CTRI/2023/03/051002
Not yet recruiting
未知
Randomised clinical trial to study the clinical efficacy of oral apremilast with topical triamcinolone acetonide versus topical triamcinolone acetonide alone (standard care) in oral lichen planus.
All India Institute of Medical Sciences, Jodhpur0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: L438- Other lichen planus
- Sponsor
- All India Institute of Medical Sciences, Jodhpur
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a) Patients with clinical diagnoses of oral lichen planus or biopsy proven oral lichen planus.
- •b) Age more than 16 years
- •c) Treatment wash off period of 2 weeks for topical drugs and 4 weeks for immunosuppressive drugs.
Exclusion Criteria
- •a) Pregnant and lactating women
- •b) Hypersensitivity to oral apremilast
- •c) Known case of renal and hepatic impairment
- •d) Known case of psychiatric disease
- •e) Patients with extensive cutaneous involvement secondary to lichen planus.
- •f) Patients with dental restoration in situ
Outcomes
Primary Outcomes
Not specified
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