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Clinical Trial Summary

The main hypothesis of this work is that an approach combining clinical parameters and biomarker assays could improve the understanding and prediction of the occurrence of silent atrial fibrillation (AF) in the acute phase after stroke. In this prospective work, the investigators will rely on the Dijon Stroke Registry, which collects extensive clinical data for each patient hospitalized for a stroke. As part of this registry, patients are seen 6 months after stroke to assess their clinical status. This clinical follow-up will allow us to judge the evolution of the AF diagnosed during the acute episode at a distance.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03570060
Study type Observational
Source Centre Hospitalier Universitaire Dijon
Contact Charles GUENANCIA
Phone 0380293535
Email charles.guenancia@chu-dijon.fr
Status Recruiting
Phase
Start date April 1, 2018
Completion date April 2025

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