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NCT06138873 · ClinicalTrials.gov registry record · NA
Ablation-Index Guided Scar-Mediated Ventricular Tachycardia Ablation in Patients With Ischemic Cardiomyopathy
A NA study of Ventricular Tachycardia and Ischemic Cardiomyopathy, sponsored by Rush University Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 5
- Study locations
NCT06138873: Recruiting NA study of Ventricular Tachycardia and Ischemic Cardiomyopathy, sponsored by Rush University Medical Center.
NCT06138873 is a NA study of Ventricular Tachycardia and Ischemic Cardiomyopathy that is actively recruiting participants, run by Rush University Medical Center. The registered enrollment target is 100 participants, below the 285-participant average among 28 other Ventricular Tachycardia trials with a reported enrollment target (65% lower). The trial reports 5 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06138873, a NA study of Ventricular Tachycardia and Ischemic Cardiomyopathy, is actively recruiting participants, sponsored by Rush University Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 5
- Study locations
Study Summary
Over the last decade, radiofrequency catheter ablation (RFCA) has become an established treatment for ventricular arrhythmias (VA). Due to the challenging nature of visualizing lesion formation in real time and ensuring an effective transmural lesion, different surrogate measures of lesion quality have been used. The Ablation Index (AI) is a variable incorporating power delivery in its formula and combining it with CF and time in a weighted equation which aims at allowing for a more precise estimation of lesion depth and quality when ablating VAs. AI guidance has previously been shown to improve outcomes in atrial and ventricular ablation in patients with premature ventricular complexes (PVC). However research on outcomes following AI-guidance for VT ablation specifically in patients with structural disease and prior myocardial infarction remains sparse. The investigators aim at conducting the first randomized controlled trial testing for the superiority of an AI-guided approach regarding procedural duration.
Primary Outcome
Percentage of reduction in ablation time in seconds, with ablation time defined as the total radiofrequency delivery time delivered during the VT ablation procedure. Total ablation time is automatically recorded by the Carto System Software and will be subsequently extracted as part of a raw unedited data file for unbiased endpoint evaluation.
Conditions Studied
Interventions
- PROCEDURE Ablation-index guided ventricular tachycardia ablation
- PROCEDURE Ventricular tachycardia ablation with no AI-guidance
Study Locations (5)
Illinois
- Rush University Medical Center - Chicago
Massachusetts
- Mass General Brigham and Women's Hospital - Boston
Michigan
- Medical University of Michigan - Ann Arbor
Minnesota
- Mayo Clinic - Rochester
South Carolina
- Medical University of South Carolina - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-10-23 |
| Est. Completion | 2027-11-23 |
| Phase | NA |
What NCT06138873 shows while recruiting
NCT06138873 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 285-participant average among 28 other Ventricular Tachycardia trials with a reported enrollment target (65% lower).
The record links to 2 conditions, with Ventricular Tachycardia appearing as the primary indexed condition, and to 2 interventions - of which Ablation-index guided ventricular tachycardia ablation is the first listed.
NCT06138873 lists 5 locations in 5 states (Illinois, Massachusetts, Michigan).
Frequently Asked Questions
What is clinical trial NCT06138873 about?
NCT06138873 is a clinical study titled "Ablation-Index Guided Scar-Mediated Ventricular Tachycardia Ablation in Patients With Ischemic Cardiomyopathy". Over the last decade, radiofrequency catheter ablation (RFCA) has become an established treatment for ventricular arrhythmias (VA). Due to the challenging nature of visualizing lesion formation in real time and ensuring an effective transmural lesion, different surrogate measures of lesion quality h...
What is the current status of trial NCT06138873?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-10-23. Estimated completion is 2027-11-23.
What conditions does trial NCT06138873 study?
This clinical trial studies the following conditions: Ventricular Tachycardia, Ischemic Cardiomyopathy.
What interventions are being tested in trial NCT06138873?
The interventions under investigation include: Ablation-index guided ventricular tachycardia ablation (PROCEDURE), Ventricular tachycardia ablation with no AI-guidance (PROCEDURE).
Who is sponsoring clinical trial NCT06138873?
This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06138873 being conducted?
This trial has 5 study locations across Illinois, Massachusetts, Michigan, Minnesota, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Ventricular Tachycardia
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06138873's enrollment target sits among peer trials
100 16th of 28 higher than 12 of 28 other Ventricular Tachycardia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Ventricular Tachycardia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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