PACMAN - PAcing for CardioMyopathies, a EuropeAN Study
Primary Purpose
Heart Failure
Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Contak heart failure devices
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure
Eligibility Criteria
Inclusion Criteria: - NYHA Class III and IV with EF < 35%; Optimal individual drug therapy in 2 weeks prior to enrollment including ACE inhibitors; beta blockers and diuretics unless not tolerated Exclusion Criteria: Reduced life expectancy of < 6 months or candidate for heart transplant within 6 months; chronic/recurrent atrial fibrillation/flutter
Sites / Locations
- Guidant Corporation, , , Belgium
- Medizinische Klinik I, University RWTH Aachen
Outcomes
Primary Outcome Measures
Improvement in functional capacity as measured by a six-minute walk test at 6 months
Secondary Outcome Measures
Improvement in Quality of Life at 6 months; Improvement in NHYA classification at 6 months; incidence of adverse events at 6 months
Full Information
NCT ID
NCT00180596
First Posted
September 15, 2005
Last Updated
January 5, 2016
Sponsor
Boston Scientific Corporation
1. Study Identification
Unique Protocol Identification Number
NCT00180596
Brief Title
PACMAN - PAcing for CardioMyopathies, a EuropeAN Study
Official Title
Pacing for Cardiomyopathies, a European Study- A Therapy Acceptance Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2005
Overall Recruitment Status
Completed
Study Start Date
January 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2005 (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Boston Scientific Corporation
4. Oversight
5. Study Description
Brief Summary
The purpose of this study was to evaluate the benefit of biventricular pacing in patients with heart failure who were receiving optimal pharmacological therapy, and who were either with or without an ICD indication
Detailed Description
Heart Failure is a syndrome that affects millions of patients in Europe with over half a million new cases reported annually. Drug therapy had been the conventional treatment of choice until the emergence of cardiac resynchronization therapy (CRT) where biventricular pacing can be delivered to the heart through a pacemaker or implantable cardioverter defibrillator. This study was designed to assess the effect of CRT on patients optimized on conventional heart failure medication including diuretics, beta blockers and ACE inhibitors. The effect of CRT was evaluated by comparison of 6 minute walk performance, Quality of Life and NHYA class after 6 months with CRT therapy either programmed ON or OFF. In addition, evaluation of the incidence of adverse events (predefined as ventricular arrhythmias, hospitalizations, drop-outs, complications and patient deaths) was done between groups at 6 months. Patients were all programmed ON after 6 months and data was collected for an additional 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Single
Allocation
Randomized
Enrollment
262 (false)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Contak heart failure devices
Primary Outcome Measure Information:
Title
Improvement in functional capacity as measured by a six-minute walk test at 6 months
Secondary Outcome Measure Information:
Title
Improvement in Quality of Life at 6 months; Improvement in NHYA classification at 6 months; incidence of adverse events at 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
- NYHA Class III and IV with EF < 35%; Optimal individual drug therapy in 2 weeks prior to enrollment including ACE inhibitors; beta blockers and diuretics unless not tolerated
Exclusion Criteria:
Reduced life expectancy of < 6 months or candidate for heart transplant within 6 months; chronic/recurrent atrial fibrillation/flutter
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
P HANRATH, MD
Organizational Affiliation
Medizinische Klinik I, University RWTH Aachen, Pauwelsstr. 30, 52057 Aachen, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guidant Corporation, , , Belgium
City
Diegem
ZIP/Postal Code
1831
Country
Belgium
Facility Name
Medizinische Klinik I, University RWTH Aachen
City
Aachen
ZIP/Postal Code
52057
Country
Germany
12. IPD Sharing Statement
Learn more about this trial
PACMAN - PAcing for CardioMyopathies, a EuropeAN Study
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