跳至主要内容
临床试验/CTRI/2020/04/024915
CTRI/2020/04/024915尚未招募2 期

A Phase II, Open Label, Randomized Controlled Trial to Assess the Safety and Efficacy of Convalescent Plasma to Limit COVID-19 Associated Complications

Max Super Speciality Hospital A Unit of Devki Devi Foundation0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

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

入选标准

  • 1. Patients admitted with RT-PCR confirmed COVID-19 illness.
  • 2. Age > 18 years
  • 3. Written informed consent
  • 4. Has any of the two
  • a. PaO2/ FiO2 <300
  • b. Respiratory Rate > 24/min and SaO2 < 93% on room air

排除标准

  • 1. Pregnant women
  • 2. Breastfeeding women
  • 3. Known hypersensitivity to blood products
  • 4. Receipt of Pooled Immunoglobulin in last 30 days
  • 6. Participating in any other clinical trial
  • 7. Clinical status precluding infusion of blood products

研究者

发起方
Max Super Speciality Hospital A Unit of Devki Devi Foundation

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