Oral lichen planus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subjects are enrolled from the patients attending the department of Oral surgery, Tokyo Medical and Dental University, Dental hospital, who had a diagnosis of Oral lichen planus, and agreed to the consent for this study
Exclusion criteria
Exclusion criteria: the patients are a minor, and can not be given effective informed consent for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The degree of pain is assessed at baseline and at the three months after starting the treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| The clinical appearance is assessed at baseline and at the three months after starting the treatment | — |
Countries
Japan
Contacts
Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University Department of Oral and Maxillofacial Surgery