Viewing Study NCT00268294



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Last Modification Date: 2024-10-26 @ 9:21 AM
Study NCT ID: NCT00268294
Status: COMPLETED
Last Update Posted: 2008-12-18
First Post: 2005-12-21

Brief Title: Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial Fibrillation ReSync AF
Sponsor: Medtronic Cardiac Rhythm and Heart Failure
Organization: Medtronic Cardiac Rhythm and Heart Failure

Study Overview

Official Title: Restoring Sinus Rhythm With Cardiac Resynchronization in Patients With Atrial Fibrillation
Status: COMPLETED
Status Verified Date: 2008-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Heart failure is a progressive disease that decreases the pumping action of the heart This may cause a backup of fluid in the heart and may result in heart beat changes When there are changes in the heart beat sometimes an implantable heart device is used to control the rate and rhythm of the heart beat In certain heart failure cases when the two lower chambers of the heart no longer beat in a coordinated manner cardiac resynchronization therapy may be prescribed

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

Atrial tachyarrhythmia AT is the name for rapid beats in the upper chambers of the heart People with AT may experience symptoms such as heart palpitations a racing or pounding feeling in the chest shortness of breath dizziness fatigue or weakness

The purpose of this study is to characterize the impact of cardiac resynchronization therapy versus cardiac resynchronization therapy with atrial therapies on the incidence duration and termination of atrial tachyarrhythmias
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