RECRUITING

Role of Novel ILR in the Management of PVCs

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2022-04-20
Study Completion:2025-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06060548

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients \> 18 years of age
  2. * Have a Medtronic LINQ II ILR
  3. * Willing and able to give written informed consent
  1. * History of myocardial infarction
  2. * Significant flow-limiting coronary artery disease (≥50% stenosis) on invasive coronary angiography or Computed tomography angiography (CTA).
  3. * History of cardiac arrest
  4. * With existing implantable defibrillators
  5. * Currently pregnant

Contacts and Locations

Study Contact

Donita Atkins
CONTACT
816-651-1969
datkins@kchrf.com

Principal Investigator

Dhanunjaya Lakkireddy, MD
PRINCIPAL_INVESTIGATOR
Kansas City Heart Rhythm Institute

Study Locations (Sites)

Kansas City Heart Rhythm Institute - Roe Clinic
Overland Park, Kansas, 66211
United States
Overland Park Regional Medical Center
Overland Park, Kansas, 66215
United States
Centerpoint Medical Center Clinic
Independence, Missouri, 64057
United States
Centerpoint Medical Center
Independence, Missouri, 64057
United States
Research Medical Center Clinic
Kansas City, Missouri, 64032
United States
Research Medical Center
Kansas City, Missouri, 64032
United States

Collaborators and Investigators

Sponsor: Kansas City Heart Rhythm Research Foundation

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

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-04-20
Study Completion Date2025-03

Study Record Updates

Study Start Date2022-04-20
Study Completion Date2025-03

Terms related to this study

Additional Relevant MeSH Terms

  • PVC - Premature Ventricular Contraction
  • Myocarditis