Comparison of different treatment options in oral lichen planus and oral submucous fibrosis
Phase 4
Completed
- Conditions
- Health Condition 1: null- Oral lichen planus
- Registration Number
- CTRI/2018/04/013147
- Lead Sponsor
- Maulana Azad Institute of Dental Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
Clinically and histopathologically proven cases of oral lichen planus and oral submucous fibrosis.
Exclusion Criteria
1. Patients not willing to participate
2. Undergoing alternative treatment for the same condition.
3. Severe uncontrolled systemic disease and pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. For oral lichen planus <br/ ><br>Evaluation of site score, severity score and activity score based on Escudier scale and burning sensation using VAS score <br/ ><br>2. For oral submucous fibrosis <br/ ><br>Mouth opening, tongue protrusion, cheek flexibility and VAS scoreTimepoint: At the time of first visit and every 4 weeks till 9 months
- Secondary Outcome Measures
Name Time Method Reporting of any malignant transformation over a period of 9 monthsTimepoint: individuals will be assessed every 4 weeks and in case of any suspicion, biopsy will be done