healthy adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Persons with relatively high oxidized LDL/LDL cholesterol (2) Persons with relatively high LDL cholesterol/HDL cholesterol (LH ratio) (3) Persons with BMI 30 or lower (4) Persons who can visit designated facilities on scheduled visiting dates (5) Persons who fully understood the purpose and content of the trial and gave written consent
Exclusion criteria
Exclusion criteria: (1) Persons who are receiving any treatment at the time of participation in the trial (2) Pregnant women (including those who are potentially pregnant) or lactating women (3) Smokers (4) Persons who made a blood component donation or whole blood donation of 200 mL within 4 weeks prior to the trial food intake (5) Persons who made a whole blood donation of 400 mL within 16 weeks prior to the trial food intake (6) Persons who underwent blood drawing of over 1000 mL within 48 weeks prior to the trial food intake (7) Persons who are participating in other trials or studies (8) Persons who meet any of the following: 1) Persons with heart, liver or kidney diseases (including complications of other diseases) 2) Persons with medical history of circulatory diseases 3) Persons with diabetes mellitus 4) Persons currently receiving treatment for or with medical history of serious diseases such as cancer or asthma (9) Persons with history of major surgery in the site of gastrointestinal tract such as gastrectomy, gastroenterostomy, or intestinal resection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the amount of L/H ratio changes with placebo as a control | — |
Countries
Japan
Contacts
edihas Co., Ltd. Division of Clinical Trial Support