Screening for Atrial Fibrillation, After Ischemic Stroke
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|ClinicalTrials.gov Identifier: NCT01160406|
Recruitment Status : Completed
First Posted : July 12, 2010
Last Update Posted : June 27, 2011
The aim of the study is to assess the incidence of patients suffering from ischemic stroke or transient ischemic attacks who have underlying asymptomatic paroxysmal atrial fibrillation.
Patients who have suffered an ischemic stroke or transient ischemic attack, without a history of atrial fibrillation, are planned to be included. Starting within 14 days of the ischemic stroke, participating patients are asked to perform 10 second ECG recordings using a handheld ECG device twice daily (mornings and evenings) during 30 days. These recordings are transmitted via telephone to a secure encrypted Internet site. Within these 30 days the participants also perform an ambulatory 24 hour Holter recording. Handheld ECG recordings are evaluated continuously. In case of atrial fibrillation the patient is informed and offered treatment with anti coagulant medication (Warfarin). The investigation is a comparison between 24 hour continuous ECG recordings and short intermittent ECG recordings twice daily over a longer time period to determine which method is the best to detect atrial fibrillation in this patient group.
Hypothesis: Short Intermittent ECG recordings over a longer time period is more efficient, compared with continuous 24 hour ECG recordings, in detecting silent paroxysmal AF in patients with an ischemic stroke and without a history of atrial fibrillation.
|Condition or disease|
|Atrial Fibrillation Stroke|
|Study Type :||Observational|
|Estimated Enrollment :||250 participants|
|Official Title:||Improving Screening for Silent Atrial Fibrillation, After Ischemic Stroke|
|Study Start Date :||June 2007|
|Primary Completion Date :||November 2010|
|Study Completion Date :||November 2010|
ischemic stroke, no atrial fibrillation
Patients who have suffered ischemic stroke or transient ischemic attack without known atrial fibrillation
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01160406
|Halmstad, Halland, Sweden, 30180|
|Stockholm, Sweden, 11883|
|Danderyds hospital AB|
|Stockholm, Sweden, 18288|
|Study Director:||Mårten Rosenqvist, M.D.Ph.D.||Karolinska Institutet|