Role of Novel ILR in the Management of PVCs

Description

This prospective, observational study is a single center clinical registry of patients referred for management of symptomatic or asymptomatic Premature Ventricular Contractions (PVCs). Subjects will be followed through 12 months. The study will enroll approximately 50 patients.

Conditions

PVC - Premature Ventricular Contraction, Myocarditis

Study Overview

Study Details

Study overview

This prospective, observational study is a single center clinical registry of patients referred for management of symptomatic or asymptomatic Premature Ventricular Contractions (PVCs). Subjects will be followed through 12 months. The study will enroll approximately 50 patients.

Role of a Novel Implantable Loop Recorder in the Management of Premature Ventricular Contractions

Role of Novel ILR in the Management of PVCs

Condition
PVC - Premature Ventricular Contraction
Intervention / Treatment

-

Contacts and Locations

Overland Park

Kansas City Heart Rhythm Institute - Roe Clinic, Overland Park, Kansas, United States, 66211

Overland Park

Overland Park Regional Medical Center, Overland Park, Kansas, United States, 66215

Independence

Centerpoint Medical Center Clinic, Independence, Missouri, United States, 64057

Independence

Centerpoint Medical Center, Independence, Missouri, United States, 64057

Kansas City

Research Medical Center Clinic, Kansas City, Missouri, United States, 64032

Kansas City

Research Medical Center, Kansas City, Missouri, United States, 64032

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patients \> 18 years of age
  • * Have a Medtronic LINQ II ILR
  • * Willing and able to give written informed consent
  • * History of myocardial infarction
  • * Significant flow-limiting coronary artery disease (≥50% stenosis) on invasive coronary angiography or Computed tomography angiography (CTA).
  • * History of cardiac arrest
  • * With existing implantable defibrillators
  • * Currently pregnant

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Kansas City Heart Rhythm Research Foundation,

Dhanunjaya Lakkireddy, MD, PRINCIPAL_INVESTIGATOR, Kansas City Heart Rhythm Institute

Study Record Dates

2025-03