Androgenetic alopecia. Androgenic alopecia
Conditions
Interventions
Intervention 1: Control group: Receive topical minoxidil foam 5% once a day. Intervention 2: Intervention group: Receiving topical minoxidil foam 5% once a day and injecting platelet-rich plasma 3 ses
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients willing to participate in the study Confirmatory diagnosis of androgenetic alopecia disease by two experts with skin and hair experience Women aged 18 to 60 years Moderate to severe hair loss
Exclusion criteria
Exclusion criteria: Patients suffering from other types of alopecia (such as alopecia areata, telogen effluvium, anagen effluvium and scarring alopecias) Patients with active psoriasis or active lichen planus due to the positive Köbner phenomenon in these diseases Any serious systemic disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increase density and thickness of hair. Timepoint: The beginning of the study and 6 months after the start of the study. Method of measurement: Trichogram, standard photography. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction score, doctor satisfaction score. Timepoint: The beginning of the study and 6 months after the start of the study. Method of measurement: A 10-point questionnaire is assigned for the patient's satisfaction, as well as a 10-point questionnaire that is completed by the doctor based on the comparison of the standard photography score and the comparison of the trichogram (checking the thickness and density of the hair). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactArezoo Refaghat
Esfahan University of Medical Sciences
Outcome results
None listed