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临床试验/IRCT20210901052358N3
IRCT20210901052358N3尚未招募未知

Comparisson of the effectiveness of Tocilizumab and Tofacitinib on the outcomes of patients with severe COVID-19

Shahid Beheshti 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
未知
状态
尚未招募
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 no limit(—)
性别
All

入选标准

  • Laboratory confirmation of COVID-19 virus by PCR
  • Severe cases according to the World Health Organization guideline (peripheral blood oxygen saturation less than 90%, respiratory rate more than 30 per minute or symptoms of severe respiratory distress such as use of auxillary respiratory muscles or inability to complete sentences)
  • Body mass index less than 40 kg per square meter
  • No immunosuppressive diseases (primary, secondary and organ transplant defects, chemotherapy or radiotherapy)
  • Patient willingness to participate in the study
  • Non-pregnant and non-lactating women
  • Serum CRP level greater than 75 mg / L
  • Do not receive immunomodulatory drugs for 6 months before
  • No history of severe hypersensitivity to tosilizumab and tofacitinib and similar compounds
  • No history of active gastric ulcer, active diverticulitis and other gastrointestinal diseases with risk of intestinal perforation
  • No active hepatitis or tuberculosis or a bacterial or fungal or viral infection other than COVID-19
  • No history of chronic kidney disease (GFR less than 30 ml / min)

排除标准

  • Severe drug allergy and anaphylactic shock
  • Death in the first 24 hours of hospitalization
  • Increase in liver enzymes to more than 10 times the normal upper limit
  • Decrease in neutrophil count to less than 500 cells per microliter
  • Decrease in platelet count to less than 50,000 cells per microliter
  • GFR less than 30 ml per minute

研究者

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