Adults in good health
Conditions
Interventions
Ingesting the jelly which contains test food, 3 sticks in a day, for 8 weeks.
Ingesting the jelly which does not contain test food, 3 sticks in a day, for 8 weeks.
Sponsors
CPCC Company Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Males and females aged 20 to 64 years old when obtaining informed consent. 2) Subjects whose body mass index (BMI) is and over 25.0kg/m2. 3) Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study.
Exclusion criteria
Exclusion criteria: 1) Subjects who are given continuous treatment by taking medicines. 2) Subjects who constantly use oral medicines, functional foods and/or supplements having a possibility of affecting test results. 3) Subjects who have previous and/or current medical history of serious disease in heart, liver, kidney and/or digestive trucks. 4) Pregnant or possibly pregnant females, or lactating females. 5) Subjects who excessive alcohol intake. 6) Subjects who have extremely irregular life rhythms, and subjects who have midnight work or irregular shift work. 7) Subjects who have previous medical history of drug and/or food allergy. 8) Subjects who are participating the other clinical tests of medicines or foods. Subjects who participated other clinical tests of medicines or foods within 4-weeks prior to the current study. 9) Subjects who donated over 200mL blood and/or blood components within a month to the current study. 10) Males who donated over 400mL blood within the last three months to the current study. 11) Females who donated over 400mL blood within the last four months to the current study. 12) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. 13) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. 14) Others who have been determined ineligible by principal investigator or sub-investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body weight, body mass index and body fat percentage. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intestinal microflora and blood lipid level. | — |
Countries
Japan
Contacts
Public ContactMasanori Numa
CPCC Company Limited Sales and Planning Department
Outcome results
None listed