The comparison of two regimens of diphencyprone in alopecia areata patients.
Phase 3
Recruiting
- Conditions
- alopecia areata.Alopecia areata
- Registration Number
- IRCT20141209020250N5
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.