Cardiac Implantable Electronic Device (CIED) Research Study

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.

Conditions

Arrhythmias, Cardiac, Bradycardia, Tachycardia

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Study Overview

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Study Details

Study overview

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.

Cardiac Implantable Electronic Device (CIED) Research Study

Cardiac Implantable Electronic Device (CIED) Research Study

Condition
Arrhythmias, Cardiac
Intervention / Treatment

-

Contacts and Locations

Gainesville

The Cardiac & Vascular Institute, Gainesville, Florida, United States, 32605

Macon

Georgia Arrhythmia Consultants, Macon, Georgia, United States, 31201

Portland

Oregon Health & Science University Hospital, Portland, Oregon, United States, 97239

Lancaster

Lancaster General Hospital, Lancaster, Pennsylvania, United States, 17604

Pittsburgh

Allegheny General Hospital, Pittsburgh, Pennsylvania, United States, 15212

Charlottesville

University of Virginia Medical Center, Charlottesville, Virginia, United States, 22903

Falls Church

Inova Fairfax Hospital, Falls Church, Virginia, United States, 22042

Norfolk

Sentara Norfolk General Hospital, Norfolk, Virginia, United States, 23507

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.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • 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.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Medtronic Cardiac Rhythm and Heart Failure,

Study Record Dates

2028-05-01