Skip to content

Transesophageal Echocardiography in Embolic Stroke of Undetermined Source

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03107637
Acronym
ETO
Enrollment
186
Registered
2017-04-11
Start date
2016-10-03
Completion date
2019-01-31
Last updated
2021-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Embolic Stroke of Undetermined Source, Ischemic Stroke

Keywords

Embolic Stroke of Undetermined Source, transesophageal echocardiography, cardiac source of embolism, ischemic stroke

Brief summary

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.

Interventions

None listed

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
therapeutic modification after transesophageal echocardiography24 hours after TEEproportion of patients with a therapeutic modification (mainly anticoagulation and surgery)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026