Platelet Rich Plasma for Frontal Fibrosing Alopecia

Inclusion Criteria

• •Males and females, ages 18 and older
• •Diagnosed by a board-certified dermatologist with frontal fibrosing alopecia
• •Scalp biopsy consistent with frontal fibrosing alopecia diagnosis
• •Willing to use Head and Shoulders shampoo for the scalp while in study
• •Willing to abstain from over the counter and prescription hair/scalp products other than those supplied in the study
• •Willing to abstain from the use of non-steroidal anti-inflammatory medications, aspirin, St, John's Wart, and high doses of Vitamin E supplementation for 4 weeks
• •Subjects must be capable of giving informed consent
• •Stated willingness to comply with all study procedures and be available for the duration of the study
• •For women with reproductive potential, a willingness to use methods of contraception that will prevent the subject from becoming pregnant during the study. Adequate contraception methods include hormonal methods used for two or more menstrual cycles before screening (eg. oral contraceptive pills, contraceptive patch, or contraceptive vaginal ring), barrier methods (eg, contraceptive sponge, diaphragm in conjunction with contraceptive foam or jelly, or condom in conjunction with contraceptive foam or jelly), intrauterine methods (IUD), sterilization (eg, tubal ligation or a monogamous relationship with a vasectomized partner) and abstinence