跳至主要内容
临床试验/NCT04432103
NCT04432103终止3 期

Treatment of Severe and Critical COVID-19 Pneumonia With Convalescent Plasma

Centro Medico ABC2 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2020年8月8日最近更新:
适应症

试验速览

阶段
3 期
状态
终止
入组人数
6
试验地点
2
主要终点
INCIDENCE OF CRITICAL PNEUMONIA

研究概览

简要总结

Open label two arms, non randomized Convalescent Plasma treatment to severe and critical pneumonia COVID-19 hospitlaized patients compared to a historical cohort with matched controls.

详细描述

We will perform an open label two arms, non randomized trial giving Convalescent Plasma donated from recovered COVID-19 patients with positive serology to severe and clinical pneumonia COVID-19 patients admitted to the ABC Medical Center.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: >18 and <60 years
  • Body weight : >60 kg
  • Confirmed previous SARS CoV-2 infection
  • negative SARS CoV-2 test result
  • 21 day without symptoms from the negative SARS CoV2 negative test
  • Written informed consent to participate in this clinical trial, to donate plasma and to store the specimen for future testing.
  • Positive COVID-19 IgG antibodies
  • Male donors, or female donors who have not been pregnant, or female donors who have been pregnant tested negative for HLA antibodies
  • Individuals who meet all regular voluntary donor eligibility requirements by the Mexican legislation.
  • Patients/recipients:
  • Age: >18 years
  • Admitted to the ABC Medical Center facility for the treatment of COVID-19
  • Patients with severe or critical COVID-19
  • Informed consent provided by the patient or healthcare proxy

排除标准

  • Patients/recipients:
  • Contraindication to transfusion (severe volume overload, history of anaphylaxis to blood products)
  • Any other not controlled infection
  • Disseminated Intravascular Coagulopathy
  • Patient under dialysis
  • Patient with recent Hemorrhagic Stroke
  • Severe Ischemic Heart Disease

结局指标

主要结局

INCIDENCE OF CRITICAL PNEUMONIA

时间窗: 14 days after convalescent plasma administration

progression to critical stage

MORTALITY RATE AMONG CRITICAL PNEUMONIA PATIENTS

时间窗: 28 days after convalescent plasma administration

mortality

次要结局

  • INCIDENCE OF MECHANICAL VENTILATION(14 days after convalescent plasma treatment)
  • DAYS OF MECHANICAL VENTILATION(28 days after convalescent plasma treatment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验