ACTIVE_NOT_RECRUITING

Cardiac Implantable Electronic Device (CIED) Research Study

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Conditions

Arrhythmias, CardiacBradycardiaTachycardia

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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

The study is designed to collect data on Cardiovascular Implantable Electronic Device (CIED) information, implant procedure details, and/or patient characteristics to support development of future CIED products and procedures.

Official Title

Cardiac Implantable Electronic Device (CIED) Research Study

Quick Facts

Study Start:2022-03-06
Study Completion:2026-05-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05061862

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. 1. Subject is at least 18 years of age.
  2. 2. Subject is willing and able to provide written informed consent.
  3. 3. Subject is willing and able to complete the study procedures and visits for the duration of data collection requirements
  1. 1. Subject is unwilling or unable to comply with study procedures as defined in the protocol.
  2. 2. Subject with a medical condition that precludes the patient from participation in the opinion of the investigator.
  3. 3. Subject is enrolled in another study that could confound the results of this study, without documented pre-approval from a Medtronic study manager.

Contacts and Locations

Study Locations (Sites)

The Cardiac & Vascular Institute
Gainesville, Florida, 32605
United States
Georgia Arrhythmia Consultants
Macon, Georgia, 31201
United States
Oregon Health & Science University Hospital
Portland, Oregon, 97239
United States
Lancaster General Hospital
Lancaster, Pennsylvania, 17604
United States
Allegheny General Hospital
Pittsburgh, Pennsylvania, 15212
United States
University of Virginia Medical Center
Charlottesville, Virginia, 22903
United States
Inova Fairfax Hospital
Falls Church, Virginia, 22042
United States
Sentara Norfolk General Hospital
Norfolk, Virginia, 23507
United States

Collaborators and Investigators

Sponsor: Medtronic Cardiac Rhythm and Heart Failure

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 Date2022-03-06
Study Completion Date2026-05-01

Study Record Updates

Study Start Date2022-03-06
Study Completion Date2026-05-01

Terms related to this study

Additional Relevant MeSH Terms

  • Arrhythmias, Cardiac
  • Bradycardia
  • Tachycardia