Cardiac Radioablation for VT
Part of paid clinical trials in Royal Oak, Michigan.
- Sponsor
- Corewell Health East
- Study ID
- NCT06593418
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Myocardial Infarction
- Ventricular Tachycardia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Stereotactic Body Radiation Therapy (SBRT) — RADIATIONStereotactic body radiation therapy, which delivers precise, high-dose radiation non-invasively to generate thermal scarring to myocardial targets causing VT
Study Details
The goal of this interventional study is to determine the minimum dose necessary for successful cardiac radioablation of refractory ventricular tachycardia (VT) and to study the utility of target volume definition using Delayed Enhancement Cardiac MRI (DE-CMR) .
Key Dates
- Start date
- Jul 31, 2026
- Status verified
- Apr 2026
- Primary completion
- Jan 31, 2028
- Completion
- Jan 31, 2028
Study Design
- Enrollment
- 24 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Radiation Therapy at 15 Gy for Ventricular TachycardiaPost myocardial infarction patients with refractory ventricular tachycardia requiring cardio ablation, treated with 15 Gy
- Experimental: Radiation Therapy at 20 Gy for Ventricular TachycardiaPost myocardial infarction patients with refractory ventricular tachycardia requiring cardio ablation, treated with 20 Gy
- Experimental: Radiation Therapy at 25 Gy for Ventricular TachycardiaPost myocardial infarction patients with refractory ventricular tachycardia requiring cardio ablation, treated with 25 Gy
Primary Outcome Measure
Change in number of ventricular tachycardia (VT) episodes from pre-cardiac radioablation to post-cardiac radioablation [ Time Frame: 56 days pre-treatment and 98 days post treatment (42 day blanking period plus 56 days) ]
Central Contacts
- John Roberston, MD248-551-7038
- Kristen Grant, RN248-551-0439
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Corewell Health William Beaumont University Hospital | Royal Oak | Michigan | 48073 |
Find similar trials in Royal Oak, MI
Related Studies
- IVTCC 2.0: A Prospective Multicenter Ventricular Tachycardia Catheter Ablation RegistryEnrolling By Invitation · University of California, Los Angeles · Phoenix, Arizona
- Improving Cardiac Rehabilitation Exercise Using Target Heart Rate TrialPHASE2 · Recruiting · Baystate Medical Center · Springfield, Massachusetts
- MCNAIR Study: coMparative effeCtiveness of iN-person and teleheAlth cardIac RehabilitationRecruiting · University of California, San Francisco · San Francisco, California
- Ablation-Index Guided Scar-Mediated Ventricular Tachycardia Ablation in Patients With Ischemic CardiomyopathyRecruiting · Rush University Medical Center · Chicago, Illinois