None listed
Conditions
Interventions
Ingestion of the test products containing malted rice (once per a day 8 weeks).
Ingestion of the placebo (once per a day 8 weeks).
Sponsors
TTC Co.,Ltd
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: (1)Females from 20 to 64 years of age. (2)Subjects who are anxious about skin dryness.
Exclusion criteria
Exclusion criteria: (1)Subjects who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements which may influence skin. (2)Subjects who has treated cosmetic care. (3)Subjects who has treated cosmetic care except for measuring sites, or hormonal therapy for one year. (4)Subjects who got a facial, a wash-rag, lost hair on measuring sites for one month ago, or plans these actions. (5)Subjects who a long period of time of work and leisure in the outdoors, the sunburn in the exercise for until one month plans these actions. (6)Subjects who washes the body using a nylon towel which provides strong skin irritation. (7)Subjects who has the wound or inflammatory disease affecting the measuring skin. (8)Subjects who has being excepted to be developed the allergy symptoms on skin. (9)Subjects who feels to trouble by rough skin around a menstruates. (10)Subjects who is employed on a pre-dawn shift or on night duty more than 2 times. (11)Subjects who is planned to go overseas. (12)Subjects who has asthma or the possibility of asthma. (13)Subjects who has treatment or a history of serious disease or affecting a secretion of sex hormones. (14)Subjects having possibilities for emerging allergy related to the study. (15)Subjects having possibilities for emerging allergy related to the study. (16)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on screening test. (17)Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study. (18)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (19)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. (20)Subjects judged as unsuitable for the study by the investigator for other reasons.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Skin moisture content | — |
Secondary
| Measure | Time frame |
|---|---|
| Transepidermal water loss Questionnaire | — |
Countries
Japan
Contacts
Public ContactNoriko Watanabe
TTC Co.,Ltd Clinical Research Planning Department
Outcome results
None listed