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Tachycardia clinical trials

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NCT ID: NCT00606567 Completed - Clinical trials for Ventricular Fibrillation

A Randomized Trial of Remote Monitoring of Implantable Cardioverter Defibrillators Versus Quarterly Device Interrogations in Clinic

Medusa SAK
Start date: December 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if remote monitoring of implantable cardioverter defibrillators (ICD), compared with quarterly device interrogations in clinic, will improve patients' outcomes and satisfaction and will reduce health care costs.

NCT ID: NCT00585871 Withdrawn - Clinical trials for Ventricular Tachycardia

Clonidine to Prevent Implantable Cardiovertor Defibrillator Firing

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

Cardiac arrest or sustained VT (ventricular tachycardia) in patients with heart disease is best treated with an ICD (implantable cardioverter defibrillator). However, the ICD alone is not appropriate therapy for patients with frequent VT episodes. In fact frequent shocks for VT may predict a poorer prognosis. Anti-arrhythmic drugs are co-administered with ICDs in up to 50% of patients to prevent VT episodes, but antiarrhythmic drugs may have harmful effects. Thus improved drugs to prevent VT without interfering with ICD function are needed. Recent data including our own suggest that clonidine may be a new therapy to prevent ICD shocks. It may act centrally on sympathetic outflow and peripherally and selectively on cardiac Purkinje, to suppress and control VT occurring in patients. Our purpose is to test the hypothesis that clonidine reduces frequent VT better than beta blocker in patients with ICDs. After informed consent patients will be randomized in a single blind fashion to either clonidine or metoprolol given three times per day. Other prescribed drugs may be adjusted to promote toleration of the study drug. ICD interrogations of episodes of VT will be the primary endpoint. Device based NIPS (non-invasive programmed stimulation) testing in a subset of these patients will allow mechanistic understanding of the clonidine effect. All of the procedural techniques are in place as performed clinically; preliminary data are given showing feasibility of the project.

NCT ID: NCT00584649 Terminated - Clinical trials for Inappropriate Sinus Tachycardia

Ablation of Inappropriate Sinus Tachycardia

IST
Start date: April 2004
Phase: N/A
Study type: Interventional

Hypothesis- Radiofrequency ablation, targeting the sympathetic input of the sinus node identified by 20Hz stimulation at the junction of the superior vena cava and the right atrium, will effectively reduce sinus rate acutely and will reduce palpitations due to inappropriate sinus tachycardia without the need for pacemaker implantation due to sinus node dysfunction post ablation.

NCT ID: NCT00583297 Completed - Clinical trials for Cardiovascular Diseases

Genetic Substudy of the Alternans Before Cardioverter Defibrillator (ABCD) Trial

ABCD
Start date: January 2007
Phase: N/A
Study type: Observational

The ABCD clinical study (ClinicalTrials.gov Identifier NCT00187291) was designed to determine if a T-Wave Alternans (TWA) test is equivalent to an Electrophysiology Study (EPS) in predicting life-threatening heart rhythms in patients with ischemic heart disease, left ventricular dysfunction, and non-sustained tachycardia. The purpose of the ABCD Genetic sub-study is to identify genetic markers that predict TWA status and arrhythmia risk in this same population.

NCT ID: NCT00583284 Terminated - Clinical trials for Ventricular Tachycardia

The Use of CT to Identify Damaged Heart Muscle in Patients Undergoing Ventricular Tachycardia Ablation.

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

Patients with ventricular tachycardia (VT) undergo catheter ablation. During the ablation procedure, the heart is mapped to determine areas of heart muscle damage. The heart scarring areas are often the source of the VT. Delayed enhancement CT has recently been used to determine areas of scarring . This study is to determine if the areas of damaged heart muscle mapped with the delayed enhancement CT correlate with the same areas that are determined during the catheter ablation.

NCT ID: NCT00581633 Active, not recruiting - Clinical trials for Postural Tachycardia Syndrome

Acute Salt Handling in Orthostatic Intolerance

Start date: February 2007
Phase: N/A
Study type: Interventional

The investigators will test the hypothesis that patients with chronic orthostatic intolerance or postural orthostatic tachycardia syndrome (OI or POTS) will be unable to conserve urinary sodium as compared to healthy control subjects.

NCT ID: NCT00581022 Completed - Clinical trials for Postural Tachycardia Syndrome

Objective Sleep Disturbances in Orthostatic Intolerance

Start date: November 2006
Phase:
Study type: Observational

We wish to study sleep architecture in patients with chronic orthostatic intolerance. We will test the null hypothesis that there is no difference in time during the various phases of sleep between patients and healthy control subjects.

NCT ID: NCT00580619 Completed - Clinical trials for Chronic Fatigue Syndrome

Autonomic Nervous System and Chronic Fatigue Syndrome

CFS&ANS
Start date: April 2007
Phase: Phase 1
Study type: Interventional

The investigators propose to test the hypothesis that the sympathetic nervous system contributes to the cardiovascular and inflammatory abnormalities present in the chronic fatigue syndrome (CFS) and, in particular in the subset of patients characterized by postural tachycardia syndrome (POTS). CFS and POTS are seen mostly in otherwise normal young women, and are the cause of significant disability. A substantial proportion of patients referred for evaluation of POTS met diagnostic criteria for CFS and, conversely, a subset of patients referred for treatment for CFS have POTS. The investigators hypothesize that sympathetic activation underlies the pathophysiology of patients in whom CFS and POTS overlap (CFS-P).

NCT ID: NCT00559559 Completed - Clinical trials for Tachycardia, Ventricular

PAtient NOtifier Feature for Reduction of Anxiety

Panoramic
Start date: December 2007
Phase: N/A
Study type: Interventional

This study is intended to look at the effect of the SJM vibrating Patient Notifierâ„¢ system, which will warn the patient of possible failures of the implanted system, on reducing patient device related anxiety

NCT ID: NCT00558857 Terminated - Clinical trials for Ischemic Ventricular Tachycardia

Dynamic Substrate Mapping (DSM) for Ischemic VT

DSM
Start date: July 2007
Phase: Phase 1
Study type: Interventional

This is a prospective, non-randomized study to determine the feasibility of using a new technique called Dynamic Substrate Mapping (DSM) to help guide the treatment of ischemic ventricular tachycardia (IVT). We hypothesize that DSM will lead to simpler, more effective ablation of IVT. Results from this study will be used to determine if further clinical investigation is warranted.