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Arrhythmias clinical trials

View clinical trials related to Arrhythmias.

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NCT ID: NCT00919646 Completed - Arrhythmias Clinical Trials

Monitoring Arrhythmia Patients in in Hospital Monitoring

ADAM
Start date: April 2009
Phase: N/A
Study type: Observational

This is a prospective, single center, non-randomized study to evaluate the arrhythmia monitoring performance of the AVIVO™ System in a hospital setting.

NCT ID: NCT00919568 Completed - Arrhythmias Clinical Trials

Monitoring Arrhythmia Patients (IMPACT)

Start date: June 2009
Phase: N/A
Study type: Observational

Prospective, multicenter, non-randomized study to determine the performance of NUVANT Mobile Cardiac Telemetry system in arrhythmia detection.

NCT ID: NCT00919087 Completed - Arrhythmias Clinical Trials

Non Invasive Arrhythmia Detection in Hospital Settings

EVE
Start date: April 2009
Phase: N/A
Study type: Observational

This is a prospective, single center, non-randomized study to evaluate the arrhythmia detection performance during ventricular events.

NCT ID: NCT00751738 Completed - Arrhythmias Clinical Trials

Long Term Safety of 125 mg Per Day of Oral Azimilide in Patients With Implantable Cardioverter Defibrillator (ICDs)

Start date: October 2002
Phase: Phase 3
Study type: Interventional

This is an open-label, multi-center, long-term, (open-ended) safety study with 125 mg per day of azimilide in patients who completed protocol 2000098.

NCT ID: NCT00669838 Completed - Anxiety Clinical Trials

Anesthesia for Dental Treatment in Cardiac Patients: Lidocaine Comparative Study

Start date: January 2003
Phase: N/A
Study type: Observational

Prospective, randomized double-blinded study to investigate hemodynamic changes in valvular cardiac patients during dental treatment with the use of a local anesthesia containing epinephrine.

NCT ID: NCT00669682 Completed - Clinical trials for Congestive Heart Failure

T-wave Alternans and Intrathoracic Impedance Measurements

Start date: August 2008
Phase: N/A
Study type: Observational

T-wave alternans is a test that is currently being used to risk stratify patients with structural heart disease for sudden cardiac death. The mechanism of T-wave alternans is unclear, but may share a common abnormality with conditions of cardiac fluid overload such as heart failure, which is altered intracellular calcium handling. Current Medtronic implantable defibrillators have the capability of monitoring cardiac fluid status via transthoracic impedance measurements. The purpose of this study is to determine if a correlation exists between T-wave alternans status and cardiac volume status, as determined by transthoracic impedance measurements. Secondarily, the study seeks to examine the relationship between arrhythmia frequency and T-wave alternans or cardiac volume status.

NCT ID: NCT00589849 Completed - Clinical trials for Myocardial Infarction

T-Wave Alternans in Acute Myocardial Infarction: An Evaluation of the Time of Testing on Its Prognostic Accuracy

Start date: May 2006
Phase: N/A
Study type: Observational

T-wave alternans is an electrocardiographic finding that has been shown to predict the occurrence of future cardiac arrhythmias in patients who have had a heart attack. What is unknown about T-wave alternans testing is when is the best time to perform the test. In most studies, T-wave alternans testing is conducted 4 weeks or more after a heart attack. It is unknown if T-wave alternans testing performed prior to hospital discharge in heart attack patients is reliable. The objective of this project is to determine the diagnostic accuracy of T-wave alternans testing performed prior to hospital discharge and again at 30 days after hospital discharge in patients who have suffered a heart attack.

NCT ID: NCT00284453 Completed - Arrhythmias Clinical Trials

Ventricular Tachyarrhythmia (VT) Storm, Gene Expression in Implantable Cardioverter Defibrillator (ICD) Patients With Electrical Storm

Start date: August 26, 2008
Phase:
Study type: Observational

The purpose of the proposed pilot study is to identify factors which are associated with periods of high ventricular arrhythmia burden. This will be performed by analysis of gene expression from peripheral blood samples.