Hair Regrowth Effect of Non-contact Focused Ultrasound Irradiation in Patients with Female Pattern Alopecia

Yoshihiro Yasuda0 个研究点目标入组 50 人开始时间: 2022年10月21日最近更新: 2023年10月17日

适应症

试验速览

暂无简介。

•1. Japanese female subjects who are between 20 and 50 years of age at the time of obtaining written conse
•nt to participate in the study and who have an understanding of the study
•2. have FPHL (Savin classification: II-III, Advanced)
•3. who are able to shave the evaluation site and come to the clinic for the procedure
•4. who can come to the hospital on the designated examination and treatment days and undergo the examination
•5. who are basically engaged in indoor work
•6. who have explained about the study using the consent document and obtained consent

•1. those with anemia, thyroid disease, collagen disease, polycystic ovaries, hyperprolactinemia, or other conditions that cause symptoms of hair loss
•2. those who consume excessive amounts of alcohol
•3. those whose lifestyle may change during the examination period (e.g., working at night, traveling for long periods of time)
•4. who have participated in other clinical trials or clinical studies from the past 6 months to the present
•5. who are currently undergoing treatment for FPHL (medication, hair transplantation, etc.)
•6. who have been determined to have alopecia due to postpartum
•7. who have used drugs such as RiUP for the treatment of female pattern baldness within the past 3 months
•8. those who have skin conditions such as skin allergies, atopic dermatitis, seborrheic dermatitis, etc. on the scalp
•9. Women who are pregnant or may become pregnant, or who wish to become pregnant during the study period
•10. any other person whom the principal investigator or subinvestigator determines to be inappropriate to participate in this study.

发起方

Yoshihiro Yasuda