A examination test of effects on blood pressure by consumption of the test food - A examination test of effects on blood pressure by consumption of the test food

CPCC Company Limited0 sites72 target enrollmentApril 20, 2020

ConditionsHealthy adults

Overview

Phase: N/A
Intervention: Not specified
Conditions: Healthy adults
Sponsor: CPCC Company Limited
Enrollment: 72
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

April 20, 2020

End Date

December 13, 2019

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 have a disease or who are given continuous treatment by taking medicines. (2\) Subjects who plan to start treatment by taking medicines such as pollen allergy during the test term. (3\) Subjects who constantly use oral medicines, functional foods, health foods and/or supplements having a possibility of affecting blood pressure. (4\) Smokers (5\) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period. (6\) Subjects who have previous and/or current medical history of serious disease (e.g., heart, liver, kidney, digestive organ). (7\) Subjects who excessive alcohol intake. (8\) Subjects who have extremely irregular dining habits, and subjects who have irregular life rhythm such as shift work or midnight work. (9\) Subjects who have previous medical history of allergy for drugs, foods (especially for melon and apple), ribgrass pollen and/or lawn pollen. (10\) Subjects who are weak to acidic taste (11\) Subjects who are participating the other clinical tests. Subjects who participated within 4\-weeks prior to the current study and/or who plan to participate the other clinical tests. (12\) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. (13\) Males who donated over 400mL blood within the last three months to the current study. (14\) Females who donated over 400mL blood within the last four months to the current study. (15\) Males who will be collected over 1200mL blood, when the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. (16\) Females who will be collected over 800mL blood, when the sampling amounts within the last twelve months are adding to the planned sampling amounts of this study. (17\) Others who have been determined ineligible by principal investigator or sub\-investigator.