To test the effectiveness of two commonly used medicines in Oral Lichen Planus and to study their molecular interactions.
Not Applicable
- Conditions
- Health Condition 1: K00-K14- Diseases of oral cavity and salivary glands
- Registration Number
- CTRI/2023/08/056156
- Lead Sponsor
- MGM Dental College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Clinico- histopathologically diagnosed cases of Oral Lichen
Planus.
1. Patients with symptoms of pain and burning sensation
secondary to Oral Lichen Planus.
2. Patients willing to participate in the study
Exclusion Criteria
Topical or systemic medication for treatment of Oral Lichen Planus up to 4 weeks prior to the study
Histopathological examination with atypical or lichenoid
dysplastic features.
1. Patients with asymptomatic oral lesions.
2. Patients with other mucosal diseases.
3. Patients with history of any allergy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To check and compare the reduction in clinical signs and symptoms of Oral Lichen Planus on application of treatment agents during the course of followup <br/ ><br>Timepoint: 0,2,4,6,8 weeks
- Secondary Outcome Measures
Name Time Method ilTimepoint: NI