High Intensity His Bundle Pacing in Heart Failure Patients With Narrow QRS Outcome Study
Condition(s) studied
Investigational drug(s) / intervention(s)
High Intensity His Bundle pacing: All patients will be implanted with an Implantable cardioverter defibrillator (ICD) and an ICD lead in the right ventricle (either RV apex or RV septum). In all patients a pacing lead will be positioned in the right atrium (typically the right atrial appendage). All patients will have a pacemaker lead positioned on the His bundle to obtain direct His-bundle capture.
Study summary
Cardiac Resynchronization Therapy (CRT) decreases heart failure hospitalizations and mortality and increases left ventricular Ejection Fraction (EF) in patients with dilated cardiomyopathy, left bundle branch block and QRS duration \>130msec. His bundle pacing has a similar effect in this category of patients. However, CRT is not beneficial in heart failure (HF) patients with narrow QRS. His-bundle pacing delivers physiological ventricular activation and has been shown to improve acute hemodynamic function in patients with heart failure, a prolonged PR interval, and either a narrow QRS or RBBB through AV delay optimization. We observed an acute hemodynamic effect during application of higher pacing output (3.5 Volts/1 msec) in HF patients with dilated or ischemic cardiomyopathy and narrow QRS independently of the paced QRS duration or AV delay shortening.
This is a single-center, prospective randomized single-blinded study, recruiting a sub-population of patients with heart failure (dilated or ischemic cardiomyopathy, EF\<50%, narrow QRS (\<110 msec), in optimal medical treatment who have an indication for ICD.
Eligibility
Primary outcome measure(s)
- Change in left ventricular ejection fraction — Baseline pre-intervention, randomisation and 6 months post randomisation
change in left ventricular ejection fraction measured by 2D echo at 6 months compared to baseline
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Miulli General Hospital | Acquaviva delle Fonti | Bari | Recruiting |
Other trials for the same condition
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 NCT05491655 on ClinicalTrials.gov ↗ ← All trials in Italy