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Arrhythmias clinical trials

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NCT ID: NCT02565069 Completed - Arrhythmias Clinical Trials

Identification for the Treatment of Complex Arrhythmias

Start date: July 1, 2015
Phase: Phase 4
Study type: Interventional

The primary purpose of this trial is to demonstrate that the utilization of CartoFinder™ 4D Local Activation Time (LAT) Algorithm may help identify and improve the outcome for the treatment of complex arrhythmias.

NCT ID: NCT02110004 Completed - Arrhythmias Clinical Trials

Picasso NAV High-Density Mapping Catheter for Signal Analysis of Complex Arrhythmias - First-In-Man

Start date: March 2014
Phase: Phase 1
Study type: Interventional

The primary purpose of the First-In-Man clinical investigation is to assess the Picasso NAV Catheter's ability to collect intracardiac signals within the desired chambers (atrial and/or ventricle) in the heart for the analysis of complex arrhythmias.

NCT ID: NCT02045173 Completed - Sleep Apnea Clinical Trials

Automate Detection of Sleep Apnea by ApneascanTM

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

The purpose of the study is to compare, three months after implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy-defibrillator (CRT-D), the apnea-hypopnea index (AHI) obtained from conventional in-lab NPSG/NPG (AHIPSG) with similar indices obtained from autoscoring algorithms of the ApneaScan™, an implantable impedance-based respiration sensor (AHIAS).

NCT ID: NCT02045043 Completed - Clinical trials for Congestive Heart Failure

Genetic Risk Assessment of Defibrillator Events

GRADE
Start date: March 2002
Phase: N/A
Study type: Observational

Arrhythmias remain a major health problem, causing at least 250,000 deaths annually in the United States. Pharmacological treatments often do more harm than good, and device therapies are limited by high cost and effects on quality of life. Ion channel mutations cause rare inherited arrhythmopathies, but account for only a small fraction of patients with life- threatening arrhythmias and sudden death. Most arrhythmias occur during myocardial ischemia, following myocardial infarction, and in patients with poor left ventricular (LV) function of any etiology. Aside from ejection fraction (EF), few clinically useful indicators to stratify the risk of sudden death have been identified. The role of subtle difference in ion channel expression and/or structure in predisposing patients to arrhythmias and modulating the risk of sudden death is unknown. In this study, we are prospectively testing whether polymorphisms in ion channels and ion channel modifying genes are associated with arrhythmias in a population with internal cardioverter-defibrillators (ICDs) and poor LV function. We will test the hypothesis that functional polymorphisms in the coding sequences and promoter regions of cardiac genes (e.g. ion channels, beta-adrenergic receptors) predispose individuals to arrhythmias and /or heart failure progression. We hope to identify genetic predictors for the common forms of sudden cardiac death. This would allow the identification of a subpopulation of heart failure patients that would benefit most from ICD placement.

NCT ID: NCT01834872 Unknown status - Arrhythmias Clinical Trials

Safety and Feasibility of Arrhythmia Ablation Using the Amigo Remote Robotic System as Compared With Manual Ablation

Start date: September 2012
Phase: Phase 4
Study type: Interventional

The aim of this prospective observational study is to evaluate the performance of Amigo RCS in ablation procedures for most common arrhythmias as compared to a conventional manual approach.

NCT ID: NCT01819064 Completed - Bradycardia Clinical Trials

Heart Rate Response to Atropine Doses Less Than 0.1mg IV to Anesthetized Infants

Start date: February 2013
Phase: Phase 4
Study type: Interventional

An infants heart rate is very important because it ensures that blood is pumped to all organs in the body. Heart rate may decrease during anesthesia and surgery, and this is why the anesthesiologist will often give a medication to prevent this from happening. The most common drug for this purpose is called atropine. The dose of most drugs given to babies is based upon the baby's weight, but some believe that the dose of atropine should not be less than 0.1mg. However there is no evidence to support this minimum dose. A larger dose of atropine may cause a very fast heart rate instead. Anesthesiologists routinely dose the atropine based upon the baby's weight without regard for a minimum dose. The purpose of the present study is to measure the heart rate after doses of atropine in neonates and infants who receive less than 0.1 mg.

NCT ID: NCT01717495 Recruiting - Clinical trials for Cardiovascular Disease

Thromboembolic Complications After Pacemaker or Implantable Cardioverter-Defibrillator Procedures

Start date: April 2013
Phase: N/A
Study type: Observational

This is a large prospective registry of patients submitted to cardiac electronic devices implantation designed to investigate the incidence, risk factors and prognostic of thromboembolic complications associated with transvenous lead implantation.

NCT ID: NCT01717469 Recruiting - Clinical trials for Cardiovascular Disease

Safety and the Effects of Isolated Left Ventricular Pacing in Patients With Bradyarrhythmias

SAFE-LVPACE
Start date: June 2012
Phase: Phase 4
Study type: Interventional

Previous experimental and clinical studies have consistently suggested that right ventricular (RV) apical pacing has important adverse effects. Ventricular pacing, however, is required, and cannot be reduced in many patients with atrioventricular block. The SAFE-LVPACE study is a randomized controlled trial that compare the effects of conventional right ventricular (RV) pacing vs. left ventricular (LV) in patients with AV block.

NCT ID: NCT01651702 Withdrawn - Arrhythmias Clinical Trials

Comparison of Carto Versus Ensite 3D Electroanatomical Mapping Systems for Arrhythmias Ablations

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

Three dimensional anatomical mapping is an established method facilitating ablation of cardiac arrhythmias. The most commonly used systems are CARTO® System (Biosense Webster, Inc., Diamond Bar, CA, USA) and EnSite NavX™ (St. Jude Medical, Inc., St. Paul, MN, USA). These two systems has been compared in only a few studies. Recent technical advances resulted in the development of new versions of both systems. To the best of the investigators knowledge no studies have been performed for direct comparison of the newer versions of these two systems. The aim of the study to compare two systems for the use in the ablation of complex arrhythmias.

NCT ID: NCT01069185 Completed - Cardiac Arrest Clinical Trials

Differences in Morbidity Between a Necessity Endotracheal Suctioning Protocol Versus a Routine Endotracheal Suctioning

Start date: February 2010
Phase: N/A
Study type: Interventional

Morbidity frequency associated to a endotracheal suctioning is different between a necessity endotracheal suctioning protocol versus a routine endotracheal protocol.