Verification of improvement effects on skin function by test-food consumption - Verification of improvement effects on skin function by test-food consumption

CPCC Company Limited0 sites80 target enrollmentSeptember 12, 2023

ConditionsHealthy female adults

Overview

Phase: 未知
Intervention: Not specified
Conditions: Healthy female adults
Sponsor: CPCC Company Limited
Enrollment: 80
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

September 12, 2023

End Date

April 19, 2023

Last Updated

2 years ago

Study Type

Interventional

Sex

Female

Investigators

Sponsor

CPCC Company Limited

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

•Subjects \- \- (1\) who take steadily (over 3 times a week) in affecting health\-specific/functional/supplementary/health foods, (2\) who have taken affecting medicines and quasi\-ones (e.g., skin medicine for external use), over 3 times a week, and have any difficulty in refraining from taking them, (3\) with excessive suntan, or planning to tan on trips, events, etc., (4\) planning to change their cosmetics, (5\) planning to newly begin their skin cares, (6\) suffering from some kind of skin disease (e.g., atopic dermatitis), (7\) having a bruise and/or a hurt near the skin\-measuring position, (8\) who are now under a specific care near the skin\-measuring position (e.g., facial treatment, electric facial, peeling, body care, laser therapy, and hair removal) at an outside agency, (9\) with excessive alcohol intake, (10\) having mushrooms, over 5 days a week, (11\) having livers, over 5 days a week, (12\) being poor at mushrooms, (13\) having their skin roughness due to pollinosis, (14\) who realized being in a failing skin condition by menstruation, (15\) having an irregular life rhythm with irregular shift work or midnight one, (16\) being under other clinical tests with medicine or health food, or partook in those within four weeks to this trial, or planning to join those after giving informed consent, (17\) planning to change their shapes of eyelashes/eyebrows, (18\) having previous/current medical history of severe cardiac, hepatic, renal or digestive diseases, (19\) with pregnancy, possibly one, or lactating, (20\) with drug and food allergy, (21\) who donated over 0\.2 L of their blood and/or blood components within a month to this trial, (22\) who donated their whole blood (0\.4 L) within the last four months to this trial, (23\) who will be collected in total of their blood (0\.8 L) within the last twelve months, after adding the blood amounts planning to be sampled in this trial, (24\) being determined as ineligible for participation, judging from the principal/sub investigator \- \- .