跳至主要内容
临床试验/IRCT20210823052264N2
IRCT20210823052264N2尚未招募3 期

Efficacy of Acyclovir in Pityriasis rosea, a double blind randomized controlled trial in a tertiary care hospital in Pakistan.

PNS SHIFA0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
60

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
12 years 至 70 years(—)
性别
All

入选标准

  • Patients presenting with pityriasis rosea within first week of eruption of papulosquamous rash.
  • Either gender between Age 12-70 years.

排除标准

  • Positive venereal disease research laboratory (VDRL) test.
  • Females with pregnancy or lactation.
  • Patients who have taken any other specific treatment for PR in last 01 week.
  • Patients with any cause of immunosuppression like chronic renal failure, diabetes mellitus, HIV positive and malignancy etc.

研究者

发起方
PNS SHIFA

相似试验

Efficacy of Acyclovir in Pityriasis rosea | 临床试验