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Tachycardia, Ventricular clinical trials

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NCT ID: NCT01085435 Completed - Clinical trials for Tachycardia, Ventricular

Boston Scientific Post Market S-ICD Registry

EFFORTLESS
Start date: February 2, 2011
Phase:
Study type: Observational

The EFFORTLESS ICD Registry is an observational, standard of care evaluation designed to demonstrate the early, mid and long-term clinical effectiveness the Boston Scientific S-ICD System. In addition, analysis of resource utilization and costs will be performed to document treatment costs for periods defined by Registry endpoints. Protocol 90904928 restricts enrolment to patients over 18 years of age while protocol 90904925 allows all patients to be included.

NCT ID: NCT01064076 Active, not recruiting - Clinical trials for Tachycardia, Ventricular

S-ICD® System IDE Clinical Study

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

This clinical study is designed to evaluate the safety and effectiveness of the subcutaneous implantable defibrillator (S-ICD) System.

NCT ID: NCT01045668 Completed - Clinical trials for Ventricular Tachycardia

Ablation of Clinical Ventricular Tachycardia Versus Addition of Substrate Ablation on the Long Term Success Rate of VT Ablation

VISTA
Start date: January 2010
Phase: Phase 3
Study type: Interventional

This study aims to assess whether a combined technique of substrate ablation and ablation of the clinically presenting VT at the site of early activation is superior to ablation of the clinically presenting VT alone, in enhancing long-term success of VT ablation.

NCT ID: NCT01038960 Completed - Clinical trials for Ventricular Tachycardia

Exercise Training in ICD Recipients; Effect on Therapy Delivered, Depression and Anxiety

ETHIC
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Interventional study in patients with ICD. Controlled, open intervention with exercise training. Assessment of changes in physiological and psychological parameters.

NCT ID: NCT01032317 Completed - Atrial Fibrillation Clinical Trials

Study of a New Catheter Using Force Sensing Capabilities for the Treatment of Atrial Fibrillation and Ventricular Tachycardia

EZCF-125
Start date: November 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to study the treatment of Atrial Fibrillation and ischemic Ventricular Tachycardia using a RF ablation catheter with contact force sensing capabilities.

NCT ID: NCT01013714 Recruiting - Clinical trials for Ventricular Tachycardia

Cardiac Sympathetic Denervation for Prevention of Ventricular Tachyarrhythmias

PREVENT VT
Start date: July 26, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to examine the effect of cardiac sympathetic denervation (CSD) surgery on life threatening abnormal heart rhythms called ventricular tachycardia or ventricular fibrillation that can lead to sudden cardiac death. Subjects will be asked to participate in this research study if they have recurrent ventricular tachycardia (at least one ICD shock for ventricular tachycardia) and have undergone at least one catheter ablation procedure or have ventricular tachycardia or fibrillation that is not ablatable. The goal of this study is to determine whether cardiac sympathetic denervation can prevent these abnormal heart rhythms from occurring and therefore, prevent, ICD shocks which are not only painful, but have been shown to reduce quality of life and/or lead to depression, particularly in the period immediately after the shock.

NCT ID: NCT00989417 Completed - Clinical trials for Ventricular Fibrillation

Benefits of Implantable Cardioverter Defibrillator Follow-up Using Remote Monitoring

ECOST
Start date: January 2007
Phase: N/A
Study type: Interventional

In many aspects of every-day life, modern communication systems bring about a remarkable increase in comfort and safety by transmitting data and information in an easy and reliable manner. In order to provide these advantages also to patients with implantable cardioverter-defibrillators, as well as to their physicians, BIOTRONIK has developed a long-distance implant telemetry to enable periodic trend and event-triggered transmissions of implant data and intracardiac electrogram over distances of several meters. The data is received by a patient device and subsequently automatically transferred to a BIOTRONIK Service Center that provides it to the physician on a password secured internet site. Hence, the physician receives diagnostic information without the patient having to visit the physician (Home Monitoring, HM). New possibilities will arise for a detailed medical and event-correlated supervision of the patient's therapy using electrically active implants.

NCT ID: NCT00925522 Terminated - Clinical trials for Ischemic Ventricular Tachycardia

Therapy Cool Path Ablate VT

Ablate-VT
Start date: June 2009
Phase: N/A
Study type: Interventional

To demonstrate that ablation with the Therapy Cool Path Duo cardiac ablation system can eliminate ischemic VT and that its use does not result in an unacceptable risk of serious adverse events.

NCT ID: NCT00919373 Completed - Clinical trials for Coronary Artery Disease

Substrate Modification in Stable Ventricular Tachycardia in Addition to Implantable Cardioverter Defibrillator (ICD) Therapy

VTACH
Start date: July 2002
Phase: N/A
Study type: Interventional

The main objective of this study is to compare the time from randomization to the first recurrence of any ventricular tachycardia (VT) in patients undergoing VT ablation (for stable VTs) and substrate ablation (for unstable VTs) after an initial episode of stable VT and patients not undergoing ablation, with both groups under the protection of an ICD.

NCT ID: NCT00905853 Completed - Clinical trials for Recurrent Ventricular Tachycardia

Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy

VANISH
Start date: May 2009
Phase: Phase 4
Study type: Interventional

This study will compare aggressive antiarrhythmic therapy to catheter ablation for ventricular tachycardia in patients who have suffered prior myocardial infarction. The purpose of this study is to evaluate the optimal management of patients presenting with recurrent VT and receiving ICD therapy in spite of first-line antiarrhythmic drug therapy. The hypothesis is catheter ablation is superior to aggressive antiarrhythmic drug therapy for recurrent VT.