Oral Lichen Planus Clinical Trial
Official title:
Comparison of Triamcinolone Acetonide Mucoadhesive Film and Licorice Mucoadhesive Film Effect on the Duration and Symptoms of Lesions That Caused by Symptomatic Oral Lichen Planus
Verified date | May 2015 |
Source | Isfahan University of Medical Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | Iran: Ministry of Health |
Study type | Interventional |
Introduction :Oral lichen planus (OLP) is one of the most common disorders of the oral
cavity which is basically a chronic and inflammated mucocutaneous .There is no cure for OLP
currently. The main focus of treatment is to reduce the duration and severity of the
symptoms. This study was designed to determine and compare the parameters of improvement in
patient symptoms and lesions caused by oral lichen planus by using triamcinolone acetonide
mucoadhesive film and licorice mucoadhesive film.
Methods and materials :The study was randomized by double-blind clinical trial . Patients
with symptomatic OLP who referred to the Oral Medicine School of Dentistryin Medical
Sciences in Isfahan University participated voluntarily. The patients were divided into two
groups that were including 30 samples in each group. The first group was treated with
triamcinolone mucoadhesive film and the second group were treated with licorice mucoadhesive
film. Data were analyzed by using the Mann-Whitney test and t-test in SPSS software.
Status | Completed |
Enrollment | 60 |
Est. completion date | April 2015 |
Est. primary completion date | March 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - All patients over 18 years old - All non pregnant women Exclusion Criteria: |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Isfahan University of Medical Sciences |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | VAS | Pain severity was measured by visual analogue scale : 0 for no pain and 10 for most painful experience | 12 months | Yes |
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