Home › Ventricular Premature Complexes › NCT06060548
Role of Novel ILR in the Management of PVCs
RecruitingObservational study
Role of a Novel Implantable Loop Recorder in the Management of Premature Ventricular Contractions
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Patients \> 18 years of age * Have a Medtronic LINQ II ILR * Willing and able to give written informed consent Exclusion Criteria: * 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
About the study
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.
What is being tested
- Monitoring of patients presenting with PVCs (other)
Sponsor: Kansas City Heart Rhythm Research Foundation · Participants: 50 · Started: Apr 20, 2022
Contact the study team
- Donita Atkins · Phone: 816-651-1969
Official record on ClinicalTrials.gov — NCT06060548
Locations in the U.S.
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.