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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

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 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
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

Find a Location

Who is running the clinical trial?

Kansas City Heart Rhythm Research FoundationLead Sponsor
27 Previous Clinical Trials
11,298 Total Patients Enrolled
14 Trials studying Atrial Fibrillation
3,634 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
~1667 spots leftby Sep 2025
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