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临床试验/NCT04420988
NCT04420988No Longer Available不适用

Investigational COVID-19 Convalescent Plasma Infusion for Severely or Life-threateningly Ill COVID-19 Patients

Rutgers, The State University of New Jersey2 个研究点 分布在 1 个国家开始时间: 2020年6月9日最近更新:
适应症

试验速览

阶段
不适用
状态
No Longer Available
试验地点
2

研究概览

简要总结

This is an expanded access program providing COVID-19 convalescent plasma to patients hospitalized with severely or life-threateningly ill COVID-19.

详细描述

This expanded access program provides hospitalized patients who are severely or life-threateningly ill with COVID-19 access to investigational COVID-19 convalescent plasma (CCP). A clinical team comprised of Infectious Disease specialists, Pulmonary/Critical Care specialists and Hospitalists identify appropriate patients in accordance with FDA recommendations for patient eligibility and the daily availability of ABO-compatible CCP. CCP is obtained through New York Blood Center and American Red Cross in coordination with the University Hospital Blood Bank. Safety outcomes include monitoring for transfusion-related acute lung injury (TRALI), transfusion-associated circulatory overload (TACO) and any allergic reactions.Patients admitted to our institution prior to the availability of CCP will be separately reviewed.

研究设计

研究类型
Expanded Access

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

  • Laboratory confirmed COVID-
  • Severe or life-threatening COVID-
  • a) Severe disease is defined as one or more of the following: i) dyspnea, ii) respiratory frequency ≥ 30/min, iii) blood oxygen saturation ≤ 93%, iv) partial pressure of arterial oxygen to fraction of inspired oxygen ratio < 300, and/or v) lung infiltrates > 50% within 24 to 48 hours b) Life-threatening disease is defined as one or more of the following: i) respiratory failure, ii) septic shock, and/or iii) multiple organ dysfunction or failure

排除标准

  • Contraindication to transfusion (severe volume overload, history of anaphylaxis to blood products)
  • Severe multi-organ failure and hemodynamic instability requiring high doses of pressor agents
  • Other documented uncontrolled infection
  • Severe DIC needing factor replacement, FFP, cryoprecipitate
  • Acute renal failure requiring dialysis
  • Active intracranial bleeding
  • Clinically significant myocardial ischemia

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marc Klapholz, M.D.

Chair, Department of Medicine; Chief of Medicine Service, University Hospital

Rutgers, The State University of New Jersey

研究点 (2)

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