Clinical Trials Directory

Trials / Terminated

TerminatedNCT01401608

Stereotaxis Idiopathic Ventricular Tachycardia (VT) Study

RF Ablation of Idiopathic VT and PVCs Using Remote Magnetic Navigation

Status
Terminated
Phase
Study type
Observational
Enrollment
6 (actual)
Sponsor
Stereotaxis · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This study will assess the outcomes of using magnetic navigation to treat ventricular tachycardia (VT) or premature ventricular contractions (PVCs) that occur for unknown reasons and are not related to structural heart disease.

Detailed description

During conventional ventricular arrhythmia ablation procedures, simply contacting the cardiac wall can significantly alter the electrocardiogram. Induction of ventricular ectopy is important in determining the focus of the arrhythmogenic tissue during an electrophysiology (EP) procedure; however, instrumentation with stiff ablation catheters can temporarily eliminate VT during the mapping portion of the procedure making it difficult to track the arrhythmia prior to ablating the tissue responsible for its genesis. The catheters used with the Stereotaxis Magnetic Navigation System (MNS) are less stiff compared to manual catheters since no pull wires are required to deflect the distal tip. Large external magnets positioned on either side of the EP procedure table create a magnetic field within the patient's chest. These large magnets (in direct relationship to the magnetic field) can be manipulated using specialized software. The physician controls the distal tip of the catheter by using the software while remotely using a catheter advancing system (QuickCAS®, Stereotaxis, Inc, St. Louis, MO) to reach the desired location within the heart. The soft catheters may provide a unique quality to the electrophysiologist who may assist by providing accurate maps without temporarily eliminating the ventricular ectopy due to excessive mechanical forces applied to the cardiac tissue. This study will assess the physician's ability to appropriately map and ablate the ventricular substrate using remote magnetic technology. All devices are approved by FDA and no off-label use of the products is mandated within the protocol.

Conditions

Interventions

TypeNameDescription
DEVICERF AblationAblation of arrhythmogenic ventricular tissue

Timeline

Start date
2011-03-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2011-07-25
Last updated
2015-05-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01401608. Inclusion in this directory is not an endorsement.