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Effect of Topical Mycophenolate, Zinc and Aloe vera in oral lichen planus ulcers

Phase 3
Conditions
Oral lichen planus.
oral lichen planus
l43.8
Registration Number
IRCT20200708048057N1
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
12
Inclusion Criteria

Age over 18 years
A patient who is diagnosed with lichen planus on pathological examination.
Willingness to participate in the study
Existence of a bilateral lesion

Exclusion Criteria

Pregnant and lactating women
Systemic use of corticosteroids
High blood pressure
Smokers
All items where topical corticosteroids are contraindicated, such as: uncontrolled diabetes, history of tuberculosis, gastric ulcer
Adjacent waste with amalgam filling
Systemic diseases

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Size of erythema and ulcer. Timepoint: 15 days after treatment. Method of measurement: dental micrometer (colis) .
Secondary Outcome Measures
NameTimeMethod
Pain and burning. Timepoint: 15 days after receiving the drug. Method of measurement: visual analog scale (VAS).
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