Cardiac Implantable Electronic Device (CIED) Research Study
Running, not enrolling
Conditions studied: Arrhythmias, Cardiac, Bradycardia, Tachycardia
In brief
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.
Key facts
- Study ID
- NCT05061862
- Run by
- Medtronic Cardiac Rhythm and Heart Failure
- People needed
- 1000
- Starts
- 2022-03-06
- Expected to finish
- 2026-05-01
- Last updated by the study team
- 2025-12-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Subject is unwilling or unable to comply with study procedures as defined in the protocol.
- Subject with a medical condition that precludes the patient from participation in the opinion of the investigator.
- Subject is enrolled in another study that could confound the results of this study, without documented pre-approval from a Medtronic study manager.
Where it is running
- The Cardiac & Vascular Institute — Gainesville, Florida, United States
- Georgia Arrhythmia Consultants — Macon, Georgia, United States
- Oregon Health & Science University Hospital — Portland, Oregon, United States
- Lancaster General Hospital — Lancaster, Pennsylvania, United States
- Allegheny General Hospital — Pittsburgh, Pennsylvania, United States
- University of Virginia Medical Center — Charlottesville, Virginia, United States
- Inova Fairfax Hospital — Falls Church, Virginia, United States
- Sentara Norfolk General Hospital — Norfolk, Virginia, United States
- UZ Leuven - Campus Gasthuisberg — Leuven, Belgium
Full record on ClinicalTrials.gov
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