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The effect of triamcinolone and Q10 coenzyme in the treatment of oral lichen planus

Phase 3
Recruiting
Conditions
oral lichen planus.
Lichen planus
Registration Number
IRCT20201127049502N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
18
Inclusion Criteria

Patients with symptomatic oral lichen planus (erosive or atrophic form) who have a sense of burning or pain.
The diagnosis is clinical (Wickham striae or papules) and in cases in which a definitive diagnosis of the lesion is difficult, a histopathological evaluation will be used.
The patient should not have used topical corticosteroid treatments in the last two weeks or systemic corticosteroids in the last month.
The patient should not have used analgesics and anesthetics.

Exclusion Criteria

Patients with lichenoid lesions caused by medication or dental materials
Pregnant or lactating patients
Patients with other lesions such as leukoplakia and systemic lupus in conjunction with lichen planus
History of malignancy
Non-cooperative patients and patients who do not use drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity and size of the lesions based on REU index. Timepoint: baseline(day0), day15, day30. Method of measurement: Graded tongue blade.;Amount of healing based on E?cacy Index. Timepoint: baseline(day0), day15, day30. Method of measurement: formula.;Severity of burning sensation based on VAS Index. Timepoint: baseline(day0), day15, day30. Method of measurement: Scoring by the patient.
Secondary Outcome Measures
NameTimeMethod
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