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ACTIVE NOT RECRUITING
NCT06606288

Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing (The CORE-CPP Study)

Sponsor: Medtronic Cardiac Rhythm and Heart Failure

View on ClinicalTrials.gov

Summary

The purpose of this study is to use real-world evidence to validate that conduction system pacing (CSP), delivered via a Medtronic 3830 catheter-delivered lead and a Medtronic dual-chamber transvenous pacemaker, is a safe and effective alternative to biventricular pacing (BVP) in patients indicated for cardiac resynchronization therapy (CRT) to deliver cardiac physiologic pacing (CPP), as documented in the clinical literature.

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

6000

Start Date

2017-01-01

Completion Date

2030-12-31

Last Updated

2025-03-26

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Conduction system pacing

Implant with a Medtronic dual-chamber transvenous pacemaker on or after the study data with lead type and placement data indicating conduction system pacing

DEVICE

Bi-ventricular pacing

Implant with a Medtronic bi-ventricular pacemaker (CRT-P) on or after the study date

Locations (1)

Medtronic

Mounds View, Minnesota, United States