Cardiac Implantable Electronic Device (CIED) Research Study
Status: Recruiting
Location: See all (9) locations...
Intervention Type: Device
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Subject is at least 18 years of age.
• Subject is willing and able to provide written informed consent.
• Subject is willing and able to complete the study procedures and visits for the duration of data collection requirements
Locations
United States
Florida
The Cardiac & Vascular Institute
TERMINATED
Gainesville
Georgia
Georgia Arrhythmia Consultants
TERMINATED
Macon
Oregon
Oregon Health & Science University Hospital
NOT_YET_RECRUITING
Portland
Pennsylvania
Lancaster General Hospital
TERMINATED
Lancaster
Allegheny General Hospital
RECRUITING
Pittsburgh
Virginia
University of Virginia Medical Center
NOT_YET_RECRUITING
Charlottesville
Inova Fairfax Hospital
NOT_YET_RECRUITING
Falls Church
Sentara Norfolk General Hospital
TERMINATED
Norfolk
Other Locations
Belgium
UZ Leuven - Campus Gasthuisberg
NOT_YET_RECRUITING
Leuven
Contact Information
Primary
Amy A Lautenbach, MAOL
amy.a.lautenbach@medtronic.com
(763)360-9163
Time Frame
Start Date: 2022-03-06
Estimated Completion Date: 2026-05-01
Participants
Target number of participants: 1000
Treatments
CIED Indicated Subjects
Subjects indicated to receive a cardiac implantable electronic devices (CIEDs)
Related Therapeutic Areas
Sponsors
Leads: Medtronic Cardiac Rhythm and Heart Failure