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Clinical Trial Summary

The intent of this observational study is to understand the role of non-invasive programmed stimulation (NIPS) to induce substrate based MMVT (Monomorphic Ventricular Tachycardia) in patients receiving new St. Jude Medical Implantable Cardioverter Defibrillator (ICD) or Cardiac Resynchronization Therapy Defibrillation (CRT-D) systems.


Clinical Trial Description

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

This study provides a mechanism for sites to refer subjects for potential enrollment to the Substrate Targeted Ablation Using the FlexAbilityâ„¢ Ablation Catheter System for the Reduction of Ventricular Tachycardia (STAR-VT) Investigational Device Exemption (IDE) study (ClinicalTrials.gov NCT02130765).

Patients receiving ICD or CRT-D device implant (or have received it within 30 days) may be enrolled in the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02584595
Study type Observational
Source Abbott Medical Devices
Contact
Status Withdrawn
Phase
Start date September 2015
Completion date February 2022

See also
  Status Clinical Trial Phase
Terminated NCT02130765 - Substrate Targeted Ablation Using the FlexAbilityâ„¢ Ablation Catheter System for the Reduction of Ventricular Tachycardia N/A
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Withdrawn NCT02216760 - Using Ripple Mapping to Guide Substrate Ablation of Scar Related Ventricular Tachycardia.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