TRIAGE-CRT Telemonitoring in Patients With CHF and Indication of CRT-D

PHASE4CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

January 31, 2008

Study Completion Date

January 31, 2008

Conditions
Congestive Heart FailureCardiac Resynchronization Therapy
Interventions
DEVICE

Kronos LV-T, Lumax HF-T

Implanted CRT-device sends out device diagnostics (e.g. heart rate, device and lead integrity, patient activity) via CardioMessenger on daily basis. In addition, daily weight and blood pressure readings are taken; remote data are analyzed by investigational sites via the internet on a weekly basis.

Trial Locations (12)

19718

Christiana Care Health Services, Wilmington

29303

Spartanburg Regional, Spartanburg

29506

Pee Dee Cardiology, Florence

30309

Piedmont Hospital, Atlanta

31201

Georgia Arrhythmia Consultants, Macon

44126

Cleveland Cardiovascular Research Foundation, Cleveland

48910

Thoracic & Cardiovascular Institute, Lansing

60135

Loyola University Medical Center, Chicago

63136

St. Louis Heart and Vascular, St Louis

85008

Maricopa Medical Center, Phoenix

85251

Scottsdale Cardiology, Scottsdale

02114

Massachusetts General Hospital, Boston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Biotronik, Inc.

INDUSTRY

NCT00395642 - TRIAGE-CRT Telemonitoring in Patients With CHF and Indication of CRT-D | Biotech Hunter | Biotech Hunter