Healthy subjects
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Men and women aged 20 to 50 at the time of consent 2)Those who feel that they consume too little vegetables in their daily lives 3)Subjects who have fully understood the purpose of participating in this clinical study and have given their voluntary written consent
Exclusion criteria
Exclusion criteria: 1)with following diseases Type2 diabetes,glucose tolerance,dyslipidemia,hypertension(exclude grade1 hypertension),hyperuricemia,gout,myocardial infarction,angina pectoris,cerebral thrombosis,transient ischemic attack,fatty liver(nonalcoholic fatty liver),menstrual abnormalities,pregnancy complications(pregnant with hypertension,gestational diabetes),sleep apnea syndrome,obesity hypoventilation syndrome, osteoarthritis(knee,hip),spondylosis,low back pain,obesity-related kidney disease,other chronic diseases(digestive,cardiac,liver,kidney,neurological,stroke,rheumatism,etc.) 2)who history or complications of malignancy 3)who family history of diabetes or glucose tolerance 4)who treat by drug,device,rehabilitation,etc.,regardless of seasonal,chronic,sudden illness at screening 5)who medical history in 3months 6)who BMI is less than 18.5 and over 25kg/m2 7)who surgery in past 8)with food allergy or sensitive or specific constitutions 9)who on drug treat 10)who experienced feel unwell or worse physical condition by blood drawn past 11)who donated 200mL within 4weeks or component donated within 2weeks prior to intake 12)Women who donated 400mL within 16weeks prior to intake 13)Men who donated 400mL within 12weeks prior to intake 14)who taking Over-the-counter drug,supplements,or foods for specified health uses 15)who wish to pregnant during the study 16)who breastfeed,pregnant and plan to pregnant 17)judged by the principal to require treat for mental illness 18)who smoke or alcohol excessively 19)who nightwork,cannot take regular off,irregular lifestyles 20)who likely to experience major changes in living environment(home,work,etc.)during the study(moving,job transfer,longtravel,etc.)or in their eating or exercise habits 21)who currently participating other study,participated within 4weeks of WEB screening,or scheduled to participate other study during the study 22)who cannot comply management matters during the study 23)judged inappropriate for the study by principal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)Postprandial blood glucose level 2)Blood insulin levels 3)HbA1c | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)Serum electrolyte concentrations (Na, K, Cl-) 2)BMI | — |
Countries
Japan
Contacts
Macromill, Inc. Clinical Research Unit, Life Science Division