None listed
Conditions
Interventions
100 mL of the test product is ingested at the time of testing.
Sponsors
KINJIRUSHI Co., Ltd
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1.Japanese healthy female subjects, between 20 years and 49 years old (inclusive) at the time of consent.
Exclusion criteria
Exclusion criteria: 1. Subjects who smoke tobacco. 2. Subjects who are alcoholic. 3. Subjects who have medical history that needs treatment or follow up. 4. Subjects who have some allergies of food or drug 5. Subjects who have plant allergy or allergic symptoms with aromatherapy. 6. Subjects who are taking medications that affect the autonomic nervous system. 7. Subjects who are olfactory disorder. 8. Subjects who participate in, at the time of initiation of this study, another test that interferes with this study or subjects who are scheduled to attend, during the tests, another test that interferes with this study. 9. Subjects who received chemical peel, laser treatment, light irradiation treatment, skin treatment such as injection, or surgery, or beauty therapy on the site of the skin test within 4 weeks by the start of the test. 10. Subjects who are judged as unsuitable by the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Salivary oxytocin 10 minutes before intervention and 10 minutes after intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Salivary cortisol 10 minutes before intervention and 1minutes after intervention Questionnaire | — |
Countries
Japan
Contacts
Public ContactDaisuke Aoyagi
KINJIRUSHI Co., Ltd R&D Division
Outcome results
None listed