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Atrial Fibrillation Detected by ELR and Holter Recording, a Comparison in Patients With Ischemic Stroke or TIA

NCT02155907 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1507

Last updated 2018-05-07

No results posted yet for this study

Summary

Purpose

1. To validate 2 -day loop recording ( R.Test Evolution 4 ) to 2 -day Holter recording (gold standard) for the detection of atrial fibrillation of ≥ 30 seconds duration in a consecutive population of patients with stroke or transient ischemic attack (TIA).
2. To determine whether short run of atrial fibrillation (\< 30s ) or the presence of many supraventricular extrasystoles detected on Holter recording, is associated with risk of re-stroke in a consecutive population of patients with stroke or TIA .
3. To test whether a 7-day Loop Recording (R -test) detects more patients with atrial fibrillation than 2 days of Holter recording in a consecutive population of patients with stroke or TIA.

Conditions

Sponsors & Collaborators

  • Hospitalsenheden Vest

    collaborator OTHER

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Michala H Sejr, MD · University of Aarhus

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-01
Primary Completion
2017-12-31
Completion
2017-12-31

Countries

  • Denmark

Study Locations

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Entities

Diseases

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 NCT02155907 on ClinicalTrials.gov