Role of Novel ILR in the Management of PVCs

Recruiting now

Conditions studied: PVC - Premature Ventricular Contraction, Myocarditis

In brief

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.

Key facts

Study ID

NCT06060548

Run by

Kansas City Heart Rhythm Research Foundation

People needed

50

Starts

2022-04-20

Expected to finish

2025-12-01

Last updated by the study team

2025-08-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients > 18 years of age
• Have a Medtronic LINQ II ILR
• Willing and able to give written informed consent

You may not qualify if…

• 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

Where it is running

• Kansas City Heart Rhythm Institute - Roe Clinic — Overland Park, Kansas, United States (enrolling)
• Overland Park Regional Medical Center — Overland Park, Kansas, United States (enrolling)
• Centerpoint Medical Center Clinic — Independence, Missouri, United States (enrolling)
• Centerpoint Medical Center — Independence, Missouri, United States (enrolling)
• Research Medical Center Clinic — Kansas City, Missouri, United States (enrolling)
• Research Medical Center — Kansas City, Missouri, United States (enrolling)

Full record on ClinicalTrials.gov

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