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Clinical Trial Summary

To demonstrate that scar-based ventricular tachycardia (VT) ablation using the FlexAbility™ 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.


Clinical Trial Description

Approximately 50 centers in the United States (US) will participate in the study. Additional centers outside the US may be considered, as necessary. The anticipated enrollment duration is 48-60 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02130765
Study type Interventional
Source Abbott Medical Devices
Contact
Status Terminated
Phase N/A
Start date November 2014
Completion date July 25, 2016

See also
  Status Clinical Trial Phase
Withdrawn NCT02584595 - Evaluation of Inducible Monomorphic Ventricular Tachycardia (MMVT) in Patients With St. Jude Medical (SJM) Implantable Cardioverter Defibrillator (ICD) Systems or Cardiac Resynchronization Therapy Defibrillation (CRT-D) Systems.
Active, not recruiting NCT04893317 - Cryoablation for Monomorphic Ventricular Tachycardia (CryoCure-VT) N/A
Completed NCT03734562 - Trial to Evaluate the Efficacy and Safety of Substrate Ablation of Monomorphic Ventricular Tachycardia N/A
Withdrawn NCT02216760 - Using Ripple Mapping to Guide Substrate Ablation of Scar Related Ventricular Tachycardia. N/A