Safety test of the aromatherapy using the essential oil which was extracted from Abies sachalinensis
Not Applicable
- Conditions
- Healthy adults (In the future Alzheimer's disease)
- Registration Number
- JPRN-UMIN000020034
- Lead Sponsor
- Department of Biological Regulation, School of Health Science, Faculty of Medicine, Tottori University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1) Subjects who have a serious allergic disease 2) Subjects who are diagnosed olfactory disturbance 3) Subjects who have a serious heart disease 4) Subjects who have the past of epilepsy 5) Pregnant women or the subjects who may become pregnant 6) Subjects who are assessed by the principal investigator due to other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The results of blood tests and blood pressure test after four weeks
- Secondary Outcome Measures
Name Time Method The results of Touch Panel-type Dementia Assessment Scale (TDAS) and questionnaire after four weeks