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临床试验/NCT05231720
NCT05231720Unknown不适用

Mannheim Register of Sepsis and Septic Shock

Universitätsmedizin Mannheim2 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2019年12月3日最近更新:
适应症

试验速览

阶段
不适用
入组人数
500
试验地点
2
主要终点
all-cause mortality

研究概览

简要总结

The study aims to investigate clinically and prognostically relevant parameters in patients with sepsis and septic shock within a monocentric observational clinical register.

详细描述

All consecutive septic patients at the internists intensive care Unit (ICU) at the University of Mannheim are included in the register and follow up during ICU stay and after that. Data of patients' admission status, septic focus, baseline parameters, and comorbidities are collected. Extensive information about echocardiography, electrocardiography, and imaging procedures are included in the register. Laboratory values, microbiological investigations, organ dysfunction and organ replacement therapies, medication, adverse events, and complications were recorded for several days during the ICU stay (days 1, 2,3, 5,7, and 10). Standard scores for critically ill patients were calculated for the day before admission at the ICU if available, and several time points during the ICU stay. The register includes information about the mortality during ICU stay, 30-day mortality, 6-month mortality, and septic patients' 1-year mortality.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者

入选标准

  • Sepsis and septic shock according to current guidelines

排除标准

  • other forms of shock not associated with an infection

结局指标

主要结局

all-cause mortality

时间窗: 30 days

次要结局

  • all-cause mortality(12 months)

研究者

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

Michael Behnes

Prof. Dr.

Universitätsmedizin Mannheim

研究点 (2)

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Mannheim Register of Sepsis and Septic Shock | 临床试验