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RecruitingNCT06455488MANAGE-VTUpdated Jun 12, 2024

MANAGE-VT Registry - MANAGEment of Ventricular Tachycardia Outcomes Registry

An observational study in Ventricular Tachycardia, sponsored by CorVita Science Foundation. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-12.

Sponsored by CorVita Science Foundation · Observational

From the registry’s dates

  • Started Jul 2020; still recruiting 6 years 2 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
130
Ages
18 Years and older
Sex
All
01

Study summary

Data collection registry for patients with ventricular tachycardia to help physicians give better care for patients clinically and procedurally.

Read the detailed description

After consent from a patient the research team will input patients data from many different categories. There is a link to the PDF for the consent form, a patients anticoagulant medications will be assessed, their ventricular tachycardia (VT) history will be inputted, and their date of birth and zip code will inputted. The research team will then input any EKG's, echocardiograms, VT ablations, ICD's, S-ICD's, lab results, and comorbidities.

02

Conditions studied

  • Ventricular Tachycardia

Keywords

  • ventricular arrhythmia
  • ventricular tachycardia
  • ventricular fibrillation
  • stroke
03

In context

Tachycardia

623 studies on the registry are indexed under Tachycardia; 81 are open to participants now.

This study's planned enrollment of 130 is below the median of 149 across 208 observational studies indexed under Tachycardia.

Browse Tachycardia studies →

Lead sponsor

CorVita Science Foundation is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

All patients who have been diagnosed and have evidence of ventricular tachycardia and are over the age of 18. Every patient was presented with a consent form and was given a description of the study in a clinical setting.

Inclusion criteria

  • Must be at least 18 years old
  • Must not be

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
130 participants (estimated)
Patient registry
No

Groups and cohorts

  • MANAGE-VT Patients

    Patients will be assessed on the status of their ventricular tachycardia as well as other criteria such as: EKG,

    Procedure: Ventricular Tachycardia Ablation · Device: ICD Implant · Drug: Antiarrhythmic drug · Diagnostic Test: EKG · Diagnostic Test: Cardioversion · Diagnostic Test: Echocardiogram

Interventions

  • ProcedureVentricular Tachycardia Ablation

    This is a surgical ablation meant to reset patients irregular rhythm back to sinus.

  • DeviceICD Implant

    A pacemaker or defibrillator implant to prevent SCD

    Also known as: Pacemaker Implant

  • DrugAntiarrhythmic drug

    Drug therapies

    Also known as: Statin Therapy, Anticoagulants

  • Diagnostic testEKG

    Monitoring EKG testing done on registry patients

  • Diagnostic testCardioversion

    Monitoring cardioversions on registry patients

  • Diagnostic testEchocardiogram

    Monitoring echocardiogram testing done on patients

06

What researchers measure

Primary outcomes

  1. Recurrence of Ventricular Tachycardia

    The natural progression of v-tach will be assessed through medical record review

    Time frame: July 20, 2020 - Present

  2. Number of Participants with Risk of Sudden Cardiac Death

    All events of sudden cardiac death that arise from patients with ventricular tachycardia

    Time frame: July 20, 2020 - Present

  3. Prevent Risk of Stroke

    All strokes, transient ischemic and systemic thrombo-embolic events

    Time frame: July 20, 2020 - Present

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06455488
Lead sponsor
CorVita Science Foundation
Responsible party
Sponsor
First posted
Jun 12, 2024
Start date
Jul 20, 2020
Primary completion
Jul 20, 2030 (estimated)
Completion
Jul 20, 2030 (estimated)
Last update
Jun 12, 2024

Study contacts

Martin C Burke, DO
Contact
mburke@corvitahealth.org
7735208322
Edward M Burke
Contact
eddie@corvitahealth.org
7737297956

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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