1,024
Participants
Start Date
June 30, 2004
Primary Completion Date
March 31, 2008
Study Completion Date
June 30, 2008
Cardiac Resynchronization Therapy Device
Patients with an ICD indication, a CRT indication and symptomatic heart failure who are implanted with a Cardiac Resynchronization Therapy Device.
Huntsville
Phoenix
Scottsdale
Little Rock
Loma Linda
San Diego
Denver
Guilford
Bradenton
Fort Lauderdale
Key Largo
Melbourne
Miami
Orlando
Palm Beach Gardens
Pensacola
Safety Harbor
Tallahassee
Tampa
Winter Park
Atlanta
Augusta
Honolulu
Evanston
Maywood
Merrionette Park
Rockford
Springfield
Winfield
Topeka
Wichita
Edgewood
Florence
Louisville
Covington
Monroe
Portland
Salisbury
Takoma Park
Grand Rapids
Marquette
Petoskey
Traverse City
Minneapolis
Saint Cloud
St Louis
Missoula
Las Vegas
Manchester
Cherryhill
Ridgewood
Sewell
New York
The Bronx
West Islip
Williamsville
Charlotte
Durham
Greensboro
Raleigh
Bismarck
Fargo
Cincinnati
Columbus
Dayton
Elyria
Lakewood
Mayfield Heights
Westlake
Medford
Camp Hill
Erie
Philadelphia
Pittsburgh
Wormleysburg
York
Pawtucket
Providence
Columbia
Spartanburg
Sioux Falls
Knoxville
Nashville
Fairfax
Fort Worth
Lubbock
Burlington
Lynchburg
Norfolk
Richmond
Kirkland
Green Bay
Madison
Collaborators (1)
Medtronic
INDUSTRY
Medtronic Cardiac Rhythm and Heart Failure
INDUSTRY