Registry for managing outcomes in patients with ventricular tachycardia
MANAGEment of Ventricular Tachycardia Outcomes Registry
This study collects information from patients with ventricular tachycardia to see how different factors affect their treatment and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 130 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | CorVita Science Foundation Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Trial ID | NCT06455488 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this registry are adults aged 18 and older who have been diagnosed with ventricular tachycardia.
Not a fit: Patients under 18 years old or those without a diagnosis of ventricular tachycardia may not benefit from this registry.
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 performed: Other registries focusing on arrhythmias have shown success in improving patient outcomes, indicating that this approach may also be beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Must be at least 18 years old * Must not be Exclusion Criteria: \-
Where this trial is running
Chicago, Illinois
- Corvita Science Foundation — Chicago, Illinois, United States (Recruiting)
Study contacts
- Study coordinator: Martin C Burke, DO
- Email: mburke@corvitahealth.org
- Phone: 7735208322
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.