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Clinical Trial Summary

The purpose of this study is to evaluate the diagnostic yield (at 1 month post enrollment) of an external loop recorder (SpiderFlash-T) in patients with syncope or palpitations of suspected arrhythmic origin, within 30 days before enrollment.


Clinical Trial Description

Diagnostic yield (primary outcome) definition = Number of patients with conclusive diagnosis (as per investigators' decision) over the total number of patients ;


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02253134
Study type Observational
Source LivaNova
Contact
Status Completed
Phase N/A
Start date August 2010
Completion date June 2013

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