An exploratory study on the effect of continuous intake of test food on vascular functions. -a single-arm, open-label trial- - An exploratory study on the effect of continuous intake of test food on vascular functions

IMEQRD Co., Ltd.0 sites10 target enrollmentFebruary 8, 2022

ConditionsHealthy adults

Overview

Phase: 未知
Intervention: Not specified
Conditions: Healthy adults
Sponsor: IMEQRD Co., Ltd.
Enrollment: 10
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

February 8, 2022

End Date

April 13, 2022

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

IMEQRD Co., Ltd.

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

•1\.Those who are currently undergoing treatment for any disease, or who receive medical treatment such as medical drugs or traditional Chinese medicines. However, medications used as needed will be allowed to join the trial. 2\.Those who have been receiving nutritional and exercise therapy under medical doctors. 3\.Those who have severe diseases or a history of severe diseases. 4\.Those who have severe anemia. 5\.Those who have currently been taking commercially available drugs, quasi\-drug products, foods, or supplements with any functional claims. However, Those who can discontinue taking these drugs/foods during the trial period will be allowed to join the trial. 6\.Those who have currently been utilizing any medical machines, such as warmth medical treatment, to improve fatigue, mental/physical stress, coldness, blood flow, blood pressure. However, Those who can discontinue using these machines during the trial period will be allowed to join the trial. 7\.Those who have a cold allergy, a drug allergy, or a food allergy. 8\.Those who smoke within one year before the trial. 9\.Those who drink more than 60 g alcohol/day. 10\.Women who have abnormal menstrual periods, or during menstruation on the day of visit. 11\.Those who donated blood more than 400 mL (men) or 200 mL (women) within three months before the trial. 12\.Those who are planning extremely change their lifestyle (such as diet, sleep, or exercise) during the study period. 13\.Those who work in shift and night shift. 14\.Those who are planning travel to foreign countries during the study period. 15\.Those who are currently pregnant or breastfeeding, or planning to pregnant during the study period. 16\.Those who joined other clinical trials from one month before the trial, or Those who have currently been joined other clinical trials. Also, Those who are planning to join other clinical trials during the trial. 17\.Those who are unsuitable for this study, that judged by the principal investigator.