跳至主要内容
临床试验/TCTR20201022004
TCTR20201022004招募中不适用

Effectiveness and Safety of Recombinant Human Erythropoietin on Patient Survival Rate during Severe Sepsis

one0 个研究点目标入组 300 人开始时间: 2020年10月22日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
one
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 99 Years(—)
性别
All

入选标准

  • 1.Participants who admitted to intensive care unit due to sepsis/ septic shock.
  • 2.Participants who age of 18 years or older with received erythropoietin according to their underlying disease.

排除标准

  • 1. Participants with missing clinical and laboratory data.
  • 2. Participants who have been referred to another hospital.
  • 3. Participants who have been treated with alternate to standard sepsis bundle scheme for sepsis and/or septic shock treatment as described in sepsis management guidelines.

研究者

发起方
one

相似试验