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临床试验/SLCTR/2022/012
SLCTR/2022/012尚未招募4 期

Comparison of the effectiveness and safety of hydroxychloroquine and methotrexate in the treatment of moderate to severe oral lichen planus

Department of Pharmacology, Faculty of Medicine, University of Peradeniya0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
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

  • 1. Age 18-60 years, both male and female.
  • 2. Patients with histologically confirmed moderate to severe OLP with or without skin involvement (a pain score of 6 or greater on a VAS of 0 to 10)
  • 3. Histological confirmation of diagnosis from an incisional biopsy from oral mucosa
  • 4. Sinhala / English speaking patients

排除标准

  • 1. Patients with psychiatric disorders
  • 2. Pregnant or lactating women (to exclude pregnancy in premenopausal women, treatment will be commenced after the next menstrual period or if still unsure, after a negative urine hCG test.)
  • 3. Patients with contraindications for HCQ or MTX
  • 4. Patients with poorly controlled diabetes
  • 5. Patients with known retinal diseases
  • 6. Patients with other dermatological conditions in addition to LP
  • 7. Patients who have received treatment for LP previously
  • 8. Patients with contraindications to long-term steroids

研究者

发起方
Department of Pharmacology, Faculty of Medicine, University of Peradeniya

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