Viewing Study NCT06606288



Ignite Creation Date: 2024-10-25 @ 8:01 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06606288
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: None
First Post: 2024-09-18

Brief Title: Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing The CORE-CPP Study
Sponsor: None
Organization: None

Study Overview

Official Title: Characterizing Outcomes and Real-World Experience of Cardiac Physiologic Pacing The CORE-CPP Study
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CORE-CPP
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None