Healthy subjects
Conditions
Interventions
Single intake of test food after conducting Uchida-Kraepelin test on the test day
Single intake of test food after conducting Uchida-Kraepelin test on the test day
Sponsors
HUMA R&D CORP
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1.Japanese male aged 20 years or older and younger than 50 years at the time of the informed consent. 2.Subjects without smoking habits 3.Subjects who can take alcohol 4.Subject who has understood the purpose of the study, and agreed to participate it by signing the written informed consent.
Exclusion criteria
Exclusion criteria: 1.Subject with BMI>=25kg/m2 2.Subject who have an onset or history of eye disease(Excludes mild illnesses such as infectious diseases) 3.Person with eyelid droop 4.Subject who have moved or changed their jobs within the last 3 months, separated from their close relatives, etc., and are likely to have great 5.Subject who is taking medication or under medical treatment because of some serious illness. 6.Subject who is under exercise therapy or dietetic therapy. 7.Subject who has an allergy for test food. 8.Subject who has or had a history of either medicine or alcohol dependence syndrome. 9.Subject who has or had a history of mental illness (depression) or sleep disturbance. 10.Subject who is on a night-shift or is a shift worker. 11.Subject whose lifestyle is extremely irregular. 12.Subject who has an unbalanced diet. 13.Subject who is disease or history such severe diseases such as brain disease, malignant tumor, immune disease, diabetes, liver disease (hepatitis), kidney disease, heart disease, thyroid disease, adrenal disease, other metabolic diseases person. 14.Subject who uses health foods ,supplements, and medicines that are thought to affect autonomic nerves, sleep, and stress 15.Subject who has participated in other clinical studies within the past 3 months from the day of the consent acquisition or who is planning to participate in other clinical studies during the current study. 16.Subject who can't keep the daily records. 17.Subject who is considered as an inappropriate candidate by the doctor in charge.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Electronic pupillometer measurement data | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate sensor measurement data,questionnaire | — |
Countries
Japan
Contacts
Public ContactDaisuke Ochitani
HUMA R&D CORP Clinical Development Division
Outcome results
None listed