Healthy adults
Conditions
Interventions
Study food A will be ingested over a period of 15 minutes.
Study food B will be ingested over a period of 15 minutes.
Study food C will be ingested over a period of 15 minutes.
Placebo will be ingeste
Sponsors
IMEQRD Co., Ltd
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1.Aged 20 to under 35 at the time of informed consent 2.Japanese male 3.BMI of less than 25 kg/m2 4.Those who does not smoke (who have not been smoking for the last year) 5.Those who received sufficient explanation about the trial, volunteered to participate after understanding the purpose, and agree to participate in the trial with written consent
Exclusion criteria
Exclusion criteria: 1.Taking medication or Chinese medication (except for the drugs as needed) 2.Current or history of serious diseases such as heart, liver, kidney, gastrointestinal tract 3.Those who has pollinosis or allergic rhinitis (seasonal/perennial) 4.Under diet or exercise therapy under the supervision of a doctor 5.Those who regularly uses any commercially available drug and quasi-drug, food for specified health use, food with functional claims, or health food that affects autonomic nervous system, metabolism, and sleep (however, the person will be eligible if he/she can stop using it during the study period after provision of the informed consent) 6.Those whose eyes (e.g., exotropia, esotropia, eyelid ptosis) and eyelash shape are not suitable for pupillometry 7.Those who has a problem with wearing heart rate meters 8.Those who has dry eyes or a dry mouth, etc., that may disrupt pupillometry and saliva collection 9.Excessive consumption of alcohol (alcohol equivalent 60g or more / day) 10.Irregular diet, shift worker, night shift, irregular life rhythm 11.Those who has participated another clinical study within 1 month prior to provision of the informed consent or is currently participating in it, or will participate in it during the study period or within 4 weeks after the end of the study 12.Those who will be possibly under significant stress of any life event such as moving, changing his/her job, and separation from a close relative, within 3 months prior to provision of the informed consent, or will have such a life event during the study period 13.Those who has difficulty abstaining from alcohol starting from one day prior to the start of the study 14.Current or history of drug and/or food allergies 15.Those who is unable to drink alcohol constitutionally 16.Judged by the investigator to be unsuitable for participating in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Questionnaires to assess the psychological impact | — |
Secondary
| Measure | Time frame |
|---|---|
| Pupillary light reflex,Saliva test,Heart rate,Body surface temperature,Questionnaires | — |
Countries
Japan
Contacts
Public ContactHirokuni Kayama
IMEQRD Co., Ltd Planning and Sales Department
Outcome results
None listed