Clinical Trials Logo

Arrhythmias, Cardiac clinical trials

View clinical trials related to Arrhythmias, Cardiac.

Filter by:

NCT ID: NCT03480204 Completed - Cardiac Arrhythmia Clinical Trials

Patient Status Engine (PSE): EARLY FEASIBILITY AND USABILITY STUDY

Start date: March 19, 2018
Phase:
Study type: Observational

This study evaluates the feasibility and usability of a wearable patch as a cardiac monitor for non-ICU hospitalized patients.

NCT ID: NCT03475888 Completed - Clinical trials for Chronic Total Occlusion of Coronary Artery

Incidence of Ventricular Arrhythmias in Patients With Chronic Total Occlusion Recanalization

VACTOR
Start date: September 28, 2018
Phase: N/A
Study type: Interventional

A chronic total occlusion (CTO) is common in patients with coronary artery disease. CTO recanalization has been shown to improve survival in comparison to failed CTO recanalization. Whether this is related to ventricular arrhythmias (VA) is unknown. The purpose of this pilot study is to evaluate the incidence of VA after successful CTO recanalization and in those with failed CTO recanalization or untreated CTO. Patients will be monitored using an insertable cardiac monitor.

NCT ID: NCT03461094 Completed - Arrhythmia Atrial Clinical Trials

Fluid Responsiveness Evaluation in Patients With Acute Circulatory Failure and Arrhythmia With Atrial Fibrillation: Indice Delta ITV / Delta RR

Start date: May 17, 2017
Phase: N/A
Study type: Interventional

Fluid therapy is often used as first line treatment of acute circulatory failure, aiming an increase in cardiac output (by improving preload) and in tissue perfusion. Depending on left ventricular systolic function, fluid challenge could lead to an increase in cardiac ouput and tissue perfusion, or only detrimental consequences (by fluid overload and aggravation of lung and tissues oedema, increase of morbi-mortality). Patients are defined as responders to fluid therapy if one can observe an increase of cardiac output up to 15% after fluid therapy (500ml of crystalloids): gold standard test used in most of the studies on the subject. Literature reports on heterogenous populations a reproductible and constant response rate to this fluid challenge of 50%. It seems reasonable to dispose of indices allowing to predict fluid responsiveness without resulting in fluid intake. Statics markers have been abandonned for several years and dynamics methods have been developped. In front of arrythmia, validated methods are scarce. Passive leg rising method appears to be the only one and it's validity seems to be less well documented than in sinusal patients. The purpose of this study is to determine a new method to assess fluid responsiveness in arrythmic patients. In atrial fibrillation, RR interval varies widely between cardiac cylces. Systolic interval remain constant. Variations will occure at expense of diastolic interval, or ventricular filling interval. One can reliably assume that when RR is longer, preload is rising. If the patient is on the ascendant part of the Franck-Starling curve, a longer RR should cause au greater VTI (Vitess Time Integral, surrogate of cardiac output). The evaluation by transthoracic echocardiography of the indice delta ITV / delta RR should determine the degree of fluid responsiveness in arrhythmic patients. After decision of fluid expansion, patients will have haemodynamic and echocardiographic data measured, delta ITV / delta RR indice assessed, then passive leg rising and fluid expansion with 500 ml of cristalloids administered, with evaluation of VTI (as surrogate of cardiac output) at each time. Fluid responders will be compared to non-responders to evaluate the diagnostic performances of the indice delta ITV / delta RR.

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: NCT03458273 Recruiting - Arrhythmia Clinical Trials

Real Zero Fluoroscopy Catheter Ablation.

ZERO-Fluoro
Start date: March 10, 2018
Phase:
Study type: Observational

A Retrospective Propensity Matched Study comparing: - real zero fluoroscopy catheter ablation - conventional fluoroscopy catheter ablation without 3D system - conventional fluoroscopy catheter ablation with 3D system

NCT ID: NCT03453931 Completed - Clinical trials for Corticosteroids Adverse Reaction

Arrhythmias, Microalbuminuria and Corticosteroids

Start date: January 10, 2018
Phase:
Study type: Observational

The goal of this observational design is to study the effects of intravenous corticosteroids on heart rate variability, arrhythmias and microalbuminuria. Some previous studies have shown that intravenous corticosteroids could induce bradycardia but also supra-ventricular tachycardia and atrial fibrillation. A second goal of this study is to investigate whether exogenous corticosteroids may induce microalbuminuria. A large retrospective study has revealed an association between microalbuminuria and corticosteroid use in the year preceding the measurement.

NCT ID: NCT03451721 Completed - Arrhythmia Clinical Trials

Observation of ImageReady™ MR Conditional Defibrillation System in China

Start date: April 3, 2018
Phase: N/A
Study type: Interventional

To observe the safety and effectiveness of ImageReady™ MR conditional defibrillation system in a Chinese population.

NCT ID: NCT03450226 Not yet recruiting - Cardiac Arrythmias Clinical Trials

Stellate Ganglion Block in Beating Heart Surgery

Start date: March 2018
Phase: N/A
Study type: Interventional

studies suggest that off-pump coronary artery bypass surgery is associated with improved outcomes when compared to on-pump coronary artery bypass. many studies have shown that off-pump coronary bypass surgery reduces patient morbidity and mortality. manipulation of the coronary arteries during cardiac surgery can stimulate the adjacent post-ganglionic sympathetic fibers and mimic stellate ganglion stimulation ,stellate ganglion block (SGB) can interrupt this reflex by decreasing the efferent cervical sympathetic outflows.

NCT ID: NCT03446794 Completed - Clinical trials for Cardiovascular Diseases

Left Atrial Appendage Occlusion With WATCHMAN® Device in Patients With Non-valvular Atrial Fibrillation and End-stage Chronic Kidney Disease on Hemodialysis

WATCH-HD
Start date: March 14, 2018
Phase:
Study type: Observational [Patient Registry]

Atrial fibrillation (AF) is more common in patients with renal disease compared to the general population an risk increase to as much as 10 times in patients on hemodialysis (HD). Stroke is an important cause of morbidity, mortality and suffering for patients with end-stage chronic kidney disease (ESCKD) on hemodialysis.The risk of bleeding in these patients can be roughly 5-fold higher that without it. Current guidelines recommend the use of oral anticoagulants (AO) to prevent stroke or systemic thromboembolism in high-risk patients with AF. Left atrial appendage occlusion (LAAO) reduces the risk of bleeding while allows thromboembolic stroke prevention. The aim of the study is to assess the procedural safety on stroke and bleeding prevention of LAAC in patients with non-valvular atrial fibrillation (NVAF) and ESCKD on HD.

NCT ID: NCT03444259 Active, not recruiting - Clinical trials for Coronary Artery Disease

Prospective Project to Identify Biomarkers of Morbidity and Mortality in Cardiovascular Interventional Patients

CAREBANK
Start date: February 1, 2016
Phase:
Study type: Observational [Patient Registry]

The objective of CAREBANK study is to establish definitive relationships with human cardiac samples and clinical phenotypes in patients undergoing cardiac procedures. Specifically, the investigators aim at comparing atrial phenotypes from atrial fibrillation patients and controls. The work consists of three broad categories: A) role of atrial cardiomyopathy in atrial fibrillation; B) genetic defects predisposing to atrial fibrillation; and C) the role of inflammation in atrial fibrillation.