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Clinical Trials/NCT05239364
NCT05239364RecruitingNot Applicable

Ablation of CONseCutive atriaL Tachycardia gUided by Ultra-high-DEnsity Mapping

Evangelical Hospital Düsseldorf5 sites in 1 country100 target enrollmentStarted: December 22, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
100
Locations
5
Primary Endpoint
Recurrence of any sustained arrhythmia (>30 sec.)

Study Overview

Brief Summary

Ablation of consecutive atrial tachycardia (AT) after ablation of atrial fibrillation (AF) or cardiac surgery can be challenging due to complex substrate and AT mechanisms. A substantial portion of patients is known to show various tachycardias and recurrences occur in a noticeable number of cases. With the availability of novel ultra-high-density mapping techniques characterization and understanding of AT mechanisms and underlying substrate can be improved. Aim of this prospective, multi-center, randomized study is to compare a standard AT ablation approach versus minimalized ablation of the clinical AT in regards to arrhythmia free survival.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Consecutive AT subsequent to prior AF ablation procedure or cardiac surgery
  • Surface ECG-documentation of AT as primary clinical arrhythmia
  • ECG indicating stable, map-able AT (stable activation sequence, and CL stability) with cycle length ≥ 200ms

Exclusion Criteria

  • < 18 years
  • No previous atrial fibrillation ablation procedure or cardiac surgery
  • Pregnant women or women of childbearing potential without a negative pregnancy test within 48 hours prior to treatment
  • History of hemorrhagic diathesis or other coagulopathies
  • Contraindications for oral anticoagulation
  • Hyper- or hypothyroidism
  • Has any condition that would make participation not be in the best interest of the subject

Outcomes

Primary Outcomes

Recurrence of any sustained arrhythmia (>30 sec.)

Time Frame: 1 year

Secondary Outcomes

  • Inducibility of atrial tachycardia (AT) after ablation of clinical/primary AT (partial success)(Intraprocedural)
  • Area of low voltage in sinus map (cm2)(Intraprocedural)
  • Total radiofrequency application time(intraprocedural)
  • Fluoroscopy time(intraprocedural)
  • Number of blocked lines(intraprocedural)
  • Predictability of secondary AT by analysis of clinical AT map and voltage map(Intraprocedural)
  • Procedure duration time(Intraprocedural)
  • Ablated area (cm2)(intraprocedural)

Investigators

Sponsor
Evangelical Hospital Düsseldorf
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Christian Meyer

Prof. Dr. Christian Meyer

Evangelical Hospital Düsseldorf

Study Sites (5)

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