Clinical Trials Logo

Ventricular Premature Complexes clinical trials

View clinical trials related to Ventricular Premature Complexes.

Filter by:
  • Completed  
  • Page 1 ·  Next »

NCT ID: NCT05970120 Completed - Clinical trials for Ventricular Tachycardia

A Study of Intracardiac Ultrasound With the NUVISION NAV Ultrasound Catheter

Start date: September 5, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the performance and safety of using the investigational catheter.

NCT ID: NCT05373862 Completed - Clinical trials for Ventricular Tachycardia

A Study Assessing Arrhythmia Mapping With a Globe-Shaped, High-Density, Multi-Electrode Mapping Catheter

COSMOS
Start date: July 29, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the performance and safety for the use of the investigational catheter for intracardiac mapping in the atria and ventricles.

NCT ID: NCT05167058 Completed - Atrial Fibrillation Clinical Trials

Electrocardiographic Diagnostic Performance of the Apple Watch Augmented With an Artificial Intelligence Algorithm

Start date: April 21, 2022
Phase:
Study type: Observational

The SWAF study will compare the performance of a smartwatch combined with Cardiologs Platform algorithm in the detection of Atrial Fibrillation and other arrhythmias with that measured on a manually read 12-lead ECG in subjects hospitalized for cardioversion or AF ablation.

NCT ID: NCT05087238 Completed - Clinical trials for Ventricular Premature Complexes

CBT for Premature Ventricular Contractions

PVC-CBT
Start date: January 14, 2021
Phase: N/A
Study type: Interventional

The purpose of the present interdisciplinary research program is to develop and evaluate a disease-specific cognitive behavior therapy (CBT) protocol to increase quality of life (QoL) and reduce symptom burden in patients with Premature Ventricular Contractions (PVC).

NCT ID: NCT05008250 Completed - Clinical trials for Premature Ventricular Contraction

Efficacy and Safety of Metoprolol Tartrate Tablets Combined With Chinese Traditional Medicine on Premature Ventricular Complex.

Start date: January 2014
Phase: Phase 4
Study type: Interventional

Objective: investigators investigated the effects of metoprolol tartrate plus Tongmai Yangxin Pill on premature ventricular complexes and cardiac function in patients with premature ventricular complex. Methods: In total, 584 participants with premature ventricular complex will be randomly assigned (at a 1:1 ratio) into two groups: study group (metoprolol tartrate [25 mg twice per day, orally] plus Tongmai Yangxin Pill [40 pills twice per day, orally]) and control group (metoprolol tartrate [25 mg twice per day, orally] plus placebo [40 simulated pills twice per day, orally]). The total treatment period is 8 weeks. Efficacy endpoints and safety assessment: Primary efficacy endpoints are as follows: change in 24-h number of PVCs after treatment and effective rate of 24-h number of PVCs after treatment. Secondary efficacy endpoints are as follows: change in New York Heart Association classification; total effective rate of comprehensive effect; change in high-sensitivity C-reactive protein level; and change in echocardiography parameters (i.e., left ventricular ejection fraction, left ventricular end diastolic dimension, E/A, cardiac index, cardiac output, and stroke volume).

NCT ID: NCT04983797 Completed - Clinical trials for Paroxysmal Atrial Fibrillation

A Study Assessing Arrhythmia Mapping With the Multi-Electrode OPTRELL™ Mapping Catheter

OPTIMUM
Start date: August 25, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the performance and safety for the use of the OPTRELL Catheter for intracardiac mapping in the atria and ventricles.

NCT ID: NCT04884100 Completed - Atrial Fibrillation Clinical Trials

enHEART - Exploring Full Content of Optical Signals to Enhance Cardiac Arrhythmia Screening

enHEART
Start date: September 15, 2021
Phase: N/A
Study type: Interventional

This research will investigate the PPG signal morphology related to physiological and non- physiological changes in arrhythmia-related heart rate as well as the performance of the PPG-based features previously developed within the framework of the Mini-Holter study to discriminate between several cardiac arrhythmias. To this end, clinical data will be recorded on patients by using a wrist-based PPG monitor simultaneously with 12-lead ECG and intracardiac electrogram (EGM) signals at the university hospital in Lausanne. Importantly, this study will remain purely observational as it will not change the diagnostic and therapeutic management of the included patients, nor will it interfere with the time course of the procedures. The aim of enHEART study is to validate on a larger database the ability of several previously developed PPG-based features to detect a variety of cardiac arrhythmias.

NCT ID: NCT04559061 Completed - Atrial Fibrillation Clinical Trials

Vektor vMap™ Clinical Validation Study

Start date: December 1, 2020
Phase:
Study type: Observational

This is a retrospective, multi center clinical study collecting existing, de-identified subject data from medical records to be analyzed using an independent core laboratory to validate performance of a computational ECG mapping system (vMap™).

NCT ID: NCT04171479 Completed - Clinical trials for Ventricular Tachycardia

RMN Versus Manual Epicardial Retrospective PMCF

EPINAV
Start date: October 2, 2020
Phase:
Study type: Observational

Retrospective registry will compare subjects who've undergone a mapping and/or ablation procedure for either ischemic ventricular tachycardia or premature ventricular contraction using an epicardial approach with either manual or remote magnetic navigation. Subjects will be compared with regards to safety, efficacy and mortality.

NCT ID: NCT04065893 Completed - Clinical trials for Ventricular Tachycardia

Impact of Catheter Ablation of Ventricular Arrhythmias on Suboptimal Biventricular Pacing in Cardiac Resynchronization Therapy

Start date: September 1, 2020
Phase:
Study type: Observational

Cardiac resynchronization therapy reduces mortality in patients with systolic heart failure and left bundle branch block. Reduced biventricular pacing can lead to therapy failure. Most effective mortality reduction was seen with a BiV pacing above 98%. Reduced BiV pacing is a common phenomenon with potential impact on CRT-response and pts' prognosis. Frequent ventricular ectopy may be associated with attenuated benefit from CRT. The investigators sought to systematically assess the effect of ventricular arrhythmia treatment on BiV pacing.