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临床试验/NCT03107637
NCT03107637已完成不适用

Therapeutic Implications of Early Transesophageal Echocardiography in Embolic Stroke of Undetermined Source (ESUS)

Fondation Ophtalmologique Adolphe de Rothschild1 个研究点 分布在 1 个国家目标入组 186 人开始时间: 2016年10月3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
186
试验地点
1
主要终点
therapeutic modification after transesophageal echocardiography

研究概览

简要总结

The ESUS concept was introduced recently to describe a non-lacunar stroke of undetermined etiology. The following etiological workup is required in this setting: head CT or MRI, 12-lead ECG, transthoracic echocardiography, continuous cardiac monitoring for at least 24 hours after stroke, vascular imaging (ultrasound, magnetic resonance angiography, CT angiography, catheter angiography). Transesophageal echocardiography (TEE) is considered not to be required.

However, aortic arch atheroma as diagnosed by TEE in the setting of recent ischemic stroke is a major aortic source of embolism, as supported by numerous well conducted studies. The European Association of Echocardiography considers that TEE is the gold standard for the diagnosis and the characterization of aortic atheroma. It is also the method of choice for the diagnosis of infectious endocarditis.

The aim of this work was to evaluate the rate of patients with a therapeutic modification induced by TEE (mainly anticoagulation and surgery), in consecutive patients admitted with ESUS at our institution stroke unit.

研究设计

研究类型
Observational
观察模型
Other
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

  • Presenting with a new onset of ischemic stroke
  • Meeting the ESUS criteria (Embolic Stroke of Undetermined Source)
  • Comprehensive transthoracic echo prior to the TEE

排除标准

  • ESUS criteria not met
  • Contraindications to TEE
  • TEE failure
  • Pregnant or breastfeeding woman
  • Person under legal protection
  • No medical insurance coverage

结局指标

主要结局

therapeutic modification after transesophageal echocardiography

时间窗: 24 hours after TEE

proportion of patients with a therapeutic modification (mainly anticoagulation and surgery)

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

研究点 (1)

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