Effect of oral minoxidil in treatment of lichen planopilaris
Phase 2
Recruiting
- Conditions
- ichen planopilaris.Follicular Lichen PlanusL66.1
- Registration Number
- IRCT20220528055005N1
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
Newly diagnosed patients who have not yet received treatment.
Patients who have previously been treated and whose disease is still active according to clinical and dermoscopic criteria
Patients should have discontinued any previous systemic medication 1 month before entering the study and should not use any systemic or topical medication at the time of the study
Exclusion Criteria
pregnancy or breastfeeding
Leukocytes <3000
Platelets <100000
Hemoglobin <9
Liver enzymes more than 2 times the reference limit
Positive for viral hepatitis tests
History of cardiovascular disease and hypotension
History of arrhythmia (non-sinus rhythm on ECG)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ichen planopilaris activity index. Timepoint: Befor and after intervention. Method of measurement: Cheklist.;Standardized global photography. Timepoint: Befor and after intervention. Method of measurement: Based on scoring by two dermatologist.;Dermoscopy. Timepoint: Befor and after intervention. Method of measurement: Chcklist.
- Secondary Outcome Measures
Name Time Method