NCT00180258

Brief Summary

The purpose of this study is to determine whether combined mortality and hospitalization in heart failure patients receiving optimal pharmacologic therapy can be reduced by combining optimal pharmacologic therapy and 1) biventricular pacing therapy alone or 2) biventricular pacing with defibrillation.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,200

participants targeted

Target at P75+ for phase_2

Timeline
Completed

Started Jan 2000

Typical duration for phase_2

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2000

Completed
2.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2002

Completed
2.8 years until next milestone

First Submitted

Initial submission to the registry

September 9, 2005

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 16, 2005

Completed
Last Updated

January 25, 2007

Status Verified

January 1, 2007

First QC Date

September 9, 2005

Last Update Submit

January 23, 2007

Conditions

Keywords

Cardiac Resynchronization Therapy (CRT)Heart FailureDefibrillatorPacemaker

Outcome Measures

Primary Outcomes (1)

  • Combination of all-cause mortality and first hospitalization (time to first event), where all-cause mortality is defined as death from all causes.

Secondary Outcomes (1)

  • Total survival for both the CONTAK CD and CONTAK TR CHFDs when used in conjunction with pharmacologic therapy.

Interventions

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Moderate or severe heart failure, defined as symptomatic heart failure for at least six months with NYHA Class III or IV symptoms at the time of enrollment, AND at least one of the following events in the previous 12 months:
  • Hospitalization for heart failure management
  • Outpatient visit in which intravenous (IV) inotropes or vasoactive infusion were administered continuously for at least 4 hours
  • Emergency room visit of at least twelve hours duration in which IV heart failure medications were administered (including diuretics)
  • QRS \> or = 120 ms and PR interval \> 150 ms from any two leads of a 12-lead ECG
  • Left ventricular ejection fraction \< or = 35%
  • Left ventricular end diastolic dimension \> or = 60 mm (required only if LVEF measured by echo) or \> 3.0 cm/m2 \[The cm/m2 is calculated by LVEDD (in cm) divided by BSA (body surface area)\].
  • Age \> or = 18 years
  • Optimal pharmacologic therapy for heart failure

You may not qualify if:

  • Unable or unwilling to undergo device implant and follow-up testing
  • Meet the general indications for an implantable cardioverter defibrillator
  • Meet the general indications for antibradycardia pacing
  • Expected to receive a heart transplant in the next six months
  • Chronic, medically refractory atrial tachyarrhythmias
  • Unexplained syncope
  • Myocardial infarction within 60 days of randomization
  • History of non-compliance with oral heart failure therapy
  • Progressive or unstable angina
  • Uncontrolled blood pressure: Systolic BP \> 160 mm Hg or \< 85 mm Hg or diastolic BP \> 90 mm Hg
  • Patients with a hypersensitivity to a 0.7 mg nominal dose of dexamethasone acetate
  • Surgically uncorrected primary valvular heart disease
  • Coronary artery disease (CAD) in which surgical or percutaneous correction is recent (within 60 days of randomization)
  • Women who are pregnant or not using medically acceptable birth control
  • Hypertrophic obstructive cardiomyopathy
  • +5 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Multiple locations in the US

Saint Paul, Minnesota, United States

Location

Related Publications (3)

  • Bristow MR, Saxon LA, Boehmer J, Krueger S, Kass DA, De Marco T, Carson P, DiCarlo L, DeMets D, White BG, DeVries DW, Feldman AM; Comparison of Medical Therapy, Pacing, and Defibrillation in Heart Failure (COMPANION) Investigators. Cardiac-resynchronization therapy with or without an implantable defibrillator in advanced chronic heart failure. N Engl J Med. 2004 May 20;350(21):2140-50. doi: 10.1056/NEJMoa032423.

  • Cleland JGF, Bristow MR, Freemantle N, Olshansky B, Gras D, Saxon L, Tavazzi L, Boehmer J, Ghio S, Feldman AM, Daubert JC, de Mets D. The effect of cardiac resynchronization without a defibrillator on morbidity and mortality: an individual patient data meta-analysis of COMPANION and CARE-HF. Eur J Heart Fail. 2022 Jun;24(6):1080-1090. doi: 10.1002/ejhf.2524. Epub 2022 May 22.

  • Anand IS, Carson P, Galle E, Song R, Boehmer J, Ghali JK, Jaski B, Lindenfeld J, O'Connor C, Steinberg JS, Leigh J, Yong P, Kosorok MR, Feldman AM, DeMets D, Bristow MR. Cardiac resynchronization therapy reduces the risk of hospitalizations in patients with advanced heart failure: results from the Comparison of Medical Therapy, Pacing and Defibrillation in Heart Failure (COMPANION) trial. Circulation. 2009 Feb 24;119(7):969-77. doi: 10.1161/CIRCULATIONAHA.108.793273. Epub 2009 Feb 9.

MeSH Terms

Conditions

Heart Failure

Interventions

Cardiac Resynchronization TherapyDefibrillators

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Cardiac Pacing, ArtificialElectric Stimulation TherapyTherapeuticsElectrodesElectrical Equipment and SuppliesEquipment and Supplies

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY

Study Record Dates

First Submitted

September 9, 2005

First Posted

September 16, 2005

Study Start

January 1, 2000

Study Completion

December 1, 2002

Last Updated

January 25, 2007

Record last verified: 2007-01

Locations