Healthy female adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Healthy female subjects ranging in age from 20 to 64. (2) Subjects who can give informed consent to participate in this research after being provided with an explanation of the protocol detail.
Exclusion criteria
Exclusion criteria: (1) Subjects falling into the habit of smoking. (2) Subjects with some kind of continuous medical treatment, at the moment of giving informed consent to participate in this research. (3) Subjects who have undergone some kind of medical treatment/application within the last month into this research (except taking in some cold remedies, but curing pollinosis). (4) Subjects having present/previous medical history of serious diseases in liver, kidney, heart, lung, and/or blood. (5) Pregnant, possibly pregnant, or lactating women. (6) Subjects with some kind of skin symptom, disease or disorder, just like atopic dermatitis. (7) Subjects having experience of some kind of skin-related trouble, because of putting a surgical tape on their facial part and/or region of chest. (8) Subjects who have undergone some kind of surgical treatment for their head, including neck/facial/parietal operations, within six months into this trial. (9) Subjects who are now under the other clinical trials with some kind of medicine/food, or have participated in similar tests within a month after those. (10) Others who have been determined as ineligible for participation, judging from the investigator's opinions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Brain waves 2. Heart rate variability | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Visual Analog Scale (VAS)- questionnaire scores 2. Oxytocin in saliva | — |
Countries
Japan
Contacts
CPCC Company Limited Planning & Sales Department