Comparing Oral Tofacitinib and Topical Triamcinolone Acetonide for Oral Lichen Planus: A Randomized Trial
Phase 2
- Conditions
- Health Condition 1: L438- Other lichen planus
- Registration Number
- CTRI/2024/07/070729
- Lead Sponsor
- ostgraduate Institute of Medical Education and Research Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Clinician-confirmed diagnosis of symptomatic oral lichen planus having exclusive oral involvement or predominant oral involvement with few cutaneous lesions
2. Patients aged between 18-60 years of age
3. Patients providing informed consent and are willing to follow up monthly for at least 6 months
Exclusion Criteria
1. Pregnant and lactating women
2. Women with childbearing potential who are unwilling to follow reliable methods of contraception
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method