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NCT01498146 Clinical Trial

Finding Atrial Fibrillation in Patients With Unexplained Stroke Using Longterm Cardiac Monitoring

Stroke Clinical Trial

— SURPRISE  

Official title:
Stroke Prior to Diagnosis of Atrial Fibrillation Using Longterm Observation With Implantable Cardiac Monitoring Apparatus Reveal(SURPRISE) -the SURPRISE Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01498146
Other study ID # H-4-2010-014
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2010
Est. completion date October 2013

Study information
Verified date January 2021
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The SURPRISE study investigates atrial fibrillation(AFIB) in patients with a previous unexplained stroke. It uses long term monitoring of the heart of up to three years, searching for paroxysmal atrial fibrillation(PAF) otherwise undetected in this population.

Description:

The SURPRISE study investigates the patients with cryptogenic stroke or transient ischemic attack (TIA), monitoring them with a cardiac loop recorder for up to three years. it aims at estimating the amount of paroxysmal atrial fibrillation within our population of cryptogenic stroke patients. Standard workup for a stroke patient does offer cardiac evaluation, but monitoring is limited to the time admitted, often just a few days.

Recruitment information / eligibility
Status Completed
Enrollment 85
Est. completion date October 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender All
Age group 18 Months and older
Eligibility Inclusion Criteria: - Computerized Tomography (CT) or Magnetic resonance imaging (MRI) verified cryptogenic stroke or TIA; - > 18 years of age, - the ability to provide a written consent Exclusion Criteria: - prior or known AFIB - AF found during work up including 24 hour telemetric monitoring.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Denmark Bispebjerg Hospital, University Hospital of Copenhagen, dept of Neurology Copenhagen

Sponsors (1)
Lead Sponsor Collaborator
Bispebjerg Hospital

Country where clinical trial is conducted

Denmark, 

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