comparison the efficacy of bovine colostrum with topical triamcinolone acetonide 0/1%
Phase 2
- Conditions
- oral lichen planus.Lichen planus
- Registration Number
- IRCT201109197594N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Inclusion criteria: patients with erosive oral lichen planus; lack of effective systemic drugs for at least three months of oral lichen planus and lack of effective topical medications for at least a month of oral lichen planus.
Exclusion criteria: systemic disease; taking any medication lichenoied and consumption of any tobacco.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical extent of the lesion. Timepoint: Before Intervention- after two weeks Intervention -after four weeks Intervention. Method of measurement: Ruler (per square millimeter).
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: Before Intervention- after two weeks Intervention -after four weeks Intervention. Method of measurement: According to statements made by the patient (by scale VAS).;Burning sensation. Timepoint: Before Intervention- after two weeks Intervention -after four weeks Intervention. Method of measurement: According to statements made by the patient (by scale VAS).