The effect of lycopene in the treatment of oral lichen planus
Phase 3
- Conditions
- oral lichen planus.Other lichen planus
- Registration Number
- IRCT201601113133N8
- Lead Sponsor
- Vice chancellor for research,Zahedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 2
Inclusion Criteria
Diagnostic criteria is clinical and histopathological view of the lesions.
Exclusion criteria: patients with systemic disease, skin lichen planus, drug user, pregnant wemen, smokers, patients with dysplastic lesions and lesions close to restorations and also patients receiving treatment for oral lesions was than a month ago.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in size of the lesion. Timepoint: Before starting treatment, every week for 12 weeks after starting treatment. Method of measurement: In each follow up session size of the lesion will be measured by caliper.
- Secondary Outcome Measures
Name Time Method Reduced pain of the lesion. Timepoint: Before starting treatment, every week for 12 weeks after starting treatment. Method of measurement: Use of Visual Analoge Scale (VAS) from 0- 10, 0: no pain sensation and 10: severe pain sensation.