CTRI/2023/03/051002尚未招募Unknown
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 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •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.
排除标准
- •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
研究者
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