Modification of the Local Abnormal Ventricular Activity Only
NCT ID: NCT05331716
Last Updated: 2022-10-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
22 participants
OBSERVATIONAL
2019-01-01
2021-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Catheter Ablation for Nonsustained Ventricular Tachycardia in Patients With Ischemic Cardiomyopathy
NCT03147027
Ventricular Tachycardia Ablation in LVAD Patients
NCT06063811
R Wave Sensing After VT Ablation
NCT03779165
Endo- and Epicardial vs. Endocardial Ablation of Ventricular Tachycardia in Patients With Cardiac Disease
NCT01767220
Effect of Multielectrode Versus Point-by-Point Mapping on Recurrence of Ventricular Tachycardia in Ischemic Heart Disease
NCT05203484
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Cardiac ablation therapy
In a subset of patients with known therapy refractory arrhythmia sole LAVA modification is fashioned
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Krankenhaus Landshut Achdorf
UNKNOWN
University of Kiel
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Prof. Dr. Hendrik Bonnemeier
Coordinating principal investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Hendrik Bonnemeier, PhD
Role: STUDY_DIRECTOR
University of Kiel - Medical Faculty
Stefan Borov, MD
Role: PRINCIPAL_INVESTIGATOR
University of Kiel - Medical Faculty
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Krankenhaus Landshut Achdorf
Landshut, Bavaria, Germany
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2021-1232
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.