Ireland
--:--IST
Recruiting Not applicable

RandomIsed sTudy of Physiologic cArdiac stimuLation in patIents With Atrio-ventricular Conduction Disease

NCT07279870 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2025-12-03
Last updated
2026-05-27

Condition(s) studied

Atrioventricular Block

Investigational drug(s) / intervention(s)

Conduction System Pacing (CSP)Right Ventricular (RV) Pacing

Conduction System Pacing (CSP): CSP occurs at the left endocardic surface of the interventricular septum hence specifically designed delivery catheters are used to advance the ventricular lead across the septum until its left-sided edge, where the Left Bundle is located. To determine whether CSP has been achieved, a standard 12-lead electrocardiogram (ECG) is continuously recorded.

Right Ventricular (RV) Pacing: RV pacing delivered either at the RV apex or RV septum. RV pacing is delivered by single chamber or dual chamber pacemakers depending on patients' rhythm (sinus or AT/AF) according to well-established clinical practice as described in the EHRA recommendtions

Study summary

Study objective is to assess whether stimulation of the conduction system reduces cardiac decompensation events in patient follow-up, and how applicable this is in clinical practice and also to determine the impact of the studied interventions in terms of quality of life and cost-effectiveness for the treatment of patients with atrioventricular block. 1260 adult patients who are candidates for pacemaker implantation for the treatment of atrioventricular conduction disease will be randomised to stimulation of the conduction system or to the conventional stimulation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients with AV block in either sinus rhythm (SR) or permanent atrial tachycardia/atrial fibrillation (AT/AF), or with slow AV conduction during AT/AF, or undergoing AV node ablation + ventricular stimulation * male and female * acquired informed consent Exclusion Criteria: * Class I indication to Implantable Cardioverter Defibrillator (ICD) or to Cardiac Resynchronization Therapy (CRT) * Ejection Fraction \< 35% * Life expectancy \< 2 years * Participation in another clinical trial which might impact on the study outcome * Pregnancy, except as "In the event of an ongoing pregnancy, the doctor and patient will jointly assess, on a case-by-case basis and in the best interests of the patient, whether to propose participation in the study (random assignment to one of the two stimulation techniques) or to proceed as per clinical practice (assignment to one of the two stimulation techniques by the doctor). A screening log file of all eligible patients will be recorded, detailing the reason/s for non-randomization."

Primary outcome measure(s)

  • Heart failure — 36 months after the PM implant
    composite endponit of: number of HF events, HF hospitalizations and HF non-pharmacological interventions

Trial sites (14)

FacilityCityRegionStatus
Azienda Ospedal iera "Card. G. Panico" Bari Italy Not Yet Recruiting
IRCCS AOUBO Policlinico di Sant'orsola Bologna Italy Recruiting
Azienda Ospedaliero-Universitaria Policlinico "G. Rodolico -San Marco" Catania Italy Not Yet Recruiting
Azienda Ospedaliero-Universitaria di Ferrara Ferrara Italy Recruiting
ASST Grande Ospedale Metropolitano Niguarda Milan Italy Not Yet Recruiting
Azienda Ospedaliero-Universitaria Maggiore della Carità di Novara Novara Italy Not Yet Recruiting
Azienda Sanitaria locali di Asti Ospedale Cardinal Massaia Novara Italy Not Yet Recruiting
Azienda Ospedaliero-Univeritaria di Palermo - Policlinico Giaccone Palermo Italy Not Yet Recruiting
Azienda Ospedaliero-Universitaria di Parma Parma Italy Not Yet Recruiting
Azienda Ospedaliera Santa Maria della Misericordia Perugia Italy Not Yet Recruiting
Policlinico Casilino Roma Italy Not Yet Recruiting
Ospedale di Rovigo Aulss 5 Polesana Rovigo Italy Not Yet Recruiting
Città delle Salute e della Scienza di Torino. Dipartimento Cardiovascolare e Toracico Torino Italy Not Yet Recruiting
APSS Trento - Ospedale S. Maria del Carmine di Rovereto Trento Italy Not Yet Recruiting
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 NCT07279870 on ClinicalTrials.gov ↗ ← All trials in Italy