Registry for managing outcomes in patients with ventricular tachycardia
Official title: MANAGEment of Ventricular Tachycardia Outcomes Registry
Run by CorVita Science Foundation · NCT06455488 · Data updated 2026-11-12
This study collects information from patients with ventricular tachycardia to see how different factors affect their treatment and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 130 (estimated) |
| Sponsor | CorVita Science Foundation Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Status | Recruiting |
| Started | July 20, 2020 |
| Main results expected | July 20, 2030 |
| Study ends | July 20, 2030 |
| Registry record updated | June 12, 2024 |
| Trial ID | NCT06455488 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this registry are adults aged 18 and older who have been diagnosed with ventricular tachycardia.
✕Probably not a fit
Patients under 18 years old or those without a diagnosis of ventricular tachycardia may not benefit from this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This registry collects data from patients diagnosed with ventricular tachycardia to enhance clinical care and procedural outcomes. After obtaining consent, the research team gathers comprehensive patient information, including medical history, anticoagulant medications, and diagnostic results such as EKGs and echocardiograms. The goal is to create a robust database that can inform better treatment strategies for ventricular tachycardia. This observational approach allows for the analysis of various factors affecting patient outcomes.
Why it matters
Potential benefit: If successful, this registry could lead to improved management and treatment strategies for patients with ventricular tachycardia.
How similar studies have gone: Other registries focusing on arrhythmias have shown success in improving patient outcomes, indicating that this approach may also be beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Must be at least 18 years old * Must not be Exclusion Criteria: \-
Where it's running
-
Corvita Science Foundation
Chicago, Illinois, United States Recruiting
Study contacts
- Study coordinator: Martin C Burke, DO
- Email: mburke@corvitahealth.org
- Phone: 7735208322
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Parasternal EV-ICD System Pivotal Study
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Real-time intracardiac ultrasound to guide ablation of ventricular arrhythmias
It tests whether using ultrasound inside the heart during PVC or VT ablation can reduce X-ray exposure for adults having these procedures.
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Arrhythmia mapping with a paddle-shaped multi-electrode catheter
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.