Ignite Creation Date:
2024-05-05 @ 4:43 PM
Last Modification Date:
2024-10-26 @ 9:23 AM
Study NCT ID:
NCT00294060
Status:
TERMINATED
Last Update Posted:
2011-05-06
First Post:
2006-02-16
Brief Title:
P3 Pacemaker Patient Profiling Study
Sponsor:
Medtronic Cardiac Rhythm and Heart Failure
Organization:
Medtronic Cardiac Rhythm and Heart Failure
Study Overview
Official Title:
Pacemaker Patient Profiling P3 Study
Status:
TERMINATED
Status Verified Date:
2011-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Preliminary analysis determined there was sufficient data to support objectives and allow early completion The last patient visit occurred on November 6 2007
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The P3 Study is a United States post market study to gather data on clinical status primary indications device therapy choices clinical management and outcomes for patients with implantable pacemakers
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