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Left Bundle Branch Area Pacing in Heart Failure Patients With Ejection Fraction Below Normal

Left Bundle Branch Area Pacing in Heart Failure Patients With Ejection Fraction Below Normal

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06148571
Enrollment
142
Registered
2023-11-28
Start date
2023-10-10
Completion date
2026-07-03
Last updated
2026-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Left Ventricular Ejection Fraction Less Then or Equal to 50percent

Brief summary

While cardiac resynchronization therapy remains the mainstay for advanced HF, it is not always feasible due to unfavorable anatomy of coronary sinus or pacing characteristics. In such cases, left bundle branch area pacing itself or left bundle optimized cardiac resynchronization therapy could be a rescue therapy for failed or unsuccessful biventricular cardiac resynchronization therapy. However, the efficacy and safety of left bundle branch area pacing (or left bundle optimized cardiac resynchronization therapy) as rescue therapy for biventricular cardiac resynchronization therapy is largely hypothetic and lack concrete evidence still. Therefore, there is an unmet need for the registry purposed for left bundle branch area pacing among heart failure with mid-range (or mildly reduced) ejection fraction and heart failure with reduced ejection fraction patients to investigate its efficacy and safety. This study aims to investigate the efficacy and safety of left bundle branch area pacing in heart failure patients with ejection fraction below normal using Selectra catheters.

Interventions

DEVICEleft bundle branch area pacing

left bundle branch area pacing locates ventricular lead into the interventricular septum to capture left bundle branch areas.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients previously diagnosed with heart failure with mid-range(or mildly reduced) ejection fraction and heart failure with reduced ejection fraction, which was documented by an appropriate echocardiographic study (Left ventricle ejection fraction \<50%), and * Patients with indications of cardiac pacing or cardiac resynchronization therapy

Exclusion criteria

* Patients aged less than 19 years. * Pregnant. * Patients with an expected life expectancy of less than 1 year. * Patients with a mechanical valve for the tricuspid valve. * Patients who need atrial pacing only. * Patients who are not capable of receiving a transvenous pacemaker for any reason.

Design outcomes

Primary

MeasureTime frameDescription
The acute success rate of left bundle branch area pacingThe day of the procedureThe acute success of left bundle branch area pacing was defined as below: Meet ≥2 criteria as follows evaluated at the end of the procedure. * Right bundle branch block configuration observed during unipolar tip pacing * Left bundle branch potential (Left bundle branch-Ventricular interval of 15 to 35ms) * Transition from nonselective Left bundle branch capture to selective Left bundle branch capture * Transition from nonselective Left bundle branch capture to left septal capture at near threshold outputs * Short and constant peak left ventricular activation time (stimulus to peak of the R wave in V5 or V6 \[peak left ventricle activation time\]) \<75ms in non-Left bundle branch block and \<85ms in Left bundle branch block Programmed (extra-stimulus testing) deep septal stimulation to differentiate left ventricular septal vs nonselective Left bundle branch capture
Acute complications related to the procedures7 days from the procedure* Death related to the procedure * Vascular complications (pocket hematoma, pseudoaneurysm, fistular, rupture) * Device-related infection * Cardiac perforation or tamponade * Septal perforation * Acute coronary syndrome * Pneumothorax, hemothorax * Thromboembolic events (stroke, pulmonary thromboembolism) * Lead dislodgment

Secondary

MeasureTime frameDescription
The incidence of acute procedure-related complication1 yearThe acute procedure-related complication was defined as the occurrence of the below-listed events within 7 days of the procedure. (Death related to the procedure, Pocket hematoma, Pseudoaneurysm, Fistular, Vascular rupture, Device-related infection, Cardiac perforation, Cardiac tamponade, Septal perforation, Acute coronary syndrome, Pneumothorax, Hemothorax, Stroke, Pulmonary thromboembolism, Lead dislodgement)
The incidence of repeat procedures1 yearThe incidence of repeat left bundle branch area pacing procedures
The incidence of pacemaker upgrade to cardiac resynchronization therapy including biventricular cardiac pacing1 yearThe incidence of pacemaker upgrade to cardiac resynchronization therapy including biventricular cardiac pacing
The incidence of heart failure hospitalization1 yearThe incidence of heart failure hospitalization
The incidence of cardiovascular death1 yearThe incidence of cardiovascular death
The incidence of All-cause death1 yearThe incidence of All-cause death
Left ventricular ejection fraction1 yearLeft ventricular ejection fraction (%)
Left ventricular end diastolic diameter1 yearLeft ventricular end diastolic diameter (mm)
Left ventricular end systolic diameter1 yearLeft ventricular end systolic diameter (mm)
left ventricular global strain1 yearleft ventricular global strain (%) if possible.
Capture threshold1 yearLeft bundle branch area pacing lead parameter: capture threshold (V)
Sensing1 yearLeft bundle branch area pacing lead parameter: sensing (mV)
Impedance1 yearLeft bundle branch area pacing lead parameter: impedance (Ohms)

Countries

South Korea

Contacts

PRINCIPAL_INVESTIGATOREue-Keun Choi, M.D. Ph.D.

Seoul National University Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026