IRCT20221018056229N1
Completed
Phase 3
Investigating the efficacy and safety of platelet rich plasma and topical clobetasol in treating hair loss of patients with lichen planopilaris in comparison to the patients who only use topical clobetasol
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Iran University of Medical Sciences
- Enrollment
- 22
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age: 18 years old and more
- •Definite and resistant hair loss due to LPP
- •The patient gives informed consent
- •The patient can participate in regular follow up meetings
- •The patient does not have serious internal disease
- •The patient does not have cutaneous disease in the site of treatment
Exclusion Criteria
- •History of any remedies taken in last month
- •Positive history of liver, kidney, pulmonary, cardiac, and intestinal disease and malignancies
- •Taking any medications for any disease which makes drug reactions possible
- •Accompanying of LPP with generalized lichen planus or erosive mucosal form
- •Other forms of noncicatricial or other forms of cicatricial alopecia except LPP
Outcomes
Primary Outcomes
Not specified
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