lichen planus. lichen planus
Conditions
Interventions
Intervention 1: control group receive oral past with 0.1 % triamsinolon 4 times a day for 12 weeks. Intervention 2: intervention group receive oral past with 5% licorice 4 times a day for 12 weeks.
Treatment - Drugs
control group receive oral past with 0.1 % triamsinolon 4 times a day for 12 weeks
intervention group receive oral past with 5% licorice 4 times a day for 12 weeks
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 69 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: older than 18 years of age Exclusion criteria: patient with systemic disease; pregnancy; smoking; lesion with displasia; those who received treatment for OLP at least 1 month previous to beginning the study; lesion adjacent to amalgam filling
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Size of lesion. Timepoint: the first week second week first month third month. Method of measurement: with ruler and calpier. | — |
Secondary
| Measure | Time frame |
|---|---|
| Level of pain. Timepoint: the first week second week first month third month. Method of measurement: Visual analog scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFateme Arbabi-Kalati
Zahedan University of Medical Sciences
Outcome results
None listed