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Whitening effect of the supplement and cosmetics when used alone compared to simultaneously

Whitening effect of the supplement and cosmetics when used alone compared to simultaneously - Whitening effect of the supplement and cosmetics when used alone compared to simultaneously

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000034004
Enrollment
60
Registered
2018-09-03
Start date
2018-09-04
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy person

Interventions

Test food (Intake priod:12 weeks) Test cosmetics (use priod:12 weeks) Test food and Test cosmetics (use priod:12 weeks)

Sponsors

FANCL Corporation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1)Japanese healthy females aged 35 to 54 years at the time of informed consent. 2)Healthy subjects who do not have chronic physical disorders,including skin diseases. 3)Subjects who have senile pigment freckle on face. 4)Subjects who agree to participate in the study on one's own will. 5)Subjects who can visit the designated medical institution on specified date during the study. 6)Subjects who are judged as reasonable participants for the study by the doctor in charg.

Exclusion criteria

Exclusion criteria: 1)Subjects who have certain diseases and undergoing drug treatment on medication. 2)Subjects who are currently using medication. 3)Subjects who have taken medicines for the purpose of treating diseases within the past one month. 4)Subjects who are suffering or suffered from serious disease. 5)Subject who have skin disease. 6)Subjects who have sensitive skin. 7)Subjects who have severe skin disorders on the face. 8)Subjects who have mole, acne vulgaris, erythema, capillary dilation at the measurement points. 9)Subjects who have may show allergic symptoms to cosmetics. 10)Subjects who may show severe allergic symptoms to the test foods. 11)Subjects who have alcoholism or other psychiatric disorders. 12)Subjects who have smoking habit. 13)Subjects who may change lifestyle habits during the test period. 14)Subjects who are unable to refrain from direct sunlight, during the test period. 15)Subjects who develop pollinosis and may use medication during the study period. 16)Subjects who used or will use of medications, health foods, supplements, which have skin whitening and skin improvement effects during the test period, or who have used any of the above within the past 3 months. 17)Subjects who used cosmetics or medication that may advocate the whitening effect within the past 3 months or who are planning to use them during the test period. 18)Subjects who had treatment history at the evaluation site within the past 6 months. 19)Subjects who are pregnant or breast-feeding. 20)Subjects who are participating in other clinical studies or who have participated in other clinical studies within the past 3 months. 21)Subjects who or whose family work for a company that develops, manufactures or sells health foods, and cosmetics. 22)Subjects who are judged as unsuitable participant for the study by the doctor and the investigator in charge for other reasons.

Design outcomes

Primary

MeasureTime frame
Skin color quantification by spectrophotometer Skin color evaluation by skin color scale

Secondary

MeasureTime frame
VISIA image analysis Questionnaire

Countries

Japan

Contacts

Public ContactRyoma Shimizu

TES Holdings Co., Ltd Administrative Department of Clinical Trials

r.shimizu@tes-h.co.jp+81-3-6801-8480

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026