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临床试验/NCT07490314
NCT07490314已完成不适用

Blood Product Supply During COVID-19

Methodist Health System1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
Time frame

研究概览

简要总结

Data about the links between Coronavirus disease 2019(COVID-19) and the safety of blood products during the pandemic is inadequate. During the COVID-19 pandemic, high volumes of patients receiving blood products due to post-terminal surgical complications depleted stores for the entire hospital, resulting in surgeons unable to acquire emergent blood products. Data from this study can be used to develop a policy on how to handle blood shortage issues during this and future pandemics. Also, this data can be used to determine future policies on use of blood products from COVID-19-positive donors.

详细描述

  • To identify the circumstances associated with observed delays in receiving blood products to use in emergent cases.
  • Determine the cost/benefit of moribund patients receiving massive transfusion during the COVID-19 pandemic.
  • Quantify COVID-19 diagnosis and complications in patients arriving with no indication of disease at index admission as relative to in hospital or blood product exposure.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

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

  • >_18 years of age Surgical patients treated at Methodist Dallas Medical Center(MDMC)

排除标准

  • <18 years of age Prisoners Pregnant women

结局指标

主要结局

Time frame

时间窗: 1 year

Dates of inadequate or delayed blood products for emergent cases during the timeframe of the COVID-19 pandemic (March 2020 to March 2021) to be compared relative to number of days or cases where no shortages were noted

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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