Clinico-pathological study of Lichen Planus
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Cutaneous and oral lichen planus
- Registration Number
- CTRI/2013/04/003567
- Lead Sponsor
- Teena Ramesh M
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Both sexes aged 18 years and above.
Patients willing for the required investigation with a written informed consent.
Untreated, newly detected cases of lichen planus.
Exclusion Criteria
Patients not willing to give consent.
Age less than 18 years.
Immunocompromised patients and pregnant women.
Patients who have taken treatment for lichen planus within the past three months.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method clinical and histopathologicalprofile of patients with lichen planusTimepoint: 1 year
- Secondary Outcome Measures
Name Time Method Immunohistochemical analysis for CD4+ and CD8+ T-cell subsetsTimepoint: 1 year