Atrial Tachycardia Clinical Trials

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

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Germany
Vivantes Klinikum Am Urban Berlin
RECRUITING
Berlin
Evangelic Hospital Düsseldorf
RECRUITING
Düsseldorf
Evangelic Hospital Hagen-Haspe
RECRUITING
Hagen
Asklepios St. Georg
RECRUITING
Hamburg
Städtisches Klinikum Karlsruhe
RECRUITING
Karlsruhe
Universitätsklinikum Schleswig Holstein
RECRUITING
Kiel
Contact Information
Primary
Christian Meyer, MD
christian.meyer@evk-duesseldorf.de
00492119191855
Time Frame
Start Date: 2020-12-22
Estimated Completion Date: 2027-06
Participants
Target number of participants: 100
Treatments
Experimental: Standard approach
Patients will receive a standard approach for ablation of atrial tachycardia.
Experimental: Minimalized approach
Patients will receive a minimalized approach for ablation of atrial tachycardia.
Authors
Camerer Cornelia
Sponsors
Leads: Evangelical Hospital Düsseldorf

This content was sourced from clinicaltrials.gov