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Trial · NCT07896980

MRI-guided Ventricular Tachycardia Ablation in Patients With Structural Heart Disease

NCT07896980, Not applicable, Not yet recruiting, China National Center for Cardiovascular Diseases

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. MRI-guided Ventricular Tachycardia Ablation in Patients With Structural Heart Disease. Trials, record NCT07896980. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896980

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
MRI-guided Ventricular Tachycardia Ablation in Patients With Structural Heart Disease
NCT number
NCT07896980
Status
Not yet recruiting
Phases
Not applicable
Enrollment
526 participants, estimated
Lead sponsor
China National Center for Cardiovascular Diseases
Conditions
Ventricular Tachycardia (VT), Ischemic Cardiomyopathy, Non-ischemic Cardiomyopathy
Interventions
LGE-MRI-integrated EAM-guided catheter ablation, Conventional EAM-guided catheter ablation
First posted
2026-10-27
Last updated
2026-10-27

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryComposite of ventricular tachycardia recurrence, cardiovascular hospitalization, or death12 months after the ablation procedure
VT recurrence is defined as any appropriate ICD therapy (shock or antitachycardia pacing) or documented sustained monomorphic VT lasting more than 30 seconds. Cardiovascular hospitalization is defined as hospital admission after the randomly assigned procedure due to heart failure, procedure-associated complications, or arrhythmic causes.
SecondaryVentricular tachycardia recurrence rate at 6 months6 months after the ablation procedureProportion of patients with recurrent VT, defined as any appropriate ICD therapy (shock or antitachycardia pacing) or documented sustained monomorphic VT lasting more than 30 seconds.
SecondaryOutcomes of the LGE-negative ablation registry cohort compared with the randomized patients12 months after the ablation procedure
Prespecified comparison of the composite of VT recurrence, cardiovascular hospitalization, or death between the prospective observational registry of LGE-negative patients undergoing ablation and the randomly assigned (LGE-positive) patients.
SecondaryIncidence of ablation-related complicationsWithin 7 days after the ablation procedureIncidence of procedure-related adverse events, including pericardial tamponade, pericardial effusion, cardiac perforation, esophageal fistula, and thromboembolism.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers12

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
25091404BACKGROUNDPubMed
26324538BACKGROUNDPubMed
28688990BACKGROUNDPubMed
29018519BACKGROUNDPubMed
29255125BACKGROUNDPubMed
29584897BACKGROUNDPubMed
31075787BACKGROUNDPubMed
35210090BACKGROUNDPubMed
35507499BACKGROUNDPubMed
36017572BACKGROUNDPubMed

1 to 10 of 12

See all 12 papers

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07896980

GET https://conductscience.org/api/trials/v1/NCT07896980/registered