Effects of a test powder on skin conditons

Not Applicable

• Conditions: /A(healthy adults)

• Registration Number: JPRN-UMIN000049979
• Lead Sponsor: Morinaga & Co., Ltd.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-03-22
• Study Start: 2023-08-22
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

Not provided

Exclusion Criteria

1)Individuals using medical products. 2)Individuals who have or are treated skin disease symptoms. 3)Individuals with strange skin conditions at measurement points. 4)Individuals who have a history of serious hepatopathy, kidney damage, heart disease, lung and blood disease. 5)Individuals who contract or have a history of serious gastrointestinal disease. 6)Individuals with alcoholism or a mental illness. 7)Individuals who used or applied a drug for treatment of disease in the past 1 month. 8)Individuals with probable seasonal allergy during the test period. 9)Individuals with food allergy. 10)Individuals with serious anemia. 11)Individuals who are a smoker. 12)Females who are or are possibly pregnant, or lactating. 13)Males who usually shave with a razor. 14)Individuals whose life style will change during the test period. 15)Individuals who will get sunburned during the test period. 16)Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements containing ingredients of the test food(quercetin) in the past 3 months or will ingest them during the test period. 17)Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements that have the function of improving skin condition in the past 3 months or will ingest them during the test period. 18)Individuals who have a habit to use drug claiming to improve skin condition in the past 3 months. 19)Individuals who conducted hormone replacement therapy in the past 6 months. 20)Individuals who have received a cosmetic medicine in the past 6 months. 21)Individuals who were hospitalized and received treatment in the past 6 months. 22)Individuals who participated in other clinical studies within one month of consent for participation in this study or who plan to participate in other clinical studies. 23)Individuals judged inappropriate for the study by the principal.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Indexes for skin conditions (0, 8 weeks after ingestion)