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Arrhythmia clinical trials

View clinical trials related to Arrhythmia.

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NCT ID: NCT02045992 Recruiting - Arrhythmia Clinical Trials

Arrhythmic Effects of Hight Dose Caffeine

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

Heart failure patients represent a group of individuals at higher risk for cardiac arrhythmias. There is a perception that caffeine consumption may represent an increase in this risk. Although the medical staff and health professionals suggest a reduction in the intake of this substance to patients considered at risk, there is no scientific proof for this recommendation. Some animal studies suggest a possible association between arrhythmias and caffeine use with higher doses, but this finding did not appear in human studies. In particular, little is known about the association between caffeine consumption and arrhythmias in patients with heart failure, especially at higher doses of consumption. More specific and safe guidelines on caffeine consumption are needed.

NCT ID: NCT01991223 Recruiting - Pain Clinical Trials

Dexmedetomidine for Catheter-related Bladder Discomfort

CRBDEX
Start date: November 2013
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy of dexmedetomidine for the prevention of catheter-related bladder discomfort

NCT ID: NCT01906827 Recruiting - Arrhythmia Clinical Trials

P-wave Duration and Dispersion in Intrahepatic Cholestasis of Pregnancy

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

The bile acids has been demonstrated to cause arrhythmia and abnormal calcium dynamics in cultured neonatal rat cardiomyocytes. Bile acids may alter maternal cardiomyocyte function like fetus.Increased P-wave duration and P-wave dispersion have been reported in various clinical settings. The investigators hypothesized that PWD and p wave duration may affect in pregnancy with ICP.

NCT ID: NCT01265771 Recruiting - Children Clinical Trials

Optimizing Diagnostics Of Arrhythmia Events In Children Using Intelligent Telemetric Solutions

TELEMARC2
Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess efficacy of prolonged Full Disclosure electrocardiogram (ECG) monitoring and signal analysis using advanced telemetric technology to diagnose arrhythmia in comparison with standard diagnostic procedure.

NCT ID: NCT01265758 Recruiting - Atrial Fibrillation Clinical Trials

Telemetric Arrhythmia Diagnosis in Adults

TELEMARC1
Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess efficacy of prolonged Full Disclosure electrocardiogram (ECG) monitoring and signal analysis using advanced telemetric technology in comparison with a standard Holter ECG recording and an Event Holter recording to diagnose cardiac arrhythmia.

NCT ID: NCT00754663 Recruiting - Arrhythmia Clinical Trials

Exercise Training in Patients With Cardioverter-Defibrillators

BETA
Start date: May 2008
Phase: N/A
Study type: Interventional

Exercise therapy has proven to be an effective additive therapy in patients with cardiovascular diseases. The prognostic value of physical activity is well established in patients with congestive heart failure. Therefore the investigators assumed that the population of patients with implantable cardioverter-defibrillators (ICD) with impaired left ventricular function may also benefit from a cardiovascular training in terms of improved quality of life and reduction of ventricular arrhythmia. The data on feasibility, risk and therapeutic effects of exercise training are very limited or not available. This prospective randomized study examines the feasibility and benefits of exercise therapy in patients with ICD and congestive heart failure.

NCT ID: NCT00733590 Recruiting - Clinical trials for Heart Failure, Congestive

Prospective Observational Study of the ICD in Sudden Cardiac Death Prevention

PROSe-ICD
Start date: June 2003
Phase:
Study type: Observational

The overall hypothesis of this study is that subtle interactions between structural (substrate) and functional (trigger) abnormalities of the heart, some of which are genetically-determined, can be used to identify patients at high risk of sudden cardiac death (SCD). Such information may be used to better define patients most likely to benefit from replacement of an internal defibrillator (ICD). The prospective, observational study to enroll, categorize and follow patients who receive an ICD pulse generator replacement for primary prevention of SCD (PROSe-ICD) was established to : 1. to gain a better understanding of the biological mechanisms that predispose to SCD 2. to develop readily determined clinical, electrocardiographic, genetic and blood protein markers identify patients with an increased risk of dying suddenly

NCT ID: NCT00483873 Recruiting - Cardiac Arrest Clinical Trials

Cardiac Arrest Recovery EEG Study

CARES
Start date: August 2007
Phase: N/A
Study type: Observational

The purpose of the study is to collect EEG's as close to the cardiac arrest as possible using a standard hospital EEG machine and an investigational EEG device to help determine the neurological status of the cardiac arrest patient and to help decide on possible treatment and chance of recovery. The investigational EEG machine will be simple to operate as well as easy to interpret for the clinician and the nurses. It is not to replace the electrophysiologist interpretation but to determine ealy on if further evaluation and treatment can help the patient.

NCT ID: NCT00282620 Recruiting - Quality of Life Clinical Trials

Magnesium to Reduce Implantable Cardioverter Defibrillator (ICD) Shocks and Improve Patient's Quality of Life.

Start date: January 2006
Phase: Phase 4
Study type: Interventional

This study is being conducted to see if magnesium can reduce the number of shocks patients with ICDs experience and to see if magnesium supplementation improves patients quality of life.

NCT ID: NCT00271180 Recruiting - Heart Failure Clinical Trials

Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products

PPR
Start date: January 1983
Phase:
Study type: Observational

The main purpose of the Product Performance Report (formerly referred to as System Longevity Study) is to evaluate long-term performance of Medtronic market-released cardiac rhythm products by analyzing product survival probabilities.