Initial Management of Patients Receiving a Single Shock (IMPRESS) (IMPRESS)
Ventricular Tachycardia
About this trial
This is an interventional treatment trial for Ventricular Tachycardia focused on measuring tachycardia, defibrillator, arrythmia
Eligibility Criteria
Inclusion Criteria:
- 18-80 years old, both males and females
- Single or dual chamber ICD or BiVentricular ICD in situ
- Ischemic or non-ischemic cardiomyopathy
- Receive a single shock from their ICD for monomorphic ventricular tachycardia
Exclusion Criteria:
- ICD shock for polymorphic VT/VF or inappropriate shock
- Previous ventricular tachycardia ablation within 1 year
- NYHA Class IV heart failure or current inotrope therapy
- Ventricular tachycardia storm
- Listed for heart transplant or LVAD
- Pregnant as determined by urine pregnancy test prior to NIPS
Sites / Locations
- Saint Luke's Hospital of Kansas City
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Experimental
Other
Standard medical therapy
Ventricular Tachycardia Ablation
Negative NIPS/Non-intervention
Patients who have a positive NIPS study and are randomized to the medical therapy arm will either be initiated on antiarrhythmic therapy or will have their antiarrhythmic therapy intensified. All medication therapy is considered usual standard therapy.
Patients who have a positive NIPS study and are randomized to the ablation arm will undergo ventricular tachycardia ablation procedure guided by CardioInsight.
Patients who had a negative NIPS study will not be assigned to a treatment group and will be followed according to standard of care.