alopecia areata. Alopecia areata
Conditions
Interventions
Intervention 1: Intervention group1: 30 patients with alopecia areata who are receiving topical diphencyprone with new regimen. Intervention 2: Intervention group 2: 30 patients with alopecia areata
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with alopecia areata Possibility of regular visit for the patient Hair loss more then 50 % The age of the patient greater than 18 years old
Exclusion criteria
Exclusion criteria: Pregnancy and lactation Persistent totalis or universalis areata alopecia from infancy Prominent androgenetic alopecia No response to diphencyprone test Patients with hematologic dysplasia receiving systemic immunosuppressive therapy during recent 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Terminal hair regrowth rate with topical diphencyprone with old regimen in comparison to new regimen in patients with alopecia areata, based of SALT score. Timepoint: before intervention and 3 and 6 months after intervention. Method of measurement: Severity of Alopecia Tool Score. | — |
Secondary
| Measure | Time frame |
|---|---|
| Rate of change in Severity of Alopecia Tool score than the base value, after intervention and at the end of course of treatment. Timepoint: 3 and 6 months after treatment. Method of measurement: Severity of Alopecia Tool score. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDoctor Alaa Al Bazzal
Tehran University of Medical Sciences
Outcome results
None listed