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ICM for Atrial Fibrillation
N/A
Recruiting
Led By Dhanunjaya Lakkireddy
Research Sponsored by Kansas City Heart Rhythm Research Foundation
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 12 months
Awards & highlights
Study Summary
Observational, multi-center, retrospective study to evaluate the use of ICM (implantable cardiac monitor) versus traditional, non-ICM (non-implantable cardiac monitor) methods such as ECGs (electrocardiogram), Holter, and mobile cardiac outpatient telemetry (MCOT) units.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
No.of patients with arrhythmia recurrence
No.of patients with redo ablation
Trial Design
2Treatment groups
Experimental Treatment
Group I: Non-ICMExperimental Treatment1 Intervention
Patients with traditional monitoring methods
Group II: ICMExperimental Treatment1 Intervention
Patients who underwent ICM insertion
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Who is running the clinical trial?
Kansas City Heart Rhythm Research FoundationLead Sponsor
26 Previous Clinical Trials
9,472 Total Patients Enrolled
13 Trials studying Atrial Fibrillation
1,808 Patients Enrolled for Atrial Fibrillation
Dhanunjaya LakkireddyPrincipal InvestigatorKansas City Heart Rhythm Institute
11 Previous Clinical Trials
6,586 Total Patients Enrolled
6 Trials studying Atrial Fibrillation
726 Patients Enrolled for Atrial Fibrillation
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