Radiation Therapy for Ventricular Tachycardia
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new approach to treating ventricular tachycardia (VT), a heart condition that causes dangerously fast heartbeats. Researchers aim to determine the lowest safe dose of radiation therapy (cardiac radioablation) needed to treat VT effectively. Participants will receive varying radiation doses to identify the most effective one. Individuals who have had a heart attack, experience frequent VT episodes despite medication, and have tried other treatments might be suitable candidates. As an unphased trial, this study provides an opportunity to contribute to groundbreaking research that could lead to new treatment options for VT.
Do I need to stop my current medications for the trial?
The trial protocol does not specify whether you need to stop taking your current medications. However, since the trial involves participants with ventricular tachycardia that is not controlled by medications, it is likely that you will continue your current medications.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that cardiac radioablation, a type of radiation therapy, is generally well-tolerated for treating ventricular tachycardia (VT), a serious heart rhythm problem. One study found that patients experienced fewer VT episodes after this treatment, effectively reducing the occurrence of this dangerous heart rhythm.
Regarding safety, several large studies have confirmed that stereotactic radiation therapy, a precise form of radiation treatment, is safe for patients with recurring VT. These studies indicate that patients usually do not experience severe side effects from the treatment.
While there is no absolute guarantee of zero side effects, these findings are promising. They suggest that cardiac radioablation is a safe option for those dealing with hard-to-treat VT. A thorough discussion with a healthcare provider is essential to understand the potential risks and benefits before joining a trial.12345Why are researchers excited about this trial?
Researchers are excited about cardiac radioablation for ventricular tachycardia because it offers a non-invasive alternative to the standard of care treatments like antiarrhythmic drugs and catheter ablation. Unlike these traditional methods, which can involve surgery or long-term medication use, cardiac radioablation uses targeted radiation therapy, which can be precisely delivered to the heart tissue causing the arrhythmia. This innovative approach has the potential to reduce procedural risks and recovery time. Additionally, different radiation doses—15 Gy, 20 Gy, and 25 Gy—are being explored to determine the most effective and safe option, which could lead to personalized treatment plans.
What evidence suggests that this trial's treatments could be effective for ventricular tachycardia?
Research has shown that cardiac radioablation is a promising treatment for ventricular tachycardia (VT), especially for patients unresponsive to other treatments. This trial will compare different doses of radiation therapy—15 Gy, 20 Gy, and 25 Gy—to evaluate their effectiveness and safety. One study found that this approach can greatly reduce VT episodes. Another analysis showed that this method has moderate side effects and is reasonably safe. Specifically, a key trial found that radiation therapy effectively decreased the number of VT episodes and the need for medication. Overall, cardiac radioablation offers a potential new option for those dealing with severe heart rhythm problems.13467
Who Is on the Research Team?
John M. Robertson
Principal Investigator
Corewell Health William Beaumont University Hospital
Are You a Good Fit for This Trial?
This trial is for adults who've had a heart attack and suffer from ventricular tachycardia (VT), which hasn't improved after at least one cardiac ablation. They must have an implanted defibrillator, not be pregnant or breastfeeding if of reproductive age, and should not have severe heart failure or prior chest radiation.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Radiation Therapy
Participants receive cardiac radioablation with varying doses (15 Gy, 20 Gy, or 25 Gy) to determine the minimum effective dose
Observation and Evaluation
Participants are observed for dose limiting toxicity and efficacy, with a 6-week blanking period followed by 8 weeks of evaluation
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Cardiac Radioablation
Find a Clinic Near You
Who Is Running the Clinical Trial?
William Beaumont Hospitals
Lead Sponsor