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Cardiac Monitor
Reveal LINQ™ Insertable Cardiac Monitor for Stroke
N/A
Waitlist Available
Research Sponsored by Medtronic Cardiac Rhythm and Heart Failure
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 years
Awards & highlights
Study Summary
This study is evaluating whether continuous cardiac rhythm monitoring can detect atrial fibrillation in people with a recent stroke.
Eligible Conditions
- Stroke
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The Rate of AF Through 12 Months in Subjects With a Recent Ischemic Stroke of Presumed Known Origin.
Secondary outcome measures
The Rate of AF Through the Duration of Study Follow-up (36 Months) Between Study Arms.
Trial Design
2Treatment groups
Active Control
Group I: Control ArmActive Control1 Intervention
Subjects randomized to the control arm will be followed per site specific standard of care.
Group II: Reveal LINQ™ Insertable Cardiac MonitorActive Control1 Intervention
Subjects randomized to the Reveal LINQ™ Insertable Cardiac Monitor arm will be continuously monitored via the inserted Reveal LINQ™ device.
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Who is running the clinical trial?
Medtronic Cardiac Rhythm and Heart FailureLead Sponsor
198 Previous Clinical Trials
128,434 Total Patients Enrolled
2 Trials studying Stroke
3,547 Patients Enrolled for Stroke
Richard Bernstein, PhD/MDStudy ChairNorthwestern
Lee Schwamm, MDStudy ChairMass General
1 Previous Clinical Trials
88 Total Patients Enrolled
1 Trials studying Stroke
88 Patients Enrolled for Stroke
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