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临床试验/IRCT20200428047232N1
IRCT20200428047232N1已完成3 期

Effectiveness and safety of thalidomide in moderate COVID-19 pneumonia: A randomized 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
已完成
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
  • Percentage of oxygen saturation at the time of admission: 89-85% (provided it is modified with Nazal auxiliary oxygen to more or equal to 90%) or oxygen saturation percentage of 90-93% and the number of breaths per minute more or equal to 30
  • Clinical manifestations associated with COVID-19 pneumonia with positive PCR test or HR-CT scan

排除标准

  • Previous Chronic lung disease
  • Multi-organ failure at admission

研究者

相似试验

Effect of Thalidomide in Covid 19 pneumonia | 临床试验