Impact of oral lichen planus on oral health related quality of life
- Conditions
- Health Condition 1: 4- Health Condition 2: L439- Lichen planus, unspecified
- Registration Number
- CTRI/2023/08/055963
- Lead Sponsor
- SPPGIDMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 <br/ ><br>3weeks <br/ ><br>6weeks <br/ ><br>12weeks <br/ ><br>
- Secondary Outcome Measures
Name Time Method Demographic characterstics,and oral lichen planus related factors will be assesedTimepoint: baseline