Effects of administrating of test foods for 8 weeks on skin condition in subjects

Not Applicable

Completed

• Conditions: Healthy subjects

• Registration Number: JPRN-UMIN000028510
• Lead Sponsor: House Wellness Foods Corporation Research and Development Institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-08-08
• Last Update Posted: 2023-10-17

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 45

Inclusion Criteria

Not provided

Exclusion Criteria

Those who 1)have been diagnosed with photosensitivity 2)taking drugs that affect the light sensitivity of the skin 3)taking drugs, quasi-drugs, health foods, supplements that emphasizes or promotes efficacy related to the effectiveness examined in this study or joint pain improvement 4)were judged to have a skin disease of the evaluation site by the doctor 5)are using drugs or quasi-drugs that may affect the results of the trial 6)already regularly use cosmetics, foods or supplements that may affect the results of the trial 7)drinks much alcohol, or are heavy smokers 8)have risk of allergies to drugs and foods 9)are hospitalized in dermatology department 10)have factors that may affect the results of the trial on the evaluation site 11)have subjective symptoms of advanced anemia 12)receiving medical treatment at a medical institution for treatment or prevention of diseases, or judged to be in a condition requiring treatment 13)have past or current medical history 14)have received skin care treatment or massage for the evaluation site within the past 4 weeks or are scheduled to receive during the trial period 15)have been exposed to UV beyond daily living such as long-term work outdoors, exercise, sea bathing, tanning salon, etc. during the past 2 months, or planned during the trial period 16)have irregular or disturbed life rhythms such as night shifts and shift work 17)are participating in other trial, have participated in the past 4 weeks or plan to participate in other trial during scheduled period in this trial. 18)are difficult to maintain lifestyle during the trial period 19)are lactating at the time of consent acquisition, pregnant or may be pregnant, or wish to be pregnant during the trial period 20)are difficult to menstruation 21)are difficult to fill in the subject diary 22)are judged inappropriate for participating in the trial by the doctor or investigator of this trial

Study & Design

• Study Type: Interventional
• Study Design: Not specified