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临床试验/NL-OMON50782
NL-OMON50782
已完成
不适用

Researching the Effects of Sepsis on Quality Of life, Vitality, Epigenome and gene expression during RecoverY from sepsis (REQOVERY) - REQOVERY

niversitair Medisch Centrum Groningen0 个研究点目标入组 120 人待定

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
sepsis
发起方
niversitair Medisch Centrum Groningen
入组人数
120
状态
已完成
最后更新
去年

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
去年
研究类型
Observational invasive

研究者

入排标准

入选标准

  • Inclusion criteria sepsis group:
  • \- Adult patients, aged between 18 and 85 years
  • \- Able to provide informed consent themselves or informed consent can be
  • obtained via next of kin or legal guardian
  • \- Included in Acutelines, where blood sample were was drawn within 24 hours
  • upon of ED admission according to Acutelines protocol
  • \- Satisfy the Sepsis\-3 criteria for sepsis (Figure 2\), combined with clinical
  • suspicion of infection and/or fever (body temperature \> 38\.5°C)
  • \- Survive at 3 months post discharge
  • Inclusion criteria control group: adult patients, aged between 18 and 85 years

排除标准

  • \- Transfer from another hospital
  • \- Emergency room visit in connection with accidental exposure of bodily
  • material to patient (needle stick injury)
  • \- Visit an emergency room in connection with organ transplantation
  • \- Discharged home without hospital admittance after ED visit
  • \- Unable to give blood
  • \- Immunosuppressive therapies such as corticosteroids (\>10mg) or small molecule
  • immune suppressants within the last three months, or biologicals administered
  • within the last year
  • \- Radiotherapy or systemic chemotherapy within the last three months

结局指标

主要结局

未指定

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