FPHL
Conditions
Interventions
Subjects are divided into two groups (test article use group, non-intervention group) to evaluate the effects on hair.
Sponsors
Miyata Akinobu
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Female Pattern Hair Loss (FPHL) over 40 years old (including FAGA and alopecia areata) 2.Persons whose parietal condition corresponds to I-2 to II-1 on the Savin Female Density scale 3. When using the test equipment, test that you do not put or wear electronic products (including smartphones, chargers, music players, earphones, mobile games, etc.) within 1m from your body (including the next room across the wall). Those who can continue during the implementation period 4. Those who can promise not to wear metal objects (accessories, buttons, watches, hairpins, etc.) when using the test equipment. 5. Those who can promise not to wear chemical fiber clothing (polyester, nylon, vinyl, fleece, etc.) when using the test equipment (bedding such as 100% cotton or silk pajamas is acceptable) 6.Subjects who can use 100% cotton or linen sheets at bedtime during the test period. 7.Subjects who fully understood the participation in this research and gave written informed consent of their own free will.
Exclusion criteria
Exclusion criteria: 1.Subjects with symptoms of atopic dermatitis 2. Those who are receiving treatment, medication, or lifestyle guidance from a doctor 3. Severe cerebrovascular disease, heart disease, liver disease, renal disease, digestive system disease, infectious disease requiring notification, etc. suffering from 4. Those who use a pacemaker or defibrillator 5. Excessive smokers*1 and regular alcohol users*2 6.Subjects with significant abnormalities in blood pressure measurement and blood tests 7. Those who are pregnant or breast-feeding, or those planning to do so (including those who have just given birth) 8.Subjects who are receiving hormone replacement therapy 9.Subjects who plan to start new hair care (hair restorer, thinning hair treatment, hair beauty treatment, etc.) during the test period, or those who have started within the last 2 months 10. Subjects who have experience of aesthetic medicine on the test site, and who have hair thickening 11.Subjects who plan to change their lifestyle habits during the test period 12.Subjects who have participated in, or plan to participate in, other clinical trials that are affected by this study within one month prior to obtaining informed consent 13.In addition, those who are judged to be inappropriate by the principal investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hair diameter, crown evaluation, equipment measurement(number and density of hair) | — |
Secondary
| Measure | Time frame |
|---|---|
| subjective assessment | — |
Contacts
Public ContactTakeshi Kaneko
Japan Clinical Trial Association
Outcome results
None listed