Comparison of therapeutic effect of nigella sativa and corticosterioid in orabase on oral erosive atrophic lichen planus
Phase 1
- Conditions
- lichen planus.Lichen planus
- Registration Number
- IRCT20080907001222N2
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
patient with oral lichen planus
two oral lesions
maximum 3 cm diameter
Exclusion Criteria
systemic compromised patients
lesion of posterior palate and oral floor
pregnant and breast feeding patients
children under 8 years old
patients using immunosuppressant drugs
lichenoid reaction lesions
nigella sativa hypersensitivity
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of oral lesion. Timepoint: weekly up to one month. Method of measurement: tongprasom scale.
- Secondary Outcome Measures
Name Time Method Burning sensation. Timepoint: Pain and burning sensation will be measured before intervention and then weekly for one month. Method of measurement: Visual Analogue Scale.