Pacemaker Ddd

6

Review clinical trials related to Pacemaker Ddd. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Conduction System Pacing With Left Bundle Branch Pacing as Compared to Standard Right Ventricular Pacing

High burden right ventricular (RV) pacing has been shown to increase cardiovascular mortality, incidence of heart failure (HF), worsen left ventricular (LV) function and accelerate the development of atrial fibrillation (AF). High percentage ventricular pacing and wider paced QRS in the setting of normal baseline LV ejection fractions have consistently been shown to be independent risk factors for pacing-induced cardiomyopathy. Left bundle branch pacing (LBBP) has emerged as a potential alternative pacing mechanism that may avoid LV dyssynchrony and pacing-induced LV dysfunction by mimicking native electrical conduction.

Participants needed: 1,300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: McGill University Health Centre/Research Institute of the McGill University Health CentreUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years [+5]

Indication for an implantable cardioverter defibrillator [+7]

Status: Recruiting

Remote Alert Pathway To Optimize CaRe of Cardiac Implantable Electrical Devices

The Remote Alert Pathway to Optimize Care of Cardiac Implantable Electrical Devices (RAPTOR-CIED) Study is a pragmatic, multi-center, randomized trial with 1:1 patient-level randomization comparing the safety and effectiveness of alert-driven care versus guideline-based care for patients with wireless cardiac implantable electrical devices (CIEDs). The study will be conducted in 2 phases: a Feasibility Phase and a Main Phase. This registration outlines the goals and design features of the Feasibility Phase of the study.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Beth Israel Deaconess Medical CenterUpdated: Jan 7, 2026Locations: 1
Eligibility criteria

Adult aged > 18 years [+7]

Presence of insertable cardiac monitor, either in isolation or in combination wi... [+2]

Status: Recruiting

Left Bundle Branch Area Mapping for Conduction System Pacing

This study will utilize 3D mapping as a tool to explore electro-anatomical and electrocardiographic characteristics of the Left Bundle Branch Area. We plan on prospectively reviewing the data found from 3D mapping the left bundle branch implantation cases and using the data to improve understanding of electro-anatomical characteristics of this area for a better definition of the implantation target and depth.

Participants needed: 30
Trial details
Age: 18-88Biological sex: AllType: ObservationalSponsor: Steward St. Elizabeth's Medical Center of Boston, Inc.Updated: Dec 17, 2025Locations: 1
Eligibility criteria

30 consecutive patients ages 18 through 88 that undergo Left Bundle Branch area...

Recent MI-less than 3 months [+3]

Status: Recruiting

Non-Invasive Method for Evaluation of Cardiac Resynchronization Therapy

Left bundle branch block (LBBB) exists in about 25% of patients with congestive heart failure and is associated with worsened prognosis. Cardiac resynchronization therapy (CRT) has been one of the most important advancements in the past two decades for patients with LBBB heart failure. However, 30-40% of patients receiving a CRT do not benefit from it. In this study, the investigators will test a noninvasive device to evaluate acute effect of CRT during implantation and at follow-up CRT controls. In addition, echocardiography will be performed during CRT turned ON and OFF to visualize the changes in intraventricular flow and functional parameters of the heart.

Participants needed: 80
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Oslo University HospitalUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Sinus rhythm. [+6]

Age < 18 years and > 80 years; [+2]

Status: Recruiting

Prospective Database for Prediction of Atrial Fibrillation in Pacemaker and ICD Patients

Atrial fibrillation (AF) is associated with a five-fold increased risk of cerebrovascular stroke. While the risk of stroke in patients with known AF can be calculated via AF stroke prediction risk scores, the prediction of AF occurrence per se in individual patients remains difficult. We will recruit 250 patients with an implanted dual-chamber Pacemaker (PM) or an implantable cardioverter Defibrillator (ICD) with atrial lead to ensure continuous rhythm monitoring during follow up. At baseline, we will gather clinical and device data of patients. For AF prediction based on surface Electrocardiography (ECG), 24-h Holter ECG monitoring will be performed. After 6 months, we will assess the occurrence of AF during the study period via interrogation of PM/ICD. The resulting data will be used to develop algorithms including clinical, device and ECG data for prediction of the development of AF in individual patients. If possible, we will develop a risk score of high accuracy by combination of demographical, clinical and technical parameters of device patients. The resulting risk score could potentially help to facilitate the decision if anticoagulation is necessary in patients with either risk of AF or embolic stroke of unknown origin. Furthermore, Hayn et al. (AIT Austrian Institute of Technology) are currently developing algorithms to predict the occurrence of AF surface ECG data. It is an additional aim of this project to support the development of this algorithm in pacemaker and ICD patients and to increase the accuracy of AF prediction with clinical parameters and other parameters available to patients with implanted pacemaker (PM) or implanted cardioverter-defibrillator (ICD).

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Medical University of GrazUpdated: Nov 21, 2024Locations: 1
Eligibility criteria

Implanted pacemaker or implanted cardioverter defibrillator (ICD) with atrial le... [+4]

pacemaker or ICD malfunction [+3]

Status: Recruiting

Pacing to Maintain Physiologic Ventricular Activation

Right ventricular pacing causes ventricular dyssynchrony and may be associated with impaired outcome. In the last decade, several approaches for more physiological pacing became available and were implemented in the latest guidelines. However, compared to conventional device implantation, cardiac resynchronization, His bundle pacing and left bundle area pacing remain demanding procedures in the individual case. Goal of the single center observational "Pace conduct" study is to evaluate implantation success, safety and outcome of pacing methods that maintain physiologic ventricular activation.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Klinikum-FuerthUpdated: Oct 15, 2024Locations: 1Duration: 1 Year
Eligibility criteria

Pacemaker or ICD Implantation aiming to avoid pacing induced ventricular dyssync... [+1]

no informed consent for the procedure given [+1]