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
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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