Healthy Adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1)Subjects who have received adequate explanation and understand the purpose and content of this study, volunteered freely, and are able to give their own written informed consent. (2)Healthy males and females from 20 to 65 years of age
Exclusion criteria
Exclusion criteria: (1)Subjects with allergies (drugs and test food-related foods) (2)Females who are pregnant, lactating, or willing to become pregnant during the study period (3)Subjects being treated for the following diseases Malignant tumore, renal failure, heart failure, myocardial infarction, cerebral infarction, immunodeficiency, collagen disease (4)Subjects with pacemakers or implantable cardioverter defibrillators (5)Smokers (average 21 cigarettes per day or more), regular users of alcohol (average daily net alcohol of 60g or more), or those with extremely irregular lifestyle habits. (6)Subjects taking prescription drugs that affect the study (7)Subjects who have participated in other clinical trials for 28 days before the date of informed consent or who are scheduled to participate during the study period. (8)Subjects who were deemed inappropriate for inclusion in the study by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Urinary UrotensinII levels Fingertip capillary clinical images Blood pressure and pulse | — |
Secondary
| Measure | Time frame |
|---|---|
| Various questionnaires, Blood oxygen saturation concentration, Comparison of the results of the previous year's and post-trial checkups, Optional persistent blood glucose measurement | — |
Countries
Japan
Contacts
SQL INC. CRC