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临床试验/NCT03663192
NCT03663192已完成不适用

Strain Echocardiography During Septic Shock : an Observational Pilot Study

Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2016年2月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Global peak systolic longitudinal strain assessed by echocardiography. Global peak systolic longitudinal strain

研究概览

简要总结

The mortality of septic shock remains high nowadays despite a trend toward improvement.Septic cardiomyopathy has been reported in most experimental models of sepsis shock. Its relationship with mortality is unclear. A decrease in mortality have been reported in patients with decreased left ventricular ejection fraction (LVEF), but a recent meta-analysis did not support such results. In fact, it appears that high LVEF are linked to profound vasoplegia which is associated to bad outcome.

In the other hand, alterations of Strain echocardiography, a new method allowing a more sensitive evaluation of heart function, have been associated with a worse outcome in sepsis patients. Only few studies have examined echocardiographic strain during sepsis shock in human, and its natural history was only described in pigs. Moreover, the right ventricular strain was reported only by Orde et al whereas the evolution of strain during fluid infusion have never been studied. The aim of the present study is to describe the natural history of echocardiographic strain during sepsis shock and to determine its prognosis value.

研究设计

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

入排标准

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

入选标准

  • Septic shock (suspected or proven infection and norepinephrine ≥ 0,25µg/kg/min)
  • Inclusion within the first 24h of septic shock

排除标准

  • Patient < 18 year of age
  • Pregnant women
  • History of myocardial infarction, valvular disease, atrial fibrillation

结局指标

主要结局

Global peak systolic longitudinal strain assessed by echocardiography. Global peak systolic longitudinal strain

时间窗: up to 90 days

次要结局

  • ICU mortality(up to 90 days)

研究者

发起方
Centre Hospitalier Universitaire de Nīmes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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