Healthy person
Conditions
Interventions
Test food(Intake priod:12 weeks)
Placebo(Intake priod:12 weeks)
Sponsors
FANCL Corporation
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Healthy male and female aged 20 to 64 years at the time of informed consent. 2)LDL cholesterol levels>=120 mg/dl and <160 mg/dl. 3)Subjects who agree to participate in the study on one's own will.
Exclusion criteria
Exclusion criteria: 1)Subjects who are suffering or suffered from serious disease such as kidney, liver, circulatory system, malignant neoplasm, mental, dementing disorder. 2)Subjects who are suffering or suffered from alcohol abuse disorder. 3)Subjects who are receiving medication. 4)Subjects who have allergy related to the study foods. 5)Subjects who cannot stop using health foods(supplements, foods for specified health use, displayed functional foods), quasi-drugs, medicines that decrease LDL cholesterol while study term. 6)Subjects who have participated in other clinical studies within the past 3 months prior to obtaining of the informed consent, or who are planning to participate in other clinical studies during the present study. 7)Subjects who are pregnant or breast-feeding. 8)Subject who cannot stop drinking alcohol from 2 days before screening inspection and each examination. 9)Subject who are shift workers, or late night workers. 10)Subjects who have been diagnosed with familial hyperlipidemia. 11)Subjects who are judged as unsuitable for the study by the doctor and the investigator in charge for other reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| blood LDL cholesterol levels | — |
Secondary
| Measure | Time frame |
|---|---|
| blood total cholesterol levels blood non-HDL cholesterol levels | — |
Countries
Japan
Contacts
Public ContactEiji Yoshikawa
KSO Corporation Sales department
Outcome results
None listed