Ignite Creation Date:
2024-05-06 @ 6:53 PM
Last Modification Date:
2024-10-26 @ 2:56 PM
Study NCT ID:
NCT05822791
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-03-13
First Post:
2023-03-31
Brief Title:
Differences in ECG- vs proLonged cardIac MonItor-DeTected Atrial Fibrillation in STROKE Patients DELIMIT AF-STROKE
Sponsor:
Lawson Health Research Institute
Organization:
Lawson Health Research Institute
Study Overview
Official Title:
Differences in ECG- vs proLonged cardIac MonItor-DeTected Atrial Fibrillation in STROKE Patients
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The present study is an investigator-initiated single-center retrospective study based on data from the London Ontario Stroke Registry LOSR aiming to compare the characteristics and outcomes of ECG-detected and Device-Detected atrial fibrillation in patients with ischemic stroke and transient ischemic attack
Detailed Description:
Patients with ischemic stroke and transient ischemic attack TIA without known atrial fibrillation AF are investigated with Prolonged Cardiac Monitoring PCM to detect AF It is unclear if AF detected on 12-lead ECG after stroke occurrence bears the same risk of stroke as Device-detected AF The investigators hypothesize that Device-detected AF has a lower risk of ischemic stroke recurrence The investigators will conduct a retrospective analysis of prospectively collected data from consecutive patients enrolled in the London Ontario Stroke Registry Ontario Canada The primary outcome will be a recurrent ischemic stroke at the end of the available follow-up window The investigators will include ischemic stroke and TIA patients with ECG-detected AF and those with Device-detected AF on at least 7 days of Holter monitoring
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None