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Investigating the efficacy and safety of platelet rich plasma in treating hair loss of patients with lichen planopilaris

Phase 3
Conditions
Scalp hair lichen planopilaris.
Other lichen planus
L43.8
Registration Number
IRCT20221018056229N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
22
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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The amount of scalp pruritus based on LPPI. Timepoint: Investigating of scalp hair situation with using dermatoscope, at the first visit, at 1 month and 2 months and then 6 months after the first visit. Method of measurement: Dermatoscopy with dermatoscope.;The amount of scalp erythema based on LPPI. Timepoint: Investigating of scalp hair situation with using dermatoscope, at the first visit, at 1 month and 2 months and then 6 months after the first visit. Method of measurement: Dermatoscopy with dermatoscope.;The amount of scalp scaling based on LPPI. Timepoint: Investigating of scalp hair situation with using dermatoscope, at the first visit, at 1 month and 2 months and then 6 months after the first visit. Method of measurement: Dermatoscopy with dermatoscope.
Secondary Outcome Measures
NameTimeMethod
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