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Clinical Trials/NCT02351076
NCT02351076
Completed
Not Applicable

Correlation of Right-left Shunt Detection in Cardioembolism Etiology in Stroke Patient. Pilot Study.

University Hospital Ostrava1 site in 1 country44 target enrollmentAugust 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Foramen Ovale Patent
Sponsor
University Hospital Ostrava
Enrollment
44
Locations
1
Primary Endpoint
detection of right-to-left shunt
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The aim of the study is to compare correlation for right to left shunts (mainly patent foramen ovale) detection for three methods-transesophageal echo as a gold standard, transcranial doppler with contrast agent (microbubbles) and new method- Flow detection system ( Cardiox TM) in young stoke patients ( age under 55 years).

Detailed Description

The aim of the study is to compare correlation for right to left shunts (mainly patent foramen ovale) detection for three methods-transesophageal echo as a gold standard, transcranial doppler with contrast agent (microbubbles) and new method- Flow detection system ( Cardiox TM) in young stoke patients ( age under 55 years). Flow detection systém is a new method for right to left shunt detection comfortable for patients, not dependent on experienced examinator and only one method with exact valsalve maneuver measurement. Right to left shunt could be important etiology of cardioembolization in young stroke patient population, therefore screening for this condition is recommended in all young patient after ischemic stroke especially with unclear etiology. Flow detection systes seams to be ideal screening method for this patients.

Registry
clinicaltrials.gov
Start Date
August 2014
End Date
August 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital Ostrava
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ischemic stroke / TIA, signed informed consent -

Exclusion Criteria

  • imposibillity to undergo transesophageal echo, transcranial doppler with contrast or Cardiox flow detection system

Outcomes

Primary Outcomes

detection of right-to-left shunt

Time Frame: 1 week

Correletation of right-to-left shunt detection by 3 methods: transesophageal echocardiography, transcranial Doppler with contrast agent (microbubbles) and Flow detection system (Cardiox TM)

Study Sites (1)

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