Arrhythmias Clinical Trial
Official title:
Comparative Study of Two 3D Electroanatomical Mapping Systems for Ablations of Different Complex Arrhythmias
Verified date | April 2017 |
Source | Rabin Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Three dimensional anatomical mapping is an established method facilitating ablation of cardiac arrhythmias. The most commonly used systems are CARTO® System (Biosense Webster, Inc., Diamond Bar, CA, USA) and EnSite NavX™ (St. Jude Medical, Inc., St. Paul, MN, USA). These two systems has been compared in only a few studies. Recent technical advances resulted in the development of new versions of both systems. To the best of the investigators knowledge no studies have been performed for direct comparison of the newer versions of these two systems. The aim of the study to compare two systems for the use in the ablation of complex arrhythmias.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | October 2016 |
Est. primary completion date | July 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. Age 18- 80. 2. Ability to sign informed consent. 3. History of one of the following arrhythmias requiring the use of 3D electroanatomical mapping: - Symptomatic paroxysmal or persistent atrial fibrillation with failed treatment of at least two anti-arrhythmic drugs. - Ischemic ventricular tachycardia necessitating ablation as per decision of electrophysiologist. - Symptomatic atrial tachycardia after failed medical treatment. - Symptomatic idiopathic ventricular tachycardia. Exclusion Criteria: 1. Unstable patients not allowing performing procedure more than 2 hours 2. Patients planned for one of the two systems compared for whatever reason Ex. procedure planned with NAVX system Array Balloon). |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Rabin Medical Center |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Procedure duration | Average procedure duration (needle to catheters withdrawal) | Procedure duration - average expected 2.5 hours | |
Secondary | Fluoroscopy time | Average fluro time in each of groups. | Procedures will be evaluated for the fluoro time, expected average 30 min | |
Secondary | Procedure success | Recurrency of the arrhythmia assessed by blinded electrophysiologist | Patients will be followed for one year for recurrency of arrhythmia |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03289429 -
Antiarrhythmic and Cardioprotective Effects of Atorvastatin Versus Magnesium Sulfate in Cardiac Valve Replacement Surgery
|
Phase 4 | |
Unknown status |
NCT01834872 -
Safety and Feasibility of Arrhythmia Ablation Using the Amigo Remote Robotic System as Compared With Manual Ablation
|
Phase 4 | |
Withdrawn |
NCT01026961 -
Safety of Phenylephrine Hydrochloride, Acetaminophen, Dimethindene Maleate Compared to Phenylephrine Hydrochloride Alone in Healthy Volunteers
|
Phase 1/Phase 2 | |
Not yet recruiting |
NCT05994755 -
Association Between Cardiac ARRHYTHMIAs and Glycemic Variability in Patient With Type 2 Diabetes Monitored Through FREEstyle Libre and Bluetooth Technology.
|
||
Not yet recruiting |
NCT06039176 -
Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future
|
||
Withdrawn |
NCT02575534 -
Acute Mechanical Response to Anti-arrhythmic Drug Therapy
|
N/A | |
Completed |
NCT02598258 -
Hemodynamic Effects of Dry Sauna Followed by Cold Water Immersion in Healthy Subjects
|
N/A | |
Withdrawn |
NCT00580255 -
Comparison Study of BNP and Thoracic Impedance Measurements on Arrhythmias
|
N/A | |
Completed |
NCT00751738 -
Long Term Safety of 125 mg Per Day of Oral Azimilide in Patients With Implantable Cardioverter Defibrillator (ICDs)
|
Phase 3 | |
Completed |
NCT02629445 -
HIPACE High Frequency Low Energy Pacing to Terminate Fast Ventricular Arrythmias
|
N/A | |
Recruiting |
NCT04563091 -
Potassium Kinetic During and After Hemodialysis and Potassium Profiling to Prevent Arrhythmias
|
N/A | |
Completed |
NCT00589849 -
T-Wave Alternans in Acute Myocardial Infarction: An Evaluation of the Time of Testing on Its Prognostic Accuracy
|
N/A | |
Active, not recruiting |
NCT03121183 -
Medico-economic Evaluation of Strategies for the Lead Extraction of Implantable Defibrillator and Pacemakers
|
N/A | |
Completed |
NCT02110004 -
Picasso NAV High-Density Mapping Catheter for Signal Analysis of Complex Arrhythmias - First-In-Man
|
Phase 1 | |
Completed |
NCT02045043 -
Genetic Risk Assessment of Defibrillator Events
|
N/A | |
Recruiting |
NCT01717469 -
Safety and the Effects of Isolated Left Ventricular Pacing in Patients With Bradyarrhythmias
|
Phase 4 | |
Completed |
NCT00919568 -
Monitoring Arrhythmia Patients (IMPACT)
|
N/A | |
Terminated |
NCT00124891 -
Study Evaluating GAP-486 in Non-sustained Ventricular Tachycardia
|
Phase 2 | |
Completed |
NCT02565069 -
Identification for the Treatment of Complex Arrhythmias
|
Phase 4 | |
Completed |
NCT03110146 -
EnSite Precision 2.1 Feasibility Study
|