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Safety and Effectiveness of Left Bundle Branch Area Pacing Versus Conventional Cardiac Resynchronization Therapy in Heart Failure
NCT07069738 · View on ClinicalTrials.gov ↗
Study Summary
This study will compare two different methods to pace the heart to treat heart failure including: 1. The current standard method of implanting a pacing lead in a vein on the surface of the left lower chamber of the heart (left ventricle) to deliver heart failure therapy. This method is called Cardiac Resynchronization Therapy (CRT). 2. The other method is using a lead implanted in the Left Bundle Branch Area (LBBA) of your heart. This method is called Left Bundle Branch Area Pacing or LBBAP. This lead is approved by the Food and Drug Administration (FDA) to be implanted in this area of the heart, but not to provide heart failure treatment.
Conditions Studied
Interventions
- DEVICE CRT-D with a Quadripolar LV lead
- DEVICE CRT-D with INGEVITY+ pace/sense lead
Study Locations (18)
New York
- New York Hospital Queens — Flushing
- Weill Cornell Medical University — New York
- Rochester General Hospital — New York
Alabama
- Heart Center Research, LLC — Huntsville
- Mobile Infirmary Medical Center — Mobile
California
- Alta Bates Summit Medical Center — Oakland
- Cardiology Associates Medical Group, Inc. — Ventura
Minnesota
- St. Mary's Duluth Clinic Regional Heart Center — Duluth
- Centracare Heart and Vascular Center — Saint Cloud
Arkansas
- Arrhythmia Research Group — Jonesboro
Florida
- Sarasota Memorial Hospital — Sarasota
Georgia
- Emory University Hospital — Atlanta
Illinois
- Midwest Cardiovascular Institute — Naperville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 850 participants |
| Start Date | 2025-10-22 |
| Est. Completion | 2029-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07069738
The ClinicalTrials.gov registry entry for NCT07069738 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 850 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Scientific Corporation, which has 120 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Heart Failure - NYHA II - IV appearing as the primary indexed condition, and to 2 interventions — of which CRT-D with a Quadripolar LV lead is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07069738 reports 18 study locations spanning 13 distinct geographic areas — top geographies include New York, Alabama, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07069738 about?
NCT07069738 is a clinical study titled "Safety and Effectiveness of Left Bundle Branch Area Pacing Versus Conventional Cardiac Resynchronization Therapy in Heart Failure". This study will compare two different methods to pace the heart to treat heart failure including: 1. The current standard method of implanting a pacing lead in a vein on the surface of the left lower chamber of the heart (left ventricle) to deliver heart failure therapy. This method is called Cardi...
What is the current status of trial NCT07069738?
This trial is currently recruiting. It is a NA study. The enrollment target is 850 participants. The study started on 2025-10-22. Estimated completion is 2029-11.
What conditions does trial NCT07069738 study?
This clinical trial studies the following conditions: Heart Failure - NYHA II - IV. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07069738?
The interventions under investigation include: CRT-D with a Quadripolar LV lead (DEVICE), CRT-D with INGEVITY+ pace/sense lead (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07069738?
This trial is sponsored by Boston Scientific Corporation, which has 120 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07069738 being conducted?
This trial has 18 study locations across Alabama, Arkansas, California, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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