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临床试验/IRCT20200314046764N1
IRCT20200314046764N1已完成3 期

The evaluation of pirfenidone effects on prevention and treatment of pulmonary fibrosis and acute respiratory distress syndrome caused by COVID-19

Kermanshah University of Medical Sciences0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
40

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

  • Confirmed cases of New coronavirus infection or COVID-19 who are 18 years and older;
  • Not more than 14 days from the onset of symptoms
  • Bilateral lung involvement in imaging findings
  • Moderate to severe acute respiratory distress syndrome
  • Decreased PaO2 to FiO2 ratio

排除标准

  • AST and ALT> 3-5x ULN at visit and bilirubin> 1.5 x ULN at visit
  • creatinine clearance rate calculated by Cockcroft-Gault formula at visit 1 <30 mL / min
  • Confirmed previous Idiopathic pulmonary fibrosis,previous treatment with Nidanib or Pirfenidone
  • Significant pulmonary hypertension (PAH)
  • Cardiovascular diseases, including any of the following diseases: ? Severe hypertension within 6 months of Visit 1, uncontrollable after treatment (=160 / 100 mmHg); ? myocardial infarction within 6 months of visit 1; ? unstable angina within 6 months of visit 1
  • history of severe central nervous system (CNS) events
  • known trials Drug allergies
  • Patients unable to follow the trial procedures
  • Breastfeeding

研究者

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