Effectiveness of micro-needling for oral lichen planus treatment

Phase 3

Recruiting

• Conditions: Oral Lichen Planus.; Lichen planus

• Registration Number: IRCT20231213060357N1
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Subjects aged 18 years or older
Subjects diagnosed with OLP based on the clinical or histopathological findings according to the newest diagnostic approach published by American Academy of Oral and Maxillofacial Pathology in ????
Subjects with bilateral symptomatic OLP lesions
Subjects who are willing to complete this clinical trial

Exclusion Criteria

Subjects with lesions that may be associated with lichenoid reactions
Subjects having a history of drug allergy
Subjects with a history of use of topical corticosteroids (in the past ? weeks) or systemic corticosteroids (in the past ? months) for oral lichen planus, other immunosuppressive treatments, retinoids, and anticoagulants
Subjects having oral candidiasis
Subjects with self-reported pregnancy or lactation

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain Level. Timepoint: At the beginning of the study (before the start of the intervention) and 14, 28, and 56 days after start. Method of measurement: Visual Analogue Scale.;Severity of the lesions. Timepoint: At the beginning of the study (before the start of the intervention) and 14, 28, and 56 days after start. Method of measurement: reticulation/erythema/ ulceration (REU) scoring system.