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Initial Management of Patients Receiving a Single Shock (IMPRESS) (IMPRESS)

Primary Purpose

Ventricular Tachycardia

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ventricular Tachycardia Ablation
Standard Medical Therapy
Non-Invasive Programmed Stimulation (NIPS)
Sponsored by
Saint Luke's Health System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ventricular Tachycardia focused on measuring tachycardia, defibrillator, arrythmia

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Experimental

Other

Arm Label

Standard medical therapy

Ventricular Tachycardia Ablation

Negative NIPS/Non-intervention

Arm Description

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.

Outcomes

Primary Outcome Measures

ICD Shocks
Number of recurrent ICD shocks

Secondary Outcome Measures

Total Mortality
Number of related deaths
Hospitalizations
Number of related hospitalizations
ATP Therapy as recorded by ICD
Number of ATP therapies administered by ICD
Non-sustained VT
Initiation of antiarrythmic medication
Number of times new medical therapy was started as documented in the medical record
Modification of antiarrythmic medication
Number of times medical therapy was changed
Repeat ablation
Number of repeat ablation procedures

Full Information

First Posted
April 25, 2018
Last Updated
April 11, 2023
Sponsor
Saint Luke's Health System
Collaborators
Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT03531502
Brief Title
Initial Management of Patients Receiving a Single Shock (IMPRESS)
Acronym
IMPRESS
Official Title
Initial Management of Patients Receiving a Single Shock (IMPRESS)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Terminated
Why Stopped
lack of funding
Study Start Date
April 9, 2018 (Actual)
Primary Completion Date
April 4, 2023 (Actual)
Study Completion Date
April 4, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Saint Luke's Health System
Collaborators
Medtronic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to determine the optimal treatment for patients who receive a single shock from their implantable cardioverter defibrillator (ICD). All participants in this study will be fitted with a special electrode vest to detect the origin of heart rhythm abnormalities and then they will undergo a procedure called Non-Invasive Programmed Stimulation (NIPS). This procedure involves sedating a participants with anesthesia and then using the participant's own ICD to try to stimulate the heart to go into ventricular tachycardia. If this procedure is unable to induce the participant into ventricular tachycardia, then the participant will just be managed with usual care and will not be placed on any additional medications and will not undergo an ablation. However, if the NIPS induces the ventricular tachycardia, the electrode vest will be used to determine the origin of the abnormal heart rhythm inside the heart. After a successful NIPS procedure, the participants will be randomly assigned to either be placed on medication therapy or undergo catheter ablation. The outcomes from all three groups will be compared and the researchers hope to better understand which participants are most likely to benefit from watchful waiting versus medication versus catheter ablation.
Detailed Description
Patients with a history of ventricular tachycardia requiring defibrillation or who are at risk for developing ventricular tachycardia will undergo placement of an implantable cardioverter defibrillator (ICD) for purposes of prevention of sudden cardiac arrest. While the ICD is lifesaving, if a patient receives a shock from their ICD it is painful and the entire experience is very traumatic. Traditionally, the management of these patients who receive a single shock from their ICD is variable because it is not known if the patient will continue to experience further shocks or not. Some physicians will initiate antiarrhythmic medical therapy after only a single shock, whereas others will wait until the patient has recurrent ICD shocks before initiating therapy. All patients should be counseled to not drive for 6 months following a shock. Ventricular tachycardia ablation, a procedure involving placing catheters from the groin into the chambers of the heart to isolate the source of ventricular tachycardia and eliminate these foci through delivery of radiofrequency energy, is typically reserved for patients with multiple recurrent cases of ventricular tachycardia. While some studies have shown that ventricular tachycardia ablations can be done safely at an earlier course of the disease and this procedure has been demonstrated to reduce further ICD shocks, this practice is not commonplace. Patients who undergo a ventricular tachycardia ablation procedure, will initially have catheters placed into the ventricular chambers of the heart and these catheters will be used to stimulate the heart in an attempt to induce the ventricular tachycardia, a process known as programmed stimulation. One major limitation of a ventricular tachycardia ablation procedure is the need to be able to induce the ventricular tachycardia rhythm via programmed stimulation. If this rhythm cannot be induced then it is very difficult to perform the ventricular tachycardia ablation procedure. Non-invasive programmed stimulation (NIPS) is a means of performing programmed stimulation using the patient's own ICD and does not involve placing catheters into the heart. Aim: The aim of this study is to investigate if non-invasive programmed stimulation (NIPS) can be used to risk stratify patients determine if earlier intervention with either antiarrhythmic