Ignite Creation Date:
2024-05-05 @ 4:35 PM
Last Modification Date:
2024-10-26 @ 9:21 AM
Study NCT ID:
NCT00271232
Status:
COMPLETED
Last Update Posted:
2007-12-21
First Post:
2005-12-28
Brief Title:
InSync III Marquis Model 7279 Cardioverter Defibrillator Cardiac Resynchronization System
Sponsor:
Medtronic Cardiac Rhythm and Heart Failure
Organization:
Medtronic Cardiac Rhythm and Heart Failure
Study Overview
Official Title:
InSync III Marquis Model 7279 Cardioverter Defibrillator Cardiac Resynchronization System
Status:
COMPLETED
Status Verified Date:
2007-12
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:
None
Brief Summary:
People who have a dangerously fast heart beat or whose heart is at risk of stopping beating may be in need of an electronic device called an implantable cardioverter defibrillator ICD An ICD is implanted surgically just under the skin in the upper chest area and it sends a strong electrical impulse or shock to the heart to return it to a normal rhythm If the heart is beating too slowly or at an abnormal rhythm an ICD can also pace the heart to return the heart to its normal rhythm
The InSync III Marquis device can change the timing of when the left and right ventricles of the heart are paced to beat This is called V to V timing V to V timing may further improve the pumping function of the heart The purpose of this study is to determine whether or not this V to V timing feature of the InSync III Marquis system is safe and effective
The InSync III Marquis device can change the timing of when the left and right ventricles of the heart are paced to beat This is called V to V timing V to V timing may further improve the pumping function of the heart The purpose of this study is to determine whether or not this V to V timing feature of the InSync III Marquis system is safe and effective
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