Monitoring of Syncopes and/or Sustained Palpitations of Suspected Arrhythmic Origin With External Loop-Recorder (SpiderFLASH)

NCT02253134 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 395

Last updated 2014-10-01

No results posted yet for this study

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.

Conditions

  • Syncope
  • Palpitations

Sponsors & Collaborators

  • LivaNova

    lead INDUSTRY

Principal Investigators

  • Emanuela T Locati · Azienda Ospedaliera Niguarda Ca' Granda - Milano

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • Belgium
  • Italy
  • Portugal
  • Spain
  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02253134 on ClinicalTrials.gov