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Ventricular Premature Complexes clinical trials

View clinical trials related to Ventricular Premature Complexes.

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NCT ID: NCT03288766 Terminated - Atrial Flutter Clinical Trials

SHERLOCK 3CG™ Diamond Tip Confirmation System

MODUS II
Start date: April 19, 2018
Phase:
Study type: Observational

This study is a single-arm, prospective, multi-center study to assess clinical performance of the SHERLOCK 3CG™ Diamond Tip Confirmation System (TCS) with MODUS II software for confirming correct tip position of peripherally inserted central catheters (PICCs) in adult subjects with altered cardiac rhythm.

NCT ID: NCT03249545 Recruiting - Ablation Clinical Trials

Late Effect of Ablation on Premature Ventricular Complex Ablation

Start date: July 1, 2017
Phase: N/A
Study type: Observational

Premature Ventricular Complex (PVC) ablation is performed in certain indications. Generally acutely abolition of PVC at the time of ablation accepted as successful ablation. However in some patients this effect occurs lately. In this study investigators sought late effect of ablation

NCT ID: NCT03228823 Active, not recruiting - Cardiomyopathies Clinical Trials

Prospective Assessment of Premature Ventricular Contractions Suppression in Cardiomyopathy(PAPS)

PAPS
Start date: August 1, 2018
Phase: Phase 4
Study type: Interventional

Premature ventricular contractions (PVCs) coexist in patients with heart failure (HF) and LV dysfunction. Frequent PVCs have shown to induce a reversible cardiomyopathy (PVC-CM). This clinical pilot study will enroll 36 patients with frequent PVCs (burden >10%) and CM (LVEF <45%) and randomize them to either: 1) RFA or 2) AADs. Prior to treatment, patients will undergo a baseline cardiac MR if clinically indicated followed by 3-month observation period (optimal HF medical therapy). Changes in LV function/scar, PVC burden/arrhythmias and clinical/functional status (QOL, HF symptoms and admissions, NYHA class) and adverse events will be assessed throughout the observation period and compare with PVC suppression strategies (RFA or AAD). Similar comparison will be made between RFA and AAD treatment groups during a 12-month follow up using a Prospective Randomized Open, Blinded End-point (PROBE) study design. The treatment regimens will be compared in an intention-to-treat analysis. In addition, a total of 20,000 consecutive ambulatory ECG Holter monitors from all participating centers will be screened to identify all patients with probable diagnosis of PVC-CM. This pilot study is intended to estimate the prevalence of this clinical entity and pave the way for a large full scale randomized trial to identify best treatment strategy for patients with PVC-CM. Treating and reversing this underestimated PVC-CM may improve patient's health and subsequently decrease HF healthcare spending.

NCT ID: NCT03218137 Recruiting - Clinical trials for Premature Ventricular Contraction (PVC)

Use of Adenosine to Determine the Electrophysiological Mechanism of Premature Ventricular Contractions

Start date: February 13, 2017
Phase: Phase 4
Study type: Interventional

Unblinded, controlled, non-randomized, mechanistic study to determine whether physiological mechanisms underlying PVC are sensitive to adenosine. One hundred subjects undergoing clinically-indicated, standard-of-care cardiac electrophysiology study (EPS) procedure for PVCs will receive adenosine and/or verapamil to learn if their arrhythmias are inducible similarly to sustained ventricular tachycardia.

NCT ID: NCT03086902 Not yet recruiting - Clinical trials for Premature Ventricular Contraction

Comparision of PVC Ablation Techniques

PVC
Start date: December 2018
Phase: N/A
Study type: Interventional

Several reports have shown the utility of PVC ablation with cryo catheters. The aim of this study is to compare the outcomes and safety of Cryo vs. RF for PVCs.

NCT ID: NCT03041519 Recruiting - Clinical trials for Ventricular Tachycardia

Zero-fluoroscopic Ablation Versus Conventional Fluoroscopic Ablation for the Treatment of Ventricular Arrhythmias

ZFOVA
Start date: October 2011
Phase: N/A
Study type: Interventional

This study is intended to compare the feasibility, safety and efficacy of a zero-fluoroscopy approach using Ensite NavX as the only imaging modality with conventional fluoroscopic approach for the catheter ablation of idiopathic ventricular arrhythmias; conventional fluoroscopic approach use fluoroscopy plus Ensite NavX or plus Carto as the imaging modality.

NCT ID: NCT02924285 Completed - Heart Diseases Clinical Trials

Catheter Ablation Versus Amiodarone for Therapy of Premature Ventricular Contractions in Patients With Structural Heart Disease

CAT-PVC
Start date: November 1, 2017
Phase: Phase 3
Study type: Interventional

For therapy of symptomatic premature ventricular complexes (PVCs) in subjects with structural heart disease the current European Guidelines for the management of patients with ventricular arrhythmias and the prevention of second cardiac death recommend catheter ablation as well as amiodarone with a class IIa indication. Due to the lack of randomized data this study investigates the comparison of catheter ablation and amiodarone for PVC treatment in patients with structural heart disease. Therefore, patients will be randomized to one of two treatment strategies: 1) catheter ablation, or 2) amiodarone.

NCT ID: NCT02919618 Active, not recruiting - Clinical trials for Ventricular Tachycardia

Phase I/II Study of EP-guided Noninvasive Cardiac Radioablation for Treatment of Ventricular Tachycardia

ENCORE-VT
Start date: July 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Phase I/II Study of EP-guided Noninvasive Cardiac Radioablation (ENCORE) for Treatment of Ventricular Tachycardia

NCT ID: NCT02772354 Recruiting - Clinical trials for Ventricular Arrhythmia

Radiofrequency Ablation of Symptomatic Frequent Ventricular Premature Complexes in Pediatric Population

RAS
Start date: April 2016
Phase: Phase 2/Phase 3
Study type: Interventional

To evaluate the effectiveness and safety of catheter ablation of frequent symptomatic PVCs in the pediatric population as first-line therapy compared with antiarrhythmic drugs.

NCT ID: NCT02666742 Completed - Stroke Clinical Trials

DOACs for Stroke Prevention Post Ventricular Tachycardia Ablation

STROKE-VT
Start date: February 16, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to learn if taking a drug called direct oral anticoagulant after an ablation procedure keeps blood clots from forming and lowers the chance of having a stroke in patients with ventricular tachycardia or arrhythmia (VT).