Insights from atrial surface activation throughout atrial tachycardia cycle length: A new mapping tool.
Masateru Takigawa, Claire A Martin, Nicolas Derval...
https://pubmed.ncbi.nlm.nih.gov/31004777/Actively Recruiting
Led by Evangelical Hospital Düsseldorf · Updated on 2026-04-30
100
Participants Needed
6
Research Sites
N/A
Total Duration
Researchers are studying atrial tachycardia AT that occurs after ablation of atrial fibrillation AF or cardiac surgery. This condition is difficult to treat due to the complex nature of the heart tissue and the mechanisms causing AT. The study aims to compare two methods of catheter ablation for ATstandard versus minimalized approachesto see which leads to better arrhythmia-free survival. The trial is prospective, randomized, and conducted at multiple centers to improve understanding using new ultra-high-density mapping techniques. Participants will receive catheter-based ablation using radiofrequency to treat their AT. They will be randomly assigned to either a standard ablation approach or a minimalized ablation approach targeting the clinical AT. The study will evaluate various procedural details such as procedure duration, fluoroscopy time, radiofrequency application time, ablated heart area, and the number of blocked lines. Both groups will be monitored during the procedure with advanced mapping techniques to assess the underlying heart substrate and AT mechanisms. During the study, participants will undergo assessments including ECG documentation of AT, intraprocedural mapping, and evaluations of arrhythmia recurrence over one year. Researchers will measure the recurrence of sustained arrhythmia lasting more than 30 seconds as the primary outcome after one year. Other measures include inducibility of AT after ablation, predictability of secondary AT from mapping, and procedure-related parameters. Participants will be followed for safety and treatment effectiveness throughout the study period, which started in December 2020 and is expected to continue until June 2027.
CONDITIONS
Ablation of Consecutive Atrial Tachycardia
C
Christian Meyer, MD
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Evangelical Hospital Düsseldorf
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single procedure day
Participants undergo catheter ablation using either a standard or a minimalized approach to treat atrial tachycardia.
1 procedure visit (in-person)
Duration - Up to 1 year
Participants are monitored for recurrence of arrhythmia and other outcomes for up to 1 year after the ablation procedure.
Periodic follow-up visits over 1 year
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Masateru Takigawa, Claire A Martin, Nicolas Derval...
https://pubmed.ncbi.nlm.nih.gov/31004777/Christian Meyer, Ann-Kathrin Kahle, Nikolaos Dagres...
https://pubmed.ncbi.nlm.nih.gov/41435855/Christian Meyer
https://pubmed.ncbi.nlm.nih.gov/31400216/Christiane Jungen, Ruken Akbulak, Ann-Kathrin Kahle...
https://pubmed.ncbi.nlm.nih.gov/32748442/Nicolas Derval, Masateru Takigawa, Antonio Frontera...
https://pubmed.ncbi.nlm.nih.gov/32703564/Evangelical Hospital Düsseldorf
Lead Sponsor