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Clinical Trials in Canada / NCT05650658
Recruiting Not applicable

Left vs Left Randomized Clinical Trial

NCT05650658 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2023-09-13
Last updated
2025-10-02

Condition(s) studied

Heart FailureHeart Failure With Reduced Ejection FractionAV BlockLBBBRBBBIntraventricular Conduction DelayPacing-Induced Cardiomyopathy

Investigational drug(s) / intervention(s)

His/LBBPBiVP

His/LBBP: Pacing at the level His-Bundle or left bundle branch is used to correct the underlying conduction abnormality, resulting in a faster and more homogeneous activation of the heart pacing directly via the intrinsic conduction system of the heart accompanied by a right atrial endocardial lead and a right ventricular defibrillator endocardial lead for LVEF≤35% and by a right atrial endocardial lead for LVEF 36-50%.

BiVP: Biventricular pacing has been shown to improve outcomes by delivering synchronized electrical stimuli to the right and left ventricles utilizing an an endocardial right atrial lead, an endocardial right ventricular lead, and an epicardial left ventricular lead implanted in a branch of the coronary sinus. For LVEF≤35% a biventricular pacemaker-defibrillator will be implanted while for LVEF 36-50% a biventricular pacemaker will be implanted.

Study summary

The investigators aim to prospectively test the comparative effectiveness of His or Left bundle branch pacing in relation to patient centered outcomes (quality of life, physical activity, heart failure hospitalization, mortality) and comparative safety in relation to device-related complications and re-interventions (e.g., lead dislodgement, infection) relative to standard of care biventricular pacing in patients with heart failure due to left ventricular systolic dysfunction (LVEF≤50%) and with either a wide QRS (≥130 ms) or with/anticipated \>40% pacing who are already receiving current standard heart failure pharmacological therapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Men and women 18 years of age or older. * A LVEF ≤ 50% within 6 months prior to enrollment. * Resting QRS duration ≥130 ms as evidenced by a historical 12-lead ECG prior to enrollment OR anticipated right ventricular pacing \>40% OR device in place with right ventricular pacing \> 40%. * Are optimized on HF guideline directed medical therapy according to current HF published guidelines OR patient's physician will make an effort to start all guideline-directed medical therapy and titrate doses up as permitted by the participant clinical status and co-morbidities prior to implantation procedure. Exclusion Criteria: * Women who are pregnant, lactating, or plan to become pregnant during the course of the trial. * Participants with angiographic evidence of coronary disease who are candidates for coronary revascularization and are likely to undergo coronary artery bypass graft surgery or percutaneous coronary, intervention in the next three (3) months. * Enzyme-positive myocardial infarction within the past three (3) months prior to enrollment. * Coronary artery bypass graft surgery or percutaneous coronary intervention (balloon and/or stent angioplasty) within the past three (3) months prior to enrollment. * Reversible non-ischemic cardiomyopathy (e.g., acute viral myocarditis). * Participants with Chagas disease, cardiac sarcoidosis or amyloidosis. * Expected to receive left ventricular assist device or heart transplantation within 6 months. * Participants with primary severe valvular disease (e.g., aortic stenosis). * Have a life expectancy of less than 12 months. * Participants with irreversible brain damage from preexisting cerebral disease. * Participants with a contrast dye allergy unable or unwilling to undergo pretreatment with steroids and/or diphenhydramine. * Participants participating in any other interventional cardiovascular clinical trial. * Participants who would be unable to comply with the study's follow-up visit schedule; or * Participants who had any prior unsuccessful attempt at implantation of biventricular pacing (BiVP), His Bundle Pacing (HBP), or Left Bundle Branch Pacing (LBBP) device.

Primary outcome measure(s)

Trial sites (71)

FacilityCityRegionStatus
Mercy Gilbert & Chandler Regional Medical Centers, Gilbert AZ Gilbert Arizona Recruiting
University of Arizona College of Medicine- Phoenix Tucson Arizona Recruiting
University of Arkansas for Medical Sciences (UAMS) Little Rock Arkansas Recruiting
University of California San Diego La Jolla California Recruiting
University of Colorado (Anschutz Medical Campus) Denver Colorado Recruiting
South Denver Cardiology Associates Littleton Colorado Recruiting
Hartford Hospital Hartford Connecticut Recruiting
Yale University New Haven Connecticut Recruiting
Heart Rhythm Solutions Davie Florida Recruiting
University of Florida Jacksonville Jacksonville Florida Not Yet Recruiting
Mount Sinai Medical Center of Florida, Inc. Miami Beach Florida Not Yet Recruiting
Cleveland Clinic Florida Palm Beach Gardens Florida Recruiting
Florida Heart and Vascular, LLC dba Florida Heart Rhythm Specialist, PLLC South Pasadena Florida Not Yet Recruiting
University of South Florida Tampa Florida Recruiting
Rush University Chicago Illinois Recruiting
University of Chicago Chicago Illinois Recruiting
Northwestern University Evanston Illinois Recruiting
CIS Clinical Research Corporation Naperville Illinois Enrolling By Invitation
Trustees of Indiana University Indianapolis Indiana Recruiting
Baptist Health Louisville Louisville Kentucky Recruiting
Massachusetts General Hospital Boston Massachusetts Recruiting
Beth Israel Deaconess Medical Center Boston Massachusetts Recruiting
Mayo Clinic Rochester Minnesota Recruiting
HMH Hospitals Corporation Hackensack New Jersey Recruiting
Virtua Health Marlton New Jersey Recruiting
Newark Beth Israel Medical Center Newark New Jersey Recruiting
The Valley Hospital, Inc. Ridgewood New Jersey Recruiting
Lovelace Medical Center Albuquerque New Mexico Recruiting
Weill Cornell Medicine New York New York Recruiting
Icahn School of Medicine at Mount Sinai New York New York Recruiting
Columbia University Medical Center/New York-Presbyterian Hospital (CUMC/NYPH) New York New York Not Yet Recruiting
MH Mission Hospital LLLP- Asheville Cardiology Associates Asheville North Carolina Recruiting
University of North Carolina Chapel Hill North Carolina Recruiting
Novant Health Charlotte North Carolina Recruiting
The Christ Hospital Cincinnati Ohio Recruiting
The MetroHealth System Cleveland Ohio Recruiting
Cleveland Clinic Cleveland Ohio Recruiting
Oregon Health & Science University Portland Oregon Recruiting
St. Luke's University Health Network Allentown Pennsylvania Recruiting
Lehigh Valley Hospital Inc. Allentown Pennsylvania Recruiting

+ 31 more sites — see the full list on the official registry below.

More Baylor College of Medicine trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05650658 on ClinicalTrials.gov ↗ ← All trials in Canada