Cardiac Implantable Electronic Device (CIED) Research Study

NCT05061862 · tracked via the Priya Life Science USA tracker

Sponsor

Medtronic Cardiac Rhythm and Heart Failure

Phase

Observational

Started

2022-03-06

Last updated

2025-12-10

Condition(s) studied

Arrhythmias, CardiacBradycardiaTachycardia

Investigational drug(s) / intervention(s)

cardiac implantable electronic devices (CIEDs)

cardiac implantable electronic devices (CIEDs): Subjects will be implanted with various cardiac implantable electronic devices and followed according to their standard of care. Medical imaging will be collected at various stages of the implant procedure and/or non-invasive diagnostic collection at follow-up visits, as applicable.

Study summary

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.

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

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

Primary outcome measure(s)

Product Development — 3 years
Characterize Cardiovascular Implantable Electronic Device (CIED) information, implant procedure details and/or patient characteristics to support development of future CIED products and procedures.

Trial sites (9)

Facility	City	Region
The Cardiac & Vascular Institute	Gainesville	Florida
Georgia Arrhythmia Consultants	Macon	Georgia
Oregon Health & Science University Hospital	Portland	Oregon
Lancaster General Hospital	Lancaster	Pennsylvania
Allegheny General Hospital	Pittsburgh	Pennsylvania
University of Virginia Medical Center	Charlottesville	Virginia
Inova Fairfax Hospital	Falls Church	Virginia
Sentara Norfolk General Hospital	Norfolk	Virginia
UZ Leuven - Campus Gasthuisberg	Leuven	Belgium

More Medtronic Cardiac Rhythm and Heart Failure trials in the USA

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Destination Therapy Post Approval Study Active, not recruiting

DelIVery for Pulmonary Arterial Hypertension (PAH) & Continued Support Study Active, not recruiting

Other trials for the same condition

Micra Transcatheter Pacing System Post-Approval Registry Active, not recruiting

Longitudinal Coverage With Evidence Development Study on Micra AV Leadless Pacemakers (Micra AV CED) Active, not recruiting

Enlighten Study: The EV-ICD Post Approval Registry Active, not recruiting

Aveir VR Coverage With Evidence Development Post-Approval Study Recruiting

Longitudinal Coverage With Evidence Development Study on Micra Leadless Pacemakers Active, not recruiting

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05061862 on ClinicalTrials.gov ↗ ← All trials in the USA