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Tachycardia clinical trials

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NCT ID: NCT01576042 Terminated - Clinical trials for Ventricular Tachycardia

Pilot Study of Catheter Ablation for Ventricular Tachycardia in Patients With an Implantable Cardioverter Defibrillator

CALYPSO
Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this pilot trial is to determine the feasibility of a large, multi-center randomized clinical trial aimed to test whether a treatment strategy of percutaneous catheter ablation of ventricular tachycardia (VT) is superior to state-of-the-art pharmacologic therapy at reducing all-cause mortality in patients with an implantable cardioverter defibrillator (ICD) who receive therapy for VT in the absence of any reversible cause.

NCT ID: NCT01572246 Completed - Heart Failure Clinical Trials

Effects of Monopolar Electrocautery Use During Surgery on Implanted Cardiac Defibrillators

Start date: May 2012
Phase: N/A
Study type: Observational

This observational protocol will evaluate the effects of monopolar electrocautery (ME) on implantable cardioverter defibrillators (ICDs) in patients undergoing surgery. ME can cause electromagnetic interference (EMI) leading to ICD damage or inadvertent ICD discharge (shocks). Recommended practice calls for the preoperative reprogramming of ICDs when ME will be used to prevent patients from receiving inadvertent shocks. This requires the presence of someone trained in ICD programming, but a trained person is not always readily available. In this study the investigators will reprogram ICDs prior to surgery according to current practice, but will also record what would have happened had the ICD reprogramming not occurred ("detection on" but "therapy off"). In addition, the investigators will evaluate the effect of the location of the electrosurgery unit (ESU) return pad on the incidence of EMI. The investigators hypothesize that directing the current return path away from the ICD will result in lower EMI rates than previously described.

NCT ID: NCT01563107 Completed - Clinical trials for Postural Orthostatic Tachycardia Syndrome

Dietary Sodium's Effect on Urinary Sodium and Dopamine Excretion in Patients With Postural Tachycardia Syndrome

Start date: March 2012
Phase: N/A
Study type: Interventional

Patients with Postural Tachycardia Syndrome (POTS) may not adequately expand their plasma volume in response to a high sodium diet. Mechanisms involved in the regulation of plasma volume, such as the renin-angiotensin-aldosterone system and renal dopamine (DA), may be impaired in POTS and may respond inappropriately to changes in dietary sodium. The investigators propose that the changes in urinary sodium and dopamine excretion caused by consuming low-sodium and high-sodium diets will be different between patients with POTS and healthy volunteers. The purpose of this study is to determine (1) whether changes in dietary sodium level appropriately influence sodium excretion in POTS; (2) whether changes in dietary sodium level appropriately influence DA excretion in POTS; (3) whether a high dietary sodium level appropriately expands plasma volume in POTS; and (4) whether patients with POTS have improvements in their orthostatic tachycardia and symptoms as a result of a high dietary sodium level.

NCT ID: NCT01558830 Unknown status - Clinical trials for Coronary Artery Disease

Safety of Amiodarone and Ranolazine Together in Patients With Angina

SARA
Start date: January 2012
Phase: Phase 4
Study type: Interventional

Ranolazine is an effective and remarkably safe agent for the treatment of patients with chronic stable angina, but its inhibition of voltage gated potassium channels and electrocardiogram (EKG) corrected QT (QTc) prolongation properties have lead many to question its safety when combined with antiarrhythmic drugs. The investigators have proposed a study to determine the safety of ranolazine in patients with chronic stable angina who also take amiodarone. And are conducting a prospective single-center randomized single-blinded placebo controlled trial to run out of our large cardiology practice setting at Cardiovascular Consultants of Nevada. The hypothesis is that there will be no difference in the ventricular arrhythmia burden. The primary outcome will be the measurement of ventricular arrhythmia episodes on serial holter monitor and other serially acquired recordings (such as electrocardiogram, pacemaker or implantable defibrillator (ICD) data, and stress test data) over a three month trial period.

NCT ID: NCT01557842 Terminated - Clinical trials for Ventricular Tachycardia

Early Ablation Therapy for the Treatment of Ischemic Ventricular Tachycardia in Patients With Implantable Cardioverter Defibrillators

ASPIRE
Start date: June 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if early ablation (i.e., ablation of ventricular tachycardia in patients with infrequent VT episodes) is more effective than medical therapy alone for the treatment of ischemic ventricular tachycardia in patients with Implantable Cardioverter Defibrillators (ICDs) who continue to have episodes of ventricular tachycardia despite drug therapy.

NCT ID: NCT01550315 Completed - Clinical trials for Postural Tachycardia Syndrome (POTS)

Effect of Dietary Sodium Intake on Vascular Endothelium

Start date: April 2012
Phase: N/A
Study type: Interventional

The investigators will test the hypothesis that markers of vascular endothelial dysfunction will be exaggerated acutely with an extreme high sodium diet compared to an extreme low-sodium diet. The investigators will compare patients with postural orthostatic tachycardia (POTS) to healthy control subjects.

NCT ID: NCT01548755 Not yet recruiting - Tachycardia Clinical Trials

The Western Galilee Hospital in Nahariya Home Monitoring Registry

Start date: April 2012
Phase: N/A
Study type: Observational

The purpose of this study is to study workload assessment of home monitoring based follow up for ICD or CRTD implanted patient.

NCT ID: NCT01547208 Recruiting - Clinical trials for Ventricular Tachycardias

Does Timing of VT Ablation Affect Prognosis in Patients With an Implantable Cardioverter-defibrillator?

PARTITA
Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the burden of untreated non-sustained ventricular tachycardias (VTs), or episodes treated with anti-tachycardia pacing, correlates with appropriate implantable cardiac defibrillator (ICD) shock therapies and to evaluate if the timing of radiofrequency VT ablation affects the prognosis of ICD recipients.

NCT ID: NCT01547117 Completed - Clinical trials for Postural Orthostatic Tachycardia Syndrome

Dietary Salt in Postural Tachycardia Syndrome

Start date: March 2012
Phase: N/A
Study type: Interventional

Patients with POTS may not adequately expand their plasma volume in response to a high-sodium (Na+) diet. Mechanisms involved in the regulation of plasma volume, such as the renin-angiotensin-aldosterone system and renal dopamine, may be impaired in POTS and may respond inappropriately to changes in dietary sodium.The purpose of this study is to determine (1) whether a high dietary sodium level appropriately expands plasma volume in POTS; (2) whether plasma renin activity and aldosterone are modified appropriately by changes in dietary sodium in POTS; and (3) whether patients with POTS have improvements in their orthostatic tachycardia and symptoms as a result of a high dietary sodium level.

NCT ID: NCT01546207 Terminated - Clinical trials for Ventricular Tachycardia

Stepwise Approach To sUbstrate Modification for Ventricular Tachycardia

STRATUM VT
Start date: September 2011
Phase: N/A
Study type: Interventional

The goal of this trial is to test the impact of a step-wise approach for catheter ablation of recurrent ventricular tachycardia, (irregular heart rhythms that originate in the bottom chambers of the heart), in patients with a previous heart attack for whom catheter ablation is clinically indicated.