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NCT02155907

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

Completed Last updated 7 May 2018
What this trial tests

trial in Stroke in 1,507 participants. Completed in 31 December 2017.

Timeline
1 June 2013
Primary endpoint
31 December 2017
31 December 2017

Quick facts

Lead sponsorUniversity of Aarhus
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,507
Start date1 June 2013
Primary completion31 December 2017
Estimated completion31 December 2017
Sites1 location across Denmark

Conditions studied

Sponsor

University of Aarhus

Who can join

60 and older, any sex, with Stroke or Ischaemic Stroke. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. External continuous ECG versus loop recording for atrial fibrillation detection in patients who had a stroke.
    Sejr MH, May O, Damgaard D, Sandal BF, et al · · 2019 · cited 10× · PMID 30898849 · DOI 10.1136/heartjnl-2018-314186

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Other recruiting trials for Stroke

Currently open trials in the same condition.

Other University of Aarhus trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02155907.

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