Platelet Rich Plasma Versus Minoxidil Foam for Treatment of Androgenic Alopecia in Women

Inclusion Criteria: 1. Only female patients are eligible 2. Patients must be 18 years of age or older 3. Patients must have Androgenic Alopecia Grade I-II by Ludwig Classification 4. Patients must have been on stable birth control if premenopausal. 5. Patients are able and willing to provide written informed consent after the nature of the study is fully explained Exclusion Criteria: 1. Patients with clinically abnormal hematology, serum chemistry, or screening laboratory results as reviewed by the Principal Investigator 2. Patients who have undergone topical and systemic therapies for hair loss 3 months prior to the procedure 3. Patients who have used any cosmetic product meant to address hair loss 3 months prior to enrollment 4. Patients taking anti-rheumatic disease medication (including methotrexate or other anti-metabolites) within the 3 months prior to study entry. 5. Patients previously having undergone hair transplant surgery prior to study entry 6. Patients who are pregnant or currently breast-feeding children as Rogaine for Women is contra indicated for these women 7. Patients who have taken spironolactone in the 3 months prior to study participation 8. Patients with systemic, rheumatic or inflammatory disease or who are immunosuppressed 9. Patients with ongoing infectious disease, including HIV and hepatitis 10. Patients with clinically significant cardiovascular, renal, hepatic, endocrine disease, cancer, or diabetes 11. Patients participating in a study of an experimental drug or medical device within 30 days of study entry 12. Patients with history of platelet disorders, bone marrow aplasia, sepsis, or cancer in the last 5 years. 13. Patients taking antiaggregating therapy 14. Patients on anticoagulant therapy 15. Patients with tendency to keloid formation 16. Patients with uncompensated diabetes 17. Patients with active skin disease or skin infection at intended treatment areas