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临床试验/NL-OMON49795
NL-OMON49795招募中3 期

Convalescent Plasma Therapy from Recovered Patients to Treat COVID-19 Early in SARS-CoV-2 Disease - CoV-Early

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 690 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
690

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 至 99(—)

入选标准

  • PCR-confirmed COVID-19
  • Symptomatic (e.g but not limited to fatigue, fever, cough, dyspnoe, loss of
  • taste or smell, diarrhea, falls or confusion)
  • 70 years or older OR 50-69 years and 1 or more of the risk factors described
  • 1. A/ Medical history
  • Obesity with BMI 35 or higher
  • Born as a male person
  • History of cardiac or pulmonary disease (e.g. but not limited to atrial
  • fibrillation, coronary artery disease, heart failure, COPD, asthma)
  • History of neurological disease (e.g. a history of stroke or any other
  • chronic debilitating neurological disease)
  • Diabetes for which medical therapy is needed
  • Chronic kidney disease with GFR <60 ml/min
  • Reumatic disease (e.g. reumatoid arthritis, Systemic lupus erythematosus,
  • psoriatric artritis)
  • Immunodeficiency (e.g. organ or allogeneic transplantation, systemic
  • immunosuppressive drugs)
  • Cancer not in complete remission for >1 year (excluding baso -or
  • spinocellular skin cancers)
  • Untreated HIV and CD4 T-cells <200/microliter
  • Chronic liver disease, liver cirrhosis
  • 1. B/ Lab results (if available)
  • CRP > 30
  • SARS-CoV-2 RT-PCR Ct value <25

排除标准

  • Life expectancy <28 days in the opinion of the treating physician
  • Patient or legal representative is unable to provide written informed consent
  • Symptomatic for 8 days or more
  • Being admitted to the hospital at the informed consent procedure
  • Known previous history of transfusion-related acute lung injury
  • Known IgA deficiency

研究者

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