Healthy adult Female
Conditions
Interventions
Daily use of certain cosmetics and once every two weeks, on one side of the face, a treatment with a medical RF beauty device
The other side of the face is not treated with medical RF beauty device an
Sponsors
Japan Clinical Trial Association
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Subjects who are concerned about sagging, swelling, and lines on the face. 2. Subjects who can use facial/beauty equipment on their face 3. Subjects who are tolerant to heat/electrical stimulation 4. No significant weight fluctuation of more than plus minus 3 kg from 4 weeks prior to the start of the study and able to maintain the weight from the start of the study to the end of the study. 5. Subjects who can agree not to change the cosmetics (skin care and make-up) used from 4 weeks prior to the start of the study to the end of the study. 6. The applicant agrees not to undergo any facial treatment or care at an esthetic or medical institution from the start date of the examination until the end of the examination.
Exclusion criteria
Exclusion criteria: 1. Subjects with serious underlying diseases (diabetes, dyslipidemia, cardiovascular disease, osteoporosis, autoimmune disease, etc.) 2. Subjects with chronic skin diseases such as atopic dermatitis 3. Subjects with a history of other serious diseases 4. Currently undergoing hospitalization, medication, or treatment for any disease. 5. Subjects have sensitive skin. 6. Subjects, lactating, or possibly pregnant. 7. Subjects who have undergone immunosuppression or other procedures within the past 3 months. 8. Subjects who have gold threads implanted or are taking or have a history of taking gold preparations (Siozol, Glelease, Rizasto, Ridora, etc.) 9. Subjects who are using a pacemaker or implantable cardioverter defibrillator 10. Subjects who have scars, warts, pimples, art makeup, burns, etc. on the face that may affect the evaluation measurement. 11. Subjects who have any experience of cosmetic or other medical treatment that may affect the subject area (including hyaluronic acid injections, Botox, etc.) 12. Subjects who have more than 5 metallic objects (bolts, silver teeth, etc.) in the treatment of the upper jaw. 13. Subjects who are undergoing dental treatment (braces, implants, etc.) 14. Subjects who may have allergic reactions to test product ingredients. 15. Claustrophobia 16. Subjects who have a smoking habit. 17. Subjects who have difficulty in maintaining their lifestyle (diet, exercise, sleep, skin care, etc.) 18. Subjects who drink excessively (e.g., more than 500 ml of beer, 1 cup (180 ml) of sake, 2 glasses (200 ml) of wine)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of devices that measure, Physician Evaluation (Before use / 2 weeks later / 4 weeks later / 8 weeks later) | — |
Countries
Japan
Contacts
Public ContactTakeshi Kaneko
Japan Clinical Trial Association N.A.
Outcome results
None listed