InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry

CompletedOBSERVATIONAL
Enrollment

1,999

Participants

Timeline

Start Date

March 31, 2002

Primary Completion Date

April 30, 2011

Study Completion Date

April 30, 2011

Conditions
Heart FailureCardiomyopathy
Interventions
DEVICE

InSync Model 8040

Subjects with sucessful implants of InSync Model 8040.

DEVICE

InSync III Model 8042

Subjects with successful implants of InSync III Model 8042

Trial Locations (82)

Unknown

Birmingham

Peoria

Fort Smith

Little Rock

Long Beach

Napa

Oxnard

San Diego

Yuba City

Washington D.C.

Gainesville

Jacksonville

Jupiter

Melbourne

Miami

Orlando

Tampa

Atlanta

Rockford

Springfield

Indianapolis

Des Moines

Kansas City

Overland Park

Lexington

Louisville

Lake Charles

Shreveport

Baltimore

Salisbury

Silver Spring

Boston

Worchester

Detroit

Kalamazoo

Lansing

Marquette

Saginaw

Duluth

Minneapolis

Hattiesburg

Tupelo

Columbia

Kansas City

Saint Joseph

Springfield

St Louis

Billings

Lincoln

Newark

Manhasset

New York

Rochester

Chapel Hill

Charlotte

High Pointe

Raleigh

Winston-Salem

Cincinnati

Cleveland

Columbus

Mayfield Heights

Oklahoma City

Doylestown

Erie

Philadelphia

York

Providence

Greenville

Spartanburg

Nashville

Dallas

Fort Worth

Houston

Lubbock

Sherman

Salt Lake City

Richmond

Virginia Beach

Seattle

Morgantown

Milwaukee

All Listed Sponsors
lead

Medtronic Cardiac Rhythm and Heart Failure

INDUSTRY

NCT00273182 - InSync Model 8040 (InSync) and InSync III Model 8042 (InSync III) Registry | Biotech Hunter | Biotech Hunter