Evaluation of glycation index, beauty index, glucose metabolism and liver function improvement from ingestion of test food.
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000037855
- Lead Sponsor
- TTC Co., Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 40
Not provided
(1)smoking subjects (2)subjects who have a habit of drinking more than 4 times a week (3)less than five hours in mean sleep (4)routinely taking foods or medicines which may affect skin or blood glucose (5)BMI more than 30 (6)treatment or a history of serious disease or affecting a secretion of sex hormones (7)diseases which affect this study (8)expected to be developed the allergy symptoms on skin (9)donated > 200 mL of blood within 1 month or > 400 mL within 3 months prior to the study (10)eat or drink too much during this trial, or who have a habit of eating out (11)treated cosmetic care (12)treated cosmetic care except for measuring sites, or hormonal therapy for one year (13)a facial, a wash-rag, lost hair on measuring sites for one month ago, or plans these actions (14)no habit of preventing sunburn (15)plan to have ultraviolet exposure within a month before the screening test (16)wash the body providing strong skin irritation (17)the skin chronic disease including atopic dermatitis (18)subjects who have the wound or inflammatory disease affecting the measuring skin (19)trouble by rough skin around a menstruates (20)subjects who work for anti-glycation foods related companies, or subjects who have family members working for such companies (21)employed on a pre-dawn shift or on night duty more than 2 times (22)planned to go overseas (23)possibilities for emerging allergy related to the study (24)judged as unsuitable for the study based on the results of clinical and physical examination on screening test (25)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 (26)planned to become pregnant after informed consent for the current study or are pregnant or lactating (27)judged as unsuitable for the study based on the results of lifestyle questionnaire (28)judged as unsuitable for the study by the investigator for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method