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Comparison of Medical Therapy, Pacing and Defibrillation in Heart Failure

Primary Purpose

Congestive Heart Failure

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cardiac Resynchronization Therapy with & without defibrillator
Sponsored by
Boston Scientific Corporation
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congestive Heart Failure focused on measuring Cardiac Resynchronization Therapy (CRT), Heart Failure, Defibrillator, Pacemaker

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: 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 Exclusion Criteria: 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 Amyloid disease Hospitalization for heart failure or IV inotropic or vasoactive therapy in excess of 4 hours in the 30 days prior to enrollment Have a tricuspid prosthesis Involved in any other investigational studies Life expectancy < 6 months due to any other medical conditions

Sites / Locations

  • Multiple locations in the US

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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

Full Information

First Posted
September 9, 2005
Last Updated
January 23, 2007
Sponsor
Boston Scientific Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT00180258
Brief Title
Comparison of Medical Therapy, Pacing and Defibrillation in Heart Failure
Official Title
Comparison of Medical Therapy, Pacing and Defibrillation in Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
January 2007
Overall Recruitment Status
Completed
Study Start Date
January 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2002 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Boston Scientific Corporation

4. Oversight

5. Study Description

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.
Detailed Description
Evaluation of new therapies for the treatment of heart failure should address mortality, morbidity, hospitalization, and cardiac symptoms and function when compared to standard pharmacologic therapy. The COMPANION trial is designed to address all of these objectives. This clinical investigation is an open-label, prospective, multi-center, randomized clinical trial. Every patient enrolled in the study is to be prescribed to optimal pharmacologic heart failure therapy, as tolerated, regardless of randomization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congestive Heart Failure
Keywords
Cardiac Resynchronization Therapy (CRT), Heart Failure, Defibrillator, Pacemaker

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Cardiac Resynchronization Therapy with & without defibrillator
Primary Outcome Measure Information:
Title
Combination of all-cause mortality and first hospitalization (time to first event), where all-cause mortality is defined as death from all causes.
Secondary Outcome Measure Information:
Title
Total survival for both the CONTAK CD and CONTAK TR CHFDs when used in conjunction with pharmacologic therapy.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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 Amyloid disease Hospitalization for heart failure or IV inotropic or vasoactive therapy in excess of 4 hours in the 30 days prior to enrollment Have a tricuspid prosthesis Involved in any other investigational studies Life expectancy < 6 months due to any other medical conditions
Facility Information:
Facility Name
Multiple locations in the US
City
St. Paul
State/Province
Minnesota
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15152059
Citation
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.
Results Reference
result
PubMed Identifier
35490339
Citation
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.
Results Reference
derived
PubMed Identifier
19204305
Citation
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.
Results Reference
derived

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Comparison of Medical Therapy, Pacing and Defibrillation in Heart Failure

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