IRCT20210513051276N1
Recruiting
Phase 2
Clinical trial of Comparison of the efficacy and safety of finasteride and hydroxy chloroquine on frontal fibrosing severity index in patients with frontal fibrosing alopecia
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Esfahan University of Medical Sciences
- Enrollment
- 30
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •New cases with FFA who have not yet received any medication.
- •Patients who have previously received systemic therapy and have not received systemic medication for at least the last three months and according to clinical and dermoscopic criteria, their disease is active.
- •Patients treated with topical medication and according to clinical and dermoscopic criteria, their disease is active
Exclusion Criteria
- •Pregnancy or lactation
- •History of hypersensivity due to hydroxychloroquine or finasteride
- •Patients with severe blood dyscrasia and liver dysfunction
- •Patients with retinopathy
- •Personal history or family history of breast cancer
Outcomes
Primary Outcomes
Not specified
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