Non-invasive Differentiation of Supraventricular Tachyarrhythmia
Recruiting · NCT06061120 · Observational (researchers observe without assigning treatment) · Lead sponsor: RWTH Aachen University
View the official record on ClinicalTrials.gov →Interventions studied
Recording of an extended high-resolution ECG
What this trial is about
1. Questionnaire for supraventricular tachycardia: About history and targeted diagnosis of supraventricular tachycardia 2. Extended Signal-averaged ECG for detailed P-Wave analysis and to calculate a virtual atrial electrocardiogram (ECG)
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- Scheduled for ablation of a supraventricular tachycardia (atrial fibrillation, typical atrial flutter, AV nodal reentry tachycardia, accessory pathway)
- majority
Exclusion criteria
- Unstable patient with need for intensive medical care
- Lack of language skills or limited cognitive abilities that prevent a differentiated anamnesis and information.
- Exclusion criteria for study section Questionnaire:
- \- Competing clinically present arrhythmias, including relevant supra- and ventricular extrasystole (\>5%/die).
- Exclusion criteria for study section Extended high-resolution ECG:
- Previous electrophysiological ablation at the same site for atrial fibrillation.
- Relevant supra- and ventricular extrasystole (\>5%/die).
- Other clinically present arrhythmias are not excluded if they can be sequentially triggered and ablated (e.g. atrial fibrillation and atrial flutter). Since separate detection is possible with the high-resolution ECG.
- Implanted active electrical device (e.g. pacemaker, defibrillator, deep brain pacemaker)
- Allergy to measuring electrodes
Where it is running
1 location listed.
- RWTH Aachen University - Aachen, North Rhine-Westphalia, Germany