medications or ablation in patients with recurrent ventricular tachycardia that received ICD shocks would help decrease further ICD shocks and hospitalizations for ventricular arrhythmias. Primary hypothesis: Patients receiving a single ICD shock for ventricular tachycardia who undergo a non-invasive programmed stimulation (NIPS) that fails to induce any sustained ventricular tachycardia, are at low likelihood of experiencing recurrent ICD shocks within the next year. Secondary hypothesis: For patients receiving a single ICD shock for ventricular tachycardia who undergo non-invasive programmed stimulation (NIPS) that induces a sustained, monomorphic ventricular tachycardia rhythm, the performance of ventricular tachycardia ablation will reduce the incidence of recurrent ICD shocks within the next year, as compared to antiarrhythmic therapy alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventricular Tachycardia
Keywords
tachycardia, defibrillator, arrythmia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective, randomized, controlled
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard medical therapy
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Ventricular Tachycardia Ablation
Arm Type
Experimental
Arm Description
Patients who have a positive NIPS study and are randomized to the ablation arm will undergo ventricular tachycardia ablation procedure guided by CardioInsight.
Arm Title
Negative NIPS/Non-intervention
Arm Type
Other
Arm Description
Patients who had a negative NIPS study will not be assigned to a treatment group and will be followed according to standard of care.
Intervention Type
Procedure
Intervention Name(s)
Ventricular Tachycardia Ablation
Intervention Description
Ventricular Tachycardia Ablation
Intervention Type
Other
Intervention Name(s)
Standard Medical Therapy
Intervention Description
For the antiarrhythmic naïve patients, the attending physician may initiate therapy with sotalol or amiodarone. For patients already on therapy with sotalol or amiodarone, the attending physician may choose to either increase the dosage/ frequency of these medications and/or add mexiletine to the regimen. Other alterations to medical therapy, such as adjusting the dose of beta-blockers, calcium-channel blockers, anti-hypertensive, diuretic or anti-anginal medications may be performed at the discretion of the attending physician.
Intervention Type
Procedure
Intervention Name(s)
Non-Invasive Programmed Stimulation (NIPS)
Intervention Description
All patients will receive this procedure in attempt to induce ventricular tachycardia. The outcome of this procedure determines if a patient will be randomized.
Primary Outcome Measure Information:
Title
ICD Shocks
Description
Number of recurrent ICD shocks
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Total Mortality
Description
Number of related deaths
Time Frame
12 months
Title
Hospitalizations
Description
Number of related hospitalizations
Time Frame
12 months
Title
ATP Therapy as recorded by ICD
Description
Number of ATP therapies administered by ICD
Time Frame
12 months
Title
Non-sustained VT
Time Frame
12 months
Title
Initiation of antiarrythmic medication
Description
Number of times new medical therapy was started as documented in the medical record
Time Frame
12 months
Title
Modification of antiarrythmic medication
Description
Number of times medical therapy was changed
Time Frame
12 months
Title
Repeat ablation
Description
Number of repeat ablation procedures
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sanjaya Gupta, MD
Organizational Affiliation
Saint Luke's Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saint Luke's Hospital of Kansas City
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18160685
Citation
Reddy VY, Reynolds MR, Neuzil P, Richardson AW, Taborsky M, Jongnarangsin K, Kralovec S, Sediva L, Ruskin JN, Josephson ME. Prophylactic catheter ablation for the prevention of defibrillator therapy. N Engl J Med. 2007 Dec 27;357(26):2657-65. doi: 10.1056/NEJMoa065457.
Results Reference
result
PubMed Identifier
27149033
Citation
Sapp JL, Wells GA, Parkash R, Stevenson WG, Blier L, Sarrazin JF, Thibault B, Rivard L, Gula L, Leong-Sit P, Essebag V, Nery PB, Tung SK, Raymond JM, Sterns LD, Veenhuyzen GD, Healey JS, Redfearn D, Roux JF, Tang AS. Ventricular Tachycardia Ablation versus Escalation of Antiarrhythmic Drugs. N Engl J Med. 2016 Jul 14;375(2):111-21. doi: 10.1056/NEJMoa1513614. Epub 2016 May 5.
Results Reference
result
PubMed Identifier
22516442
Citation
Frankel DS, Mountantonakis SE, Zado ES, Anter E, Bala R, Cooper JM, Deo R, Dixit S, Epstein AE, Garcia FC, Gerstenfeld EP, Hutchinson MD, Lin D, Patel VV, Riley MP, Robinson MR, Tzou WS, Verdino RJ, Callans DJ, Marchlinski FE. Noninvasive programmed ventricular stimulation early after ventricular tachycardia ablation to predict risk of late recurrence. J Am Coll Cardiol. 2012 Apr 24;59(17):1529-35. doi: 10.1016/j.jacc.2012.01.026.
Results Reference
result
PubMed Identifier
31698933
Citation
Kheiri B, Barbarawi M, Zayed Y, Hicks M, Osman M, Rashdan L, Kyi HH, Bachuwa G, Hassan M, Stecker EC, Nazer B, Bhatt DL. Antiarrhythmic Drugs or Catheter Ablation in the Management of Ventricular Tachyarrhythmias in Patients With Implantable Cardioverter-Defibrillators: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Circ Arrhythm Electrophysiol. 2019 Nov;12(11):e007600. doi: 10.1161/CIRCEP.119.007600. Epub 2019 Nov 8.
Results Reference
derived

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Initial Management of Patients Receiving a Single Shock (IMPRESS)

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