Patient Preferences for Leadless Pacemakers

Completed

Conditions studied: Cardiac Rhythm Disorder, Bradycardia, Cardiac Pacemaker Artificial

In brief

Prospective, non-randomized, multi-center study designed to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers

Key facts

Study ID

NCT05327101

Run by

Abbott Medical Devices

People needed

117

Starts

2022-03-28

Expected to finish

2023-06-13

Last updated by the study team

2025-02-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Able to read and speak English to consent to participate in the survey
• Willing and able to use a tablet or computer to complete the survey
• Scheduled to undergo evaluation for a de novo cardiac pacemaker at the study site (patient may or may not have a known indication for a pacemaker at the time)

You may not qualify if…

• None

Where it is running

• Honor Health — Scottsdale, Arizona, United States
• Arrhythmia Research Group — Jonesboro, Arkansas, United States
• Arkansas Heart Hospital — Little Rock, Arkansas, United States
• Pacific Heart Institute — Santa Monica, California, United States
• Baptist Medical Center — Jacksonville, Florida, United States
• Rush University Medical Center — Chicago, Illinois, United States
• Prairie Education & Research Cooperative — Springfield, Illinois, United States
• Charlton Memorial Hospital — Fall River, Massachusetts, United States
• New York Presbyterian Hospital/Cornell University — New York, New York, United States
• Hightower Clinical — Oklahoma City, Oklahoma, United States
• University of Utah Hospital — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.