Menopause(hot flashes)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Yokohama Port Side Female General Clinic Patient, Zushi Medicine Clinic Patient Yokohama City University staff, Yokohama City University affiliated hospital staff, Yokohama City University attached citizen general medical center staff
Exclusion criteria
Exclusion criteria: (1)HRT was enforced within 30 days before the start of the study. (Women 's medicine and supplements of Chinese herbal medicine and general medicine not containing estrogen preparation are acceptable.) (2)Allergy against essential oil used (3)There is skin disease (4)HRT and Surgical menopause treatment is in effect (5)Menopausal symptom interview sheet (Document IV) There are other diseases that fall under Q4 (2) - (16) (not limited to the presence or absence of treatment) (6)Participate in other exams within 30 days before the exam (7)In addition, patients judged unsuitable as subjects by doctor's judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the following items 21 days after the start of intervention. Symptom change of hot flashes: Evaluation of change occurring in the number of times and degree of hot flash by hot flash memory. Estrogenic activity: For each test, about 20 ml of urine is collected on the first day and the last day of the test and E2, FSH, LH are chromatographed, and the difference in hormone levels occurring between the intervention group and the control group is evaluated. Physical symptom change of menopausal disorder: Relative evaluation in somatic symptom change of 14 items described in hot flash memory | — |
Countries
Japan
Contacts
Yokohama City University Department of Biological Science and Nursing, Graduate School of Medicine