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临床试验/IRCT20200130046311N1
IRCT20200130046311N1已完成未知

Comparative evaluation of the response rate based on tricoscopic criteria in patients with severe alopecia areata treated with diphencyprone with or without intralesional platelet rich plasma

Tehran University of Medical Sciences0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
20

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 no limit(—)
性别
All

入选标准

  • A patient with alopecia areata whose definitive diagnosis was made on clinical or histological basis and their involvement was severe (> 50% scalp area and less than 100%).
  • Positive response to test with 2% Diphen Ciprone solution

排除标准

  • Patients with alopecia totalis or universalis
  • Receive any systemic treatment during the last 6 months
  • Children under 18 years
  • Pregnant and lactating women
  • Immunosuppressed patient
  • patient with platelet dysfunction
  • patient with a history of injecting steroids on the site over the past month
  • Fever, systemic infection and local infection at the injection site

研究者

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