Atrial Fibrillation Associated With Heart Failure Treated by BIOTRONIK's CRT-DX System
- Conditions
- Heart FailureAtrial FibrillationCardiac Resynchronization Therapy
- Interventions
- Device: CRT-DX
- Registration Number
- NCT04870281
- Lead Sponsor
- Biotronik, Inc.
- Brief Summary
The purpose of the BIO-AffectDX Study is to prospectively evaluate improvement from baseline in heart failure subjects with atrial fibrillation (AF) implanted with a two-lead CRT-DX system, with emphasis on a comparison of patient outcomes between AF subtypes.
- Detailed Description
There is a need for more evidence about the benefits of Cardiac Resynchronization Therapy (CRT) in a patient population with heart failure and atrial fibrillation. The BIO-AffectDX Study will gather information about adults with heart failure and atrial fibrillation who are treated with a CRT-DX device from many locations across the United States. The BIO-AffectDX Study will look at the results of treatment in participants with the primary goal to evaluate the improvement in overall health prior to device implant through 12 months. Overall health will be measured by your study doctor for AF improvement, physical fitness, and general quality of life.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 13
- Standard CRT-D indication according to current guidelines
- Patient has documented history of paroxysmal, persistent, or long-standing persistent atrial fibrillation
- De novo implant or upgrade from a DX implantable cardioverter-defibrillator (ICD) system
- Implant planned to occur within 30 days of consent
- Patient is able to understand English or Spanish
- Patient is able to understand the nature of the study and provide informed consent
- Patient is willing and able to complete all routine study visits at the investigational site for up to 12 months of follow-up
- Patient is willing to utilize BIOTRONIK Home Monitoring® via CardioMessenger
- Patient age is greater than or equal to 18 years
After consent has been signed, additional inclusion criteria must be fulfilled for study participation:
- Baseline subject assessment is evaluated as New York Heart Association class II, III or ambulatory IV heart failure at study Enrollment Visit
- Baseline subject assessment of six-minute walk test is completed at study Enrollment Visit and walk distance ≤ 450 meters (1,476 feet)
- Contraindication to CRT-D/CRT-DX
- Patient has current or previous atrial pacing need
- Patient is considered for a His Bundle Pacing system
- Patient has current or previous pacemaker, non-DX ICD implant, or bi-ventricular pacing system prior to enrolling
- Patient is currently planned for a pulmonary vein isolation catheter ablation procedure within 3 months of consent
- Patient life expectancy is less than 1 year
- Patient is expected to receive heart transplantation or ventricular assist device within 1 year after implant
- Patient is expected to have a cardiac surgical procedure, such as coronary artery bypass graft or valve transcatheter replacement/repair or surgery, planned to occur within 6-months after implant (excludes atrioventricular node ablation procedures)
- Patient is currently on dialysis, or is expected to receive dialysis within 1 year of implant
- Patient is enrolled in any investigational cardiac device or drug trial that might significantly affect the studied outcomes
- Any condition (e.g. severe arthritis, wheelchair bound, etc.) preventing the patient from performing the required six-minute walk test
- Conditions that prohibit placement of any of the system leads
- Patient reports pregnancy at the time of consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description CRT-DX System CRT-DX -
- Primary Outcome Measures
Name Time Method Change in Clinical Composite Score from baseline 12 months
- Secondary Outcome Measures
Name Time Method Change in six-minute walk distance from baseline for all patients and by atrial fibrillation sub-type 6 and 12 months Change in atrial fibrillation burden from baseline for all patients and by atrial fibrillation sub-type 6 and 12 months Change in quality of life questionnaires from baseline for all patients and by atrial fibrillation sub-type 6 and 12 months Rate of conversion to sinus rhythm 12 months Rate of composite all-cause death and heart failure 12 months Change in New York Heart Association class from baseline for all patients and by atrial fibrillation sub-type 6 and 12 months Change in Clinical Composite Score from baseline 6 months Rate of major complications 12 months
Trial Locations
- Locations (23)
Cardiology Associates Medical Group
🇺🇸Ventura, California, United States
AdventHealth Tampa
🇺🇸Tampa, Florida, United States
Glacier View Research Institute Cardiology
🇺🇸Kalispell, Montana, United States
Weill Cornell Medicine
🇺🇸New York, New York, United States
Cardiology Associates of North Mississippi
🇺🇸Tupelo, Mississippi, United States
Lenox Hill Hospital
🇺🇸New York, New York, United States
Michigan Heart
🇺🇸Ypsilanti, Michigan, United States
University of Kentucky - Gill Heart and Vascular Institute
🇺🇸Lexington, Kentucky, United States
Kansas City Heart Rhythm Institute
🇺🇸Overland Park, Kansas, United States
University of Michigan
🇺🇸Ann Arbor, Michigan, United States
Medical University of South Carolina
🇺🇸Charleston, South Carolina, United States
University of Cincinnati
🇺🇸Cincinnati, Ohio, United States
ProMedica Northwest Ohio Cardiology Consultants
🇺🇸Toledo, Ohio, United States
Massachusetts General Hospital
🇺🇸Boston, Massachusetts, United States
Upstate Cardiology
🇺🇸Greenville, South Carolina, United States
Mercy Hospital Springfield
🇺🇸Springfield, Missouri, United States
Heart Rhythm Associates
🇺🇸Greenville, North Carolina, United States
Erlanger Institute for Clinical Research
🇺🇸Chattanooga, Tennessee, United States
University of California San Diego - La Jolla
🇺🇸La Jolla, California, United States
Orlando Health Heart Institute
🇺🇸Orlando, Florida, United States
University of Iowa Hospitals and Clinics
🇺🇸Iowa City, Iowa, United States
Baptist Health Lexington
🇺🇸Lexington, Kentucky, United States
University of Kansas Medical Center
🇺🇸Kansas City, Kansas, United States