A confirmation study of anti-obesity effect by test food intake. - Confirmation of anti-obesity effect of the test food.

CPCC Company Limited0 sites24 target enrollmentNovember 22, 2016

ConditionsAdults in good health

Overview

Phase: 未知
Intervention: Not specified
Conditions: Adults in good health
Sponsor: CPCC Company Limited
Enrollment: 24
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

November 22, 2016

End Date

TBD

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

CPCC Company Limited

Eligibility Criteria

Inclusion Criteria

Not provided

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.