SCD-HeFT10 Yr: SCD-HeFT 10 Year Follow-up

Sponsor

Seattle Institute for Cardiac Research (Other)

Overall Status

Unknown status

CT.gov ID

NCT01058837

Collaborator

National Institutes of Health (NIH) (NIH), Abbott Medical Devices (Industry)

1,855

Enrollment

Location

Duration (Months)

80.8

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

No clinical trial that has examined the role of implantable cardioverter defibrillator (ICD) therapy in the prevention of Sudden Cardiac Death (SCD) has provided outcome data for longer than a few years. The NHLBI sponsored and placebo-controlled Sudden Cardiac Death in heart Failure Trial (SCD-HeFT) conducted from 1997 to 2003 had the largest number of patients and the longest average follow-up at 45.5 months. This study changed the national reimbursement policy for ICD therapy and remains the reference point for all other ICD evaluations in patients with congestive heart failure from ischemic or non-ischemic systolic dysfunction. Despite the outcome, the role of ICD therapy in the management of patients with heart failure has been questioned because of four principal concerns: numbers needed to treat to save a life, lead integrity over time, the negative consequences of shock therapy, and the cost of therapy. The purpose of this trial is to track down the remaining patients for a one-time follow-up regarding key outcome data.

Condition or Disease	Intervention/Treatment	Phase
Left Ventricular Systolic Dysfunction Congestive Heart Failure Ischemic and Non-ischemic Cardiomyopathy Sudden Cardiac Death Primary Prevention

Detailed Description

Long-term outcome data for implantable cardioverter defibrillator (ICD) therapy is sorely needed. We will acquire these data by re-approaching the patient population from the original Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT).[Bardy 2005] This research is supported by the National Heart Lung and Blood Institute of the National Institutes of Health.

SCD-HeFT was originally conducted from 1997 to 2003. It demonstrated unequivocally that ICD's save lives in patients with heart failure compared to placebo or amiodarone. More than 26 peer-reviewed publications, including three NEJM papers, have resulted from this work.[Bardy 2005, Poole 2008, Mark 2008] Despite the quality of SCD-HeFT and the evidence of the life-saving ability of ICD therapy, the role of ICD therapy in the management of patients with heart failure continues to be questioned. This study will provide long-term follow-up of the SCD-HeFT patients, which will now exceed 10 years on average.

Study Design

Study Type:

Observational

Anticipated Enrollment :

1855 participants

Observational Model:

Case-Control

Time Perspective:

Cross-Sectional

Official Title:

Sudden Cardiac Death in Heart Failure Trial 10 Year Follow-up (SCD-HeFT 10 Year)

Study Start Date :

Sep 1, 2009

Anticipated Primary Completion Date :

Aug 1, 2011

Anticipated Study Completion Date :

Aug 1, 2011

Outcome Measures

Primary Outcome Measures

To compare 10-year mortality data on the remaining 1855 SCD-HeFT patients since the close of follow-up from October 31, 2003 in the 3 arms of the trial (ICD, placebo and amiodarone)based upon an intent-to-treat and an on-treatment analysis. [Two years]

Secondary Outcome Measures

To obtain outcome data in the major subgroups of SCD-HeFT: ischemic v. non-ischemic and NYHA Class II vs. Class III heart failure, and in woman and minorities. [Two years]
To obtain 10-year ICD use rates (appropriate and inappropriate therapy), complication rates, lead failure rates and replacement rates. [Two Years]
To validate or refute the observation that amiodarone increases mortality in NYHA Class III patients. [Two years]
To obtain 10-year hospitalization and major procedure data. [Two years]
To obtain 10-year quality of life data. [Two years]