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The effect of postbiotic mouthwash on oral ulcerative lichen planus lesions

Phase 3
Recruiting
Conditions
oral lichen planus.
Lichen planus
Registration Number
IRCT20240122060773N1
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Patients suffering from ulcerative or erosive oral lichen planus based on the diagnosis of an oral disease expert in the clinical view and its confirmation by an oral pathologist from the biopsied tissue.
Patients with pain higher than 2 on the visual analog scale during the initial clinical examination
Age range from 18 to 60 years at the time of signing the informed consent
At least one erosive mucosal tissue larger than 1 cm
Consent to participate in the study

Exclusion Criteria

Patients with gastrointestinal ulcers
Patients with uncontrollable and severe medical conditions
Patients with dementia, mental disorders or alcohol addiction
Pregnancy and breastfeeding
Patients who have a history of taking immunosuppressive drugs in the last 4 weeks.
Patients with dysplastic lesions

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intensity of pain. Timepoint: One week, two weeks and four weeks. Method of measurement: Visual Analogue Scale.;The size of oral ulcers. Timepoint: One week, two weeks and four weeks. Method of measurement: periodontal probe.;Recurrence rate. Timepoint: One week, two weeks and four weeks. Method of measurement: Therapist observation and patient report - periodontal probe and visual analog scale test.
Secondary Outcome Measures
NameTimeMethod
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