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Examination of the effect of test food intake on improving vascular function in healthy adults-Randomized, double-blind, placebo-controlled, parallel-group study

Not Applicable
Conditions
one (Healthy adults)
Registration Number
JPRN-UMIN000049050
Lead Sponsor
Kirin Holdings Company, Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
66
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who have been diagnosed with heart disease, liver disease, kidney disease, respiratory disease, endocrine disease, metabolic disease, or a history of these diseases (2) Subjects who have the disease under treatment (3) Subjects who regularly use supplements, health food (including foods for specified health use / foods with functional claims) during the test period (4) Subjects who have currently been taking medicines, supplements / health foods or cosmetics with any functional claims such as L-citrulline, L-arginine, L-ornithine, procyanidins, bonito elastin, linolenic acid, DHA, EPA, CoQ10, nattokinase, lutein, blueberries, cassis, vitamin E, ginkgo biloba extract, melilot, polyphenols (hesperidin, flavangenol, pycnogenol etc.) (5) Subjects who have currently been taking medicines, supplements / health foods or cosmetics for the purpose of improving blood flow and blood pressure in addition to the ingredients listed in (4) (6) Subjects who take part in another clinical study during the study, or who have participated as subjects in another clinical trials within the past 3 months (7) Subjects who are excessively take alcohol (expressed in an amount of alcohol: over 20g/day) (8) Subjects who have a smoking habit (those who smoke daily or occasionally in the last 3 months) (9) Subjects who conduct hormone replacement therapy in the 3 months. (10) Asthma patients (11) Subjects who have severe anemia (12) Subjects who have multiple irregularities in their lives during the research period due to day / night shift work or night work, or those who are engaged in physical labor such as transporting heavy objects. (13) Subjects who have been pregnant , or have a plan to breast feed during the study period (14) Subjects who are judged by the investigator to be inappropriate as subjects based on the test results at the time of screening (15) Subjects deemed unsuitable by the investigator for other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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