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临床试验/NCT03796715
NCT03796715已完成不适用

Comparison of Red Cell Distribution Width Versus Presepsin (Soluble CD14) for Prognosis Assessment in Sepsis Patients Admitted to the Intensive Care Unit

Ain Shams University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年8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
200
试验地点
1
主要终点
Mortality during intensive care unit stay

研究概览

简要总结

Presepsin (soluble CD14 subtype) is a novel marker with growing body of evidence supporting its accuracy and value for the diagnosis of sepsis. Patients with sepsis showed higher Prsepsin levels compared to those with SIRS. In addition the increase in Prsepsin levels correlates well with sepsis severity. Red cell distribution width variations are increased in a variety of medical conditions such as congestive heart failure, acute myocardial infarction, pulmonary embolism, pneumonia, critical illness, and cardiac arrest , and is a predictor of mortality in the general population. we aim to compare between Presepsin (soluble CD14) and RDW as prognostic markers in critically-ill patients with sepsis.

研究设计

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

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female aged 18 65 years.
  • Appropriate clinical data to enable classification into sepsis or SIRS according to Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).
  • Written informed consent by the patient or guardian

排除标准

  • No informed consent
  • Renal failure
  • Liver failure
  • Hematologic diseases
  • Neutropenia
  • Malignancy
  • Chemotherapy during the previous 90 days.
  • Patients using antibiotics at presentation

结局指标

主要结局

Mortality during intensive care unit stay

时间窗: 28 days

次要结局

  • Need for readmission to ICU(assessed up to 3 months)
  • Ventilatory support duration(assessed up to 3 months)
  • Number of participants who need inotropic or vasopressor support(assessed up to 3 months)
  • Length of ICU stay(assessed up to 3 months)
  • Number of participants who need renal replacement therapy(assessed up to 3 months)
  • Transfusion requirements (blood and blood products)(assessed up to 3 months)

研究者

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

Ahmed Elsayed

Principal Investigator

Ain Shams University

研究点 (1)

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