [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]Indexes for skin functions (skin moisture content, transepidermal water loss, and visual evaluation) (Week 0, Week 6 and Week 12).
Secondary Outcome Measures
NameTimeMethod
*Safety evaluation [1]Doctor's questions (Week 0, Week 6 and Week 12). *Other indexes [1]Subject's diary (From the first day of ingestion of a test material to the last day of the test).
© Copyright 2025. All Rights Reserved by MedPath