跳至主要内容
临床试验/IRCT20141209020250N4
IRCT20141209020250N4招募中3 期

Evaluation of the efficacy and side effects of topical diphencyprone with or without topical anthralin in patients with moderate to severe alopecia areata referring to Razi Hospital Diphencyprone Clinic, 2018- 2019.

Tehran University of Medical Sciences0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
40

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
18 years 至 65 years(—)
性别
All

入选标准

  • moderate to severe alopecia areata

排除标准

  • pregnancy or lactation
  • receiving systemic immunosuppressive therapy during recent 3 months
  • severe systemic disease (eg. hepatic or renal failure )
  • immunosuppression
  • past history of severe reaction or intolerance to diphencyprone or anthralin
  • inability to follow regular visits or cooperation with investigators
  • participation in another clinical trial in recent 4 weeks
  • recent active sever progressive hair loss requiring systemic immunosuppressive therapy

研究者

相似试验