Healthy Adults
Conditions
Interventions
4 weeks).
Sponsors
Healthcare Systems Co., Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document. 2. Japanese males and postmenopausal females aged 50 - 64years, at the time of obtaining consent to participate. 3. Persons whose BMI is more than 23.0 kg/m2 and less than 30.0 kg/m2
Exclusion criteria
Exclusion criteria: 1.Persons who have chronic diseases are currently suffering from any disease, are undergoing treatment, or have a history of any disease. 2.Persons who have a habit of taking medication for the purpose of disease treatment in the past month (except for a history of taking medication for headache, common cold, etc.). Persons who regularly use medicines or quasi-drugs for purposes other than the treatment of diseases. 3.Persons who are allergic to the test food, may have allergic symptoms to other foods or medicines. 4.Persons who regularly take a large amount of the test food, cinnamon, and rooibos tea. 5.Persons who regularly use medicines or health functional foods (food for specified health use, food with functional claims and nutrient functional food) that may affect the capillary morphology. 6.Persons with severe anemia symptoms. 7.Persons with dental or oral problems (periodontal disease, mouth ulcers, etc.) that cause bleeding. 8.Persons whose daily alcohol consumption exceeds 20 g of pure alcohol equivalent per day per day. 9.Persons whose lifestyle may change during the examination period (e.g., night work, extended travel, exercise, etc.). 10.Persons who habitually engage in strenuous exercise such as running, marathons, volleyball. 11.Persons who are unable to discontinue nail polish or fake fingernails during the examination period. 12.Persons who have donated over 200 mL of blood in the past month or over 400 mL within the past 3 months. 13.Persons who have experienced feeling unwell or deterioration of physical condition due to blood collection in the past. 14.Persons who have participated in other tests within the first month before the start of the test, or those who intend to participate in another exam after consenting to this exam. 15.Persons who were judged as inappropriate for study participants by the principal investigator. 16.Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Angiopoietin2 in blood Status of capillary | — |
Countries
Japan
Contacts
Public ContactSuzuka Oyama
Healthcare Systems Co., Ltd. Clinical Research Department
Outcome results
None listed