Clinical Evaluation of Therapy Cool Path Duo Cardiac Ablation System for the Treatment of Ischemic Ventricular Tachycardia (VT) (Ablate-VT)

This study has been completed.
Sponsor:
Information provided by:
St. Jude Medical
ClinicalTrials.gov Identifier:
NCT00925522
First received: June 8, 2009
Last updated: July 22, 2011
Last verified: July 2011

June 8, 2009
July 22, 2011
June 2009
April 2010   (final data collection date for primary outcome measure)
  • Primary Safety is defined as the incidence of intra-procedural, acute or sub-chronic, serious cardiac adverse events, up to 7 days post-procedure. [ Time Frame: 7 days ] [ Designated as safety issue: Yes ]
  • Acute Success is achieved when all clinically relevant VT substrates (spontaneous and induced VT episodes) are terminated and no longer inducible upon hospital discharge (i.e., last study ablation procedure prior to hospital discharge). [ Time Frame: Hospital Discharge ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00925522 on ClinicalTrials.gov Archive Site
Chronic Success is defined at 6 months following the RF ablation procedure as no recurrence of clinically relevant VT(s) that were targeted at ablation. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Chronic Success is defined as no recurrence of VT episodes at 6 months post ablation. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Clinical Evaluation of Therapy Cool Path Duo Cardiac Ablation System for the Treatment of Ischemic Ventricular Tachycardia (VT)
Clinical Evaluation of Therapy Cool Path Duo Cardiac Ablation System for the Treatment of Ischemic Ventricular Tachycardia (VT)

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.

Ventricular Tachycardia (VT) is a common complication of ischemic heart disease that is often life threatening. Ventricular tachycardia is defined as three or more beats of ventricular origin in succession at a rate greater than 100 beats per minute. There are no normal QRS complexes associated with VT, and the rhythm is usually regular. Patients with VT experience unpleasant heart palpitations, dyspnea, and syncope, all of which decrease their overall quality of life. They also suffer the consequences of impaired hemodynamics, loss of cardiac efficiency, and are at an increased risk of sudden cardiac death (SCD), which accounts for approximately half of all deaths from patients with cardiovascular disease.

Historically, antiarrhythmic medications served as the first line therapy for the treatment of VT, in spite of low efficacy and high recurrence rates. But in recent years, internal cardioverter defibrillators (ICDs) have become the treatment of choice. Although, ICDs are effective in terminating most arrhythmias, rarely does so without some episodes requiring poorly tolerated shock therapy. Ablative therapy offers an important option for frequent control with the potential for long-term VT elimination. Radiofrequency catheter ablation offers the ability to provide immediate control of recurrent VT. Since the early 2000's, strategies, tools, and techniques have been improving to identify key ablation sites and to deliver effective lesions.

Radiofrequency ablation is successful in treating some but not all arrhythmias. With non irrigated technology it has been difficult to ablate ischemic VT. This may be due to an inadequate lesion size. Irrigated electrodes were developed to create larger lesions. Open irrigation at the catheter tip not only produces larger lesions, but also helps reduce the risk of coagulum (clots) and charring due to high temperatures.

Interventional
Phase 2
Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Ischemic Ventricular Tachycardia
Device: Therapy Cool Path Duo Cardiac Ablation System

Consists of the following three system components:

A flexible, insulated 7F all braided catheter that contains an internal lumen connected to 12 open conduits at the 4mm tip electrode for infusion of heparinized saline during radiofrequency ablation; records intracardiac electrograms and can be utilized for cardiac simulation during diagnostic electrophysiologic studies/evaluation.

The 1500T9-VT generator is a microprocessor-controlled device that produces a continuous unmodulated radiofrequency (RF) output of 485 kHz. The Generator will be used in Temperature Control mode only. The catheter delivers the RF power from the generator in a monopolar mode between its distal electrode (tip electrode) and a large indifferent electrode.

The Cool Point ™ Irrigation Pump and Cool Point™ Tubing Set is an external volumetric pump that is intended for use in administration of general I.V. fluids to patient's vascular system through the catheter in the hospital environment.

Experimental: Therapy Cool Path Duo Cardiac Ablation System
Intervention: Device: Therapy Cool Path Duo Cardiac Ablation System
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
July 2011
April 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patient is 18 years of age or older
  • Patient has an ICD or will be implanted with one prior to discharge of ablation procedure
  • Patient has had at least 2 documented spontaneous episode of sustained ischemic VT within the previous 6 months
  • Patient is resistant, intolerant or refractory to at least one Class I or III AAD
  • Patient has been informed of the nature of the study and has agreed to its provisions and provided written informed consent approved by the Institutional Review Board

Exclusion Criteria:

  • Non-ischemic VT
  • History of stroke or transient ischemic attack within 6 months prior to enrollment
  • MI or previous cardiac surgery within 2 months prior to enrollment
  • Patient is pregnant or nursing
  • Patient has chronic NYHA class IV heart failure
  • Limited life expectancy of 6 months or less
  • Patient is currently participating in another investigational drug or device study
  • Patient is unable or unwilling to cooperate with the study procedures
  • Known presence of intracardiac thrombi
  • Severe aortic stenosis or flailed mitral valve
  • Major contraindication to anticoagulation therapy or coagulation disorder
  • Left Ventricular Ejection Fraction <10%
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00925522
G080076
No
St Jude Medical, St. Jude Medical
St. Jude Medical
Not Provided
Principal Investigator: G. Neal Kay, M.D. University of Alabama at Birmingham
St. Jude Medical
July 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP