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Tachycardia, Ventricular clinical trials

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NCT ID: NCT02211456 Completed - Heart Failure Clinical Trials

An Assessment of Dual Site Left Ventricular Endocardial Pacing

DOUBLE-CRT
Start date: December 2014
Phase: N/A
Study type: Interventional

We are investigating ways to help patients with heart failure, which is caused by damaged hearts which function less well, and cause symptoms of breathlessness, fatigue, lack of energy and swelling. Cardiac Resynchronisation Therapy (CRT) pacemakers are used to improve the pumping function of the main heart chamber in certain suitable people with heart failure. CRT requires a pacemaker with 2 wires, one placed inside the right heart chamber and one normally placed on the outside of the left heart chamber. These two wires act together to re-time the coordination of the heartbeat, which is known to improve heart function. The investigators are assessing whether they might be able to improve heart function even more by placing two wires on the inside of the left heart chamber, rather than one around the outside. The investigators wish to assess whether: 1. Using two wires within the left side of the heart gives a greater increase in heart function than one. 2. It is possible to choose the best spot inside of the heart by measuring the pattern of the heart beat. 3. Is it possible to use a different type of heart monitor placed outside the body instead of a monitor wire inside the heart to assess improvement in heart function? They are investigating this in people with hearts that beat less effectively than normal.

NCT ID: NCT02130765 Terminated - Clinical trials for Monomorphic Ventricular Tachycardia

Substrate Targeted Ablation Using the FlexAbilityâ„¢ Ablation Catheter System for the Reduction of Ventricular Tachycardia

STAR-VT
Start date: November 2014
Phase: N/A
Study type: Interventional

To demonstrate that scar-based ventricular tachycardia (VT) ablation using the FlexAbilityâ„¢ ablation catheter system results in a superior clinical outcome compared to routine drug therapy in subjects with documented Monomorphic Ventricular Tachycardia [MMVT] (both ischemic and non-ischemic) while maintaining an acceptable safety profile.

NCT ID: NCT02114528 Terminated - Clinical trials for Ventricular Tachycardia

Anti-arrhythmic Therapy vs Catheter Ablation as First Line Treatment for AICD Shock Prevention

AVATAR
Start date: October 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether catheter based ablation is better than conventional anti-arrhythmic drug (AAD) therapy for reducing recurrent shocks in patients with an implantable cardioverter defibrillator (ICD). The second purpose of the study is to determine the safety of catheter-based ablation and the effect on quality of life of patients. The study hypothesis is that catheter ablation is superior to AAD therapy in preventing recurrent ventricular arrhythmia in such subjects. This is a pilot trial which will provide data regarding recruitment potential and the feasibility of conducting a larger trial.

NCT ID: NCT02083016 Completed - Clinical trials for Ventricular Tachycardia

Ultra-high Density Mapping With Multielectrode Catheter vs Conventional Point by Point Mapping for Ventricular Tachycardia Substrate Ablation

Start date: April 2014
Phase: Phase 4
Study type: Interventional

Ultra-high density mapping with multielectrode catheter may improve slow conduction channels identification in ventricular tachycardia substrate ablation procedures compared to conventional point by point mapping. This study compares the ability of both mapping catheters to detect slow conduction channels in areas of myocardial scar and their utility to assess substrate modification after ablation.

NCT ID: NCT02072707 Completed - Clinical trials for Tachycardia, Ventricular

Efficacy and Safety of Epicardial VT Ablation Using Contact Force Irrigated Tip Catheter - Pilot Study

Start date: April 2014
Phase: N/A
Study type: Interventional

The investigators hypothesized that combined endocardial and epicardial VT ablation using contact sensor irrigated catheter is safe and achieves a lower recurrence rate than endocardial only ablation in ischemic and non-ischemic patients, for this the investigators will randomize 20 patients in two groups, one with endocardial only ablation and other with combined endocardial and epicardial ablation.

NCT ID: NCT02071511 Terminated - Clinical trials for Ventricular Tachycardia

Renal Denervation In Patient Undergoing VT Ablation:Combined Renal Denervation and VT Ablation vs. Simply VT Ablation

ARDEVAT
Start date: January 2014
Phase: N/A
Study type: Interventional

Study hypothesis: With optimal medical therapy and repeated ablations, an additional renal denervation may have protective effects in terms of vegetative intrinsic activity and lead to a significant reduction in VT Burdens. Study design: Multicenter, randomized, prospective, single-blind clinical trial.

NCT ID: NCT02014675 Active, not recruiting - Heart Failure Clinical Trials

SD01 Registry (SD01 ICD Lead)

SD01 Registry
Start date: March 2014
Phase:
Study type: Observational [Patient Registry]

This registry is designed to gather further evidence, in addition to the SD01 Master Study, for the safety and efficacy of the SD01 ICD lead.

NCT ID: NCT02008461 Recruiting - Clinical trials for Supra-ventricular Tachyarrhythmias

Botulinum Toxin Injection for Preventing Secondary Atrial Fibrillation in Patient With Supra-ventricular Tachyarrythmias

Start date: June 2013
Phase: Phase 2
Study type: Interventional

The investigators have conducted a prospective, double-blind, randomized study to assess the comparative safety and efficacy of two different ablation strategies, RFA versus RFA plus botulinum toxin injection, in patients with supra-ventricular tachyarrhythmias. Results were assessed with the use of an implanted monitoring device (IMD).

NCT ID: NCT02003001 Recruiting - Clinical trials for Ventricular Tachycardia

Botulinum Toxin Injection to Prevent Ventricular Arrhythmias

Start date: June 2013
Phase: Phase 1
Study type: Interventional

The aim of this prospective non-randomized study was to assess the efficacy and safety of endomyocardial botulinum toxin injection in left ventricle for preventing ventricular arrhythmias.

NCT ID: NCT01989299 Completed - Clinical trials for Heart Failure With Preserved Ejection Fraction (HFpEF)

Ventricular Tachyarrhythmia Detection by Implantable Loop Recording in Patients With Heart Failure and Preserved Ejection Fraction

VIP-HF
Start date: November 2014
Phase:
Study type: Observational [Patient Registry]

Heart failure with preserved ejection fraction (HFPEF) is a large medical problem, for which no drug or device has a recommendation in current heart failure guidelines. Sudden cardiac death is suggested as the most common cause of death in HFPEF patients, although data is sparse. Use of an Implantable Loop Recorder (ILR) may be useful in patients with HFPEF to evaluate the incidence of sustained ventricular tachyarrhythmias. If ventricular tachyarrhythmias are seem frequently, treatment with an Implantable Cardioverter Defibrillator (ICD) may be an option in the future.