跳至主要内容
临床试验/IRCT201407263566N4
IRCT201407263566N4已完成4 期

Comprative Efficiacy of Tacrolimus 0.1% vs flucinolone onitment in patients with cutaneous lichen planus

Vice chancellor for research, Tabriz University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
50

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

年龄范围
2 years 至 no limit(—)
性别
All

入选标准

  • patients with definite diagnose of lichen planus; patients older than 2 years.
  • Exclusion criteria: the presence of other skin diseases; patients using medication that can cause drug-induced lichen planus; history of drug reaction to steroid or Tacrolimus; pregnant women and lactating mothers; mental retarded or physically disabled patients.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research, Tabriz University of Medical Sciences

相似试验