JPRN-UMIN000053673
Not yet recruiting
未知
Trial to Verify the Effects of the Primary Aroma of Test Food on the Autonomic Nervous System - Trial to Verify the Effects of the Primary Aroma of Test Food on the Autonomic Nervous System
CPCC Company Limited0 sites20 target enrollmentFebruary 21, 2024
ConditionsMale/female adults
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Male/female adults
- Sponsor
- CPCC Company Limited
- Enrollment
- 20
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\. Volunteers being poor at having a smell of any kind of tea. 2\. Volunteers falling into the habit of smoking (not less than half a year). 3\. Volunteers who have periodically used health\-specific / functional (e.g., gamma\-aminobutyric acid, L\-theanine)/ health foods including supplements, the trial results. 4\. Volunteers with incompatible eyeballs/eyelashes for pupillometry. 5\. Volunteers with any hindrances to a pupil measurement (e.g., dry eye). 6\. Volunteers having a subjective symptom of claustrophobia and nyctophobia. 7\. Volunteers being under some kind of continuous medical treatment. 8\. Volunteers with the condition of being over\-sensitiveness to cold, even during the summer season. 9\. Volunteers with nasal congestion and/or wrong judgement of fragrance. 10\. Volunteers with previous and/or current medical history of serious diseases in heart, liver, kidney and/or digestive organs. 11\. Volunteers with an external injury on their forehead or finger. 12\. Volunteers who are participating in the other clinical trials and/or who have participated in the other clinical trials within a month prior to the current trial and/or who are planning to participate in the other clinical trials. 13\. Volunteers with some kind of skin symptom, disease or disorder (e.g., atopic dermatitis). 14\. Pregnant, possibly pregnant, or lactating women. 15\. Volunteers deemed unsuitable for participation in the trial by the principal investigator or sub\-investigator.
Outcomes
Primary Outcomes
Not specified
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