跳至主要内容
临床试验/IRCT20170207032444N3
IRCT20170207032444N3招募中3 期

The efficacy and safety of Thalidomide in severe Covid19 pneumonia: Arandomized controlled clinical trial

Esfahan University of Medical Sciences0 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
招募中
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
18 years 至 75 years(—)
性别
All

入选标准

  • 18-75 year old men and 50-75 year old women admitted in hospital
  • Spo2 less than 85% in admission
  • Clinical symptoms and signs compatible with COVID19 infection and positive PCR test or lung HRCT abnormalities compatible with COVID19 pneumonia
  • No need to intubation in first 24 hour of admission
  • No multiorgan failure at presentation
  • No shock state at presentation
  • Obtained informed consent

排除标准

  • Hepatic failure (Child Pugh score = C, AST> 5 times of the upper limit normal)
  • Severe renal dysfunction (GFR less than 30cc per min)

研究者

相似试验

Thalidomide in COVID19 | 临床试验