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Ventricular Premature Complexes clinical trials

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NCT ID: NCT03671759 Completed - Clinical trials for Premature Ventricular Contractions

Coffee and Real-time Atrial and Ventricular Ectopy

CRAVE
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) and heart failure (HF) are morbid, costly, and incompletely understood diseases that have reached epidemic proportions worldwide. A dose-dependent relationship exists between premature atrial and ventricular contractions (PACs and PVCs) and development of AF and HF, respectively. Identifying and understanding the mechanisms of additional modifiable risk factors for ectopy has the potential to markedly reduce the healthcare burden of these diseases. In considering how to modify the prevalence of these ectopic beats, the investigators believe common exposures in daily life are prime candidates. Current guidelines suggest that caffeine may be an important trigger for frequent ectopy, although large population-based studies have not demonstrated an association between caffeine consumption and development of clinically significant arrhythmias. No study has employed an actual randomization intervention to assess the effects of caffeine on cardiac ectopy. Utilizing the Eureka platform, the investigators plan to utilize the N-of-1 strategy to rigorously investigate the real-time effect of caffeine intake on ectopy.

NCT ID: NCT03587558 Recruiting - Clinical trials for Ventricular Premature Complexes

Effects of Carvedilol on Suppressing the Premature Ventricular Complex/Ventricular Tachycardia From Outflow Tract

FOREVER
Start date: September 5, 2017
Phase: Phase 4
Study type: Interventional

Carvedilol is known to be effective in reducing ventricular arrhythmias and mortality in patients with heart failure. It is suggested that one of the mechanisms is its ability to block store overload-induced Calcium release which activates spontaneous calcium release by Ryanodine receptors. Ventricular outflow tract tachyarrhythmia is known to be associated with calcium overload due to activation of Ryanodine receptors. The aim of this study is to evaluate the efficacy of Carvedilol on premature ventricular complex(PVC)/ventricular tachycardia(VT) originating from outflow tract.

NCT ID: NCT03561935 Withdrawn - Clinical trials for Premature Ventricular Complex

Beta-blocker vs. Ic Antiarrhythmic Drug for PVC

Start date: June 2015
Phase: N/A
Study type: Interventional

The standard medical therapy of idiopathic premature ventricular complex consists of beta blocker and Ic antiarrhythmic agent. However, the difference in the efficacy of two drugs has not been well investigated. This prospective randomized study aimed to compare the efficacy of beta-blocker and Ic antiarrhythmic agent in the treatment of symptomatic patients with idiopathic premature ventricular complex.

NCT ID: NCT03460535 Recruiting - Cardiac Arrhythmia Clinical Trials

The Rhytmia System to Determine the Precise Location and Potential Mechanism of Premature Contractions

RhytmiaPVC
Start date: June 14, 2017
Phase: N/A
Study type: Observational

This is a purely observational project and the objectives are to record and analyze the local potentials at the site of Premature Ventricular Contraction (VPC) focus through the Rhythmia system, ti determine the short and long-term success of the procedure and compare it to the existing literature about standard procedures, to highlight the advantages of the system compared to conventional mapping and to characterize optimal pace map or activation map as achieved by the Rhythmia system.

NCT ID: NCT03447002 Completed - Clinical trials for Premature Ventricular Contraction

Urine Levels of Metanephrin and Normetanephrin in Patients With Frequent Ventricular Premature Complex

Start date: February 15, 2018
Phase:
Study type: Observational

Enhanced automaticity process is the underlying mechanism for arrhythmias due to excess catecholamines. Catecholamines may increase in patients with PVC. Metabolites of catecholamines are metanephrine and normetanephrine. Our aim is to measure 24 hours urine levels of metanephrine and normetanephrine.

NCT ID: NCT03418467 Recruiting - Atrial Fibrillation Clinical Trials

Risk Factors in Tachycardiomyopathy

EMPATHY
Start date: October 11, 2018
Phase:
Study type: Observational

Decision between rate control and rhythm control can be a challenge in clinical practice. While there is some guiding evidence, we still lack a comprehensive insight into different subgroups of patients that will benefit from a rhythm control treatment. EMPATHY is a prospective clinical study in patients presenting with heart failure and a tachyarrhythmic rhythm disturbance. Biomarkers, routinely obtained results from clinical examinations, and results from endomyocardial biopsies shall be evaluated to identify patients which have better outcome from a rhythm control strategy by ablation therapy or, if contraindicated by pharmacological rhythm control. This study is designed to identifying risk factors and subgroups profiting from rhythm restoration and therefore improve current therapeutic approaches and the rate of recurrence-free survival.

NCT ID: NCT03370679 Completed - Clinical trials for Premature Ventricular Contraction

The Prognostic Significance of Premature Ventricular Complexes in Patients Without Structural Heart Disease

PULSE
Start date: September 2013
Phase: N/A
Study type: Observational

With this project the investigators aim to investigate whether premature ventricular complexes (PVC) have a prognostic significance in persons without structural heart disease. Further the investigators look at the possible connection between PVC-morphology and clinical outcome and investigate whether advanced cardiac imaging-methods may identify subtle signs of heart disease in PVC-patients with normal findings at echocardiography.

NCT ID: NCT03365440 Completed - Atrial Fibrillation Clinical Trials

Esophageal 3D Mapping System for Cardiac Arrhythmias

esoECG-3D
Start date: December 15, 2017
Phase:
Study type: Observational

The aim of the study is to develop and validate a novel esophageal mapping system to improve the diagnostics of cardiac arrhythmias. Using a newly designed esophageal ECG catheter, esophageal ECGs (eECGs) will be recorded in 40 patients during an electrophysiological (EP) study and/or ablation procedure and in 12 healthy volunteers. In parallel acquired intracardiac electrograms will serve as reference for the developed mapping systems accuracy. Additionally, the esophageal mapping system will be compared to that of the standard 12-lead surface ECG in regard to its diagnostic performance.

NCT ID: NCT03340922 Completed - Catheter Ablation Clinical Trials

MANual vs. automatIC Local Activation Time Annotation for Guiding Premature Ventricular Complex Ablation

MANIaC-PVC
Start date: June 26, 2018
Phase: Phase 4
Study type: Interventional

Current navigation systems incorporate algorithms for automatic identification of local activation time (LAT). However, data about their utility and accuracy in premature ventricular complex (PVC) ablation procedures are scarce. This prospective, randomized study analyzes the accuracy and effectivity of an algorithmic method based on automatic annotation of the maximal negative slope of the unipolar electrogram within the window demarcated by the bipolar electrogram, compared with conventional, manual annotation during PVC ablation procedures.

NCT ID: NCT03340142 Completed - Clinical trials for Ventricular Tachycardia

VIVO™ Accuracy Study

Start date: January 29, 2018
Phase: N/A
Study type: Interventional

A multi-center study designed to assess the accuracy of VIVO™ in determining the location of a PVC/VT foci in comparison to an electroanatomical mapping system.