Health Condition 1: 4- Health Condition 2: L439- Lichen planus, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Aged 18 years or older 2)Clinically and histopathologically proven OLP based upon modified WHO diagnostic criteria (van der Meij & van der Waal, 2003)able to understand and complete questionnaires in loco regional language 3)Agree to participate and provide written informed consent
Exclusion criteria
Exclusion criteria: 1)Evidence of proven hypersensitivity to dental materials 2)Evidence of oral lichenoid lesions associated with graft-versus-host disease and systemic lupus erythematosus 3)Having coexisting chronic neuropathic orofacial pain, 4)Severe systemic disease and/or some psychiatric conditions 5)Patients with painful symptomatology, and subjects treated with oral and topical corticosteroids or regularly treated with anxiolytic, antidepressants, anticonvulsants or psychotrophic drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome by using patient reported outcome measure to see the changes in the clinical score and actual, physical ,functional,and emotional well being of the patients being treated over a period of time.Timepoint: Baseline 3weeks 6weeks 12weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Demographic characterstics,and oral lichen planus related factors will be assesedTimepoint: baseline | — |
Countries
India
Contacts
Sardar patel post graduate institute of dental and medical sciences