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The effect of platelet-rich plasma on oral lichen planus

Phase 1
Conditions
Oral lichen planus.
Lichen planus
Registration Number
IRCT20120101008585N10
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
15
Inclusion Criteria

The patients with atrophic or erosive oral lichen planus
The patients with histopathology and clinically conformed lichen planus
The patients who will be referred to Oral and Maxillofacial Disease Department of Shiraz Dental School

Exclusion Criteria

The patients with history of other inflammatory diseases pregnant women
The patients with history of malignancies or even dysplastic lesionsThe patients who have received treatment for oral lichen planus lesions since a previous month
pregnant women

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Days 0, 14, 30, 60. Method of measurement: Visual analogue scale.;Size. Timepoint: Days 0, 14, 30, 60. Method of measurement: Scaled tongue blade(mm).
Secondary Outcome Measures
NameTimeMethod
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