Frontal Fibrosing Alopecia. Lichen planopilaris
Conditions
Interventions
in the first group the first 2 weeks of intervention includes local daily clobetasol for 5 days then local tacrolimus daily for 2 days, at the end of second week the patient will apply local daily tac
Treatment - Drugs
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Inclusion criteria: patients with clinicopathologically proven FFA, older than 18 years Exclusion criteria: 1. pregnancy 2. inability to participate or follow the trial 3. severe hypertriglyceridemia 4. liver enzyme disturbance 5. consumption of immunosuppressant or another kind of LLP or FFA therapies during recent 3 months
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frontal Fibrosing Alopecia Severity Index (FFASI). Timepoint: before trial and in 2, 4, and 6 months later. Method of measurement: Questionaire.;Hair amount and density. Timepoint: before trial and in 2, 4, and 6 months later. Method of measurement: Fotofinder.;Clinical presentations (itching and irritation). Timepoint: before trial and in 2, 4, and 6 months later. Method of measurement: Patient asking. | — |
Secondary
| Measure | Time frame |
|---|---|
| Perifollicular scaling. Timepoint: before trial and in 2, 4, and 6 months later. Method of measurement: Trichoscope.;Perifulicular erythema. Timepoint: before trial and in 2, 4, and 6 months later. Method of measurement: Trichoscope. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Mohammad Amini
Tehran University of Medical Sciences
Outcome results
None listed