Status:
COMPLETED
PARTNERS HF: Program to Access and Review Trending Information and Evaluate Correlation to Symptoms in Patients With Heart Failure
Lead Sponsor:
Medtronic Cardiac Rhythm and Heart Failure
Collaborating Sponsors:
Medtronic
Conditions:
Heart Failure, Congestive
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to determine the value of diagnostic data obtained from Medtronic implantable cardioverter defibrillators (ICDs) with cardiac resynchronization therapy (CRT) to evaluate c...
Eligibility Criteria
Inclusion
- Patients who meet the ICD indications
- Patients with Class III or IV heart failure.
- Patients receiving or who received a Medtronic CRT ICD within the previous 3 months.
- Patient must sign and date informed consent, and be 18 years of age or greater.
- Patient must be available for follow up visits, and be willing and able to comply with study protocol.
Exclusion
- Patient with acute myocardial infarction (MI), coronary artery bypass graft surgery (CABG) or percutaneous coronary angioplasty (PTCA)/stent within the last month.
- Patient with a mechanical right heart valve.
- Patient with chronic (permanent) atrial arrhythmias.
- Patient with life expectancy of less than 12 months.
- Patient with status post heart transplant
- Patient undergoing kidney dialysis
- Patients enrolled in a concurrent study that may confound the results of the study.
Key Trial Info
Start Date :
June 1 2004
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2008
Estimated Enrollment :
1024 Patients enrolled
Trial Details
Trial ID
NCT00279955
Start Date
June 1 2004
End Date
June 1 2008
Last Update
June 15 2012
Active Locations (93)
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1
Huntsville, Alabama, United States
2
Phoenix, Arizona, United States
3
Scottsdale, Arizona, United States
4
Little Rock, Arkansas, United States