Study to Verify Proper Detection of Supraventricular Tachyarrhythmia With Single-Lead Dual-Chamber Implantable Cardioverter-Defibrillators (ADRIA)
- Conditions
- Tachyarrhythmia
- Registration Number
- NCT00324662
- Lead Sponsor
- Biotronik SE & Co. KG
- Brief Summary
A unique single-lead dual-chamber implantable cardioverter-defibrillator (ICD) system (produced by Biotronik, Germany) features a conventional electrode in the ventricle (anchored in the ventricular apex) and a floating electrode (ring on the lead body) in the atrium, capable of sensing atrial electrical signals. The purpose of this study is to determine whether this system detects a supraventricular tachyarrhythmia (e.g. atrial fibrillation, atrial tachycardia) in the equivalent manner as conventional dual-lead dual-chamber ICDs using two separate electrodes anchored in the ventricle and in the atrium, respectively.
- Detailed Description
Supraventricular tachyarrhythmia (SVT) is the main cause of inappropriate therapy in patients with single-chamber implantable cardioverter-defibrillators (ICDs). To minimize inappropriate shock delivery, ICDs should sense both atrial and ventricular intracardiac signals. Dual-chamber ICDs are used for this purpose, but are associated with increased postoperative complications due to the implantation of a separate atrial lead. It has to be shown that a novel single-lead dual-chamber ICD-system with enhanced SVT discrimination can achieve the same specificity in discriminating SVT episodes as conventional dual-chamber ICD, without the disadvantage of the implantation of several leads. In this study patients eligible for dual-chamber ICD therapy who do not need atrial pacing will receive either a single-lead dual-chamber ICD (Belos A+ and Kainox A+ electrode) or a dual-lead dual-chamber ICD (Belos DR). SMART detection algorithm will be used in both study groups for discrimination between atrial and ventricular tachyarrhythmias. Atrial tachyarrhythmia episodes are facultatively induced in both groups at implantation or predischarge via a bipolar stimulation catheter. Induced episodes and the corresponding ICD intervention (detection and therapy or inhibition of therapy) are documented. Follow-ups are scheduled for 1, 3, 6 and 12 months after implantation. ICD intervention, particularly related to spontaneous SVT episodes, will be evaluated based on ICD diagnostic memory data interrogated at follow-up controls.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 260
- ICD indication according to American College of Cardiology/American Heart Association (ACC/AHA) guidelines.
- Informed consent
- Permanent atrial fibrillation
- Requirement for atrial pacing
- Patient is underage
- No signed patient agreement
- Patient life expectancy under 6 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Rate of correctly discriminated supraventricular tachyarrhythmia episodes (specificity)
- Secondary Outcome Measures
Name Time Method Complication rate (e.g. lead dislocation, lead fracture) Duration of implantation Electrode performance (P-/R-wave amplitudes, ventricular pacing threshold and impedance) Sensitivity (rate of correctly discriminated episodes of ventricular fibrillation or ventricular tachycardia)
Trial Locations
- Locations (10)
Kantonspital Basel, Abteilung für Kardiologie
🇨🇭Basel, Switzerland
Medizinische Hochschule Hannover
🇩🇪Hannover, Germany
Sana Klinikum Lichtenberg
🇩🇪Berlin, Germany
Kardiologische Praxis
🇩🇪Bonn, Germany
Klinikum der Stadt Villingen Schwenningen GmbH
🇩🇪Villingen, Germany
Westfälische Wilhelms-Universität
🇩🇪Münