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临床试验/DRKS00025079
DRKS00025079已完成不适用

Pilot study on the use of albumin function test by ESR method in ICU patients for the detection of sepsis/septic shock and its follow-up.

MedInnovation GmbH0 个研究点目标入组 26 人开始时间: 2021年4月28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
26

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 one(—)
性别
All

入选标准

  • Sepsis Group
  • - At least 18 years
  • - Patients diagnosed with sepsis as defined by Sepsis-3 (life-threatening organ dysfunction caused by a dysregulated immune response to infection.
  • Clinical Criteria: SOFA score =2, screening tool: qSOFA at least 2 of 3 (AF=22/min; RR syst. =100mmHg; impaired mental status: GCS<15).
  • Septic shock
  • - At least 18 yrs.
  • - Septic shock = sepsis + cardiovascular collapse unresponsive to hydration and vasopressors necessary to maintain MAP > 65mmHg, lactate = 2 mmol/L
  • Control group
  • - At least 18 yrs.
  • - Patient -of the intensive care unit of the Internal Medicine of the University Medical Center Rostock without sepsis / septic shock.
  • - If sepsis / septic shock occurs within 7 days, the patient will be kept as control group 2, but an additional control patient without sepsis / septic shock will be included in the study
  • Translated with www.DeepL.com/Translator (free version)

排除标准

  • Extracorporeal treatment with citrate anticoagulation ongoing at the time of blood collection;
  • Albumin substitution;
  • More than 500ml of FFP or red cell concentrate 12 hours prior to blood collection;
  • Patients with liver cirrhosis;

研究者

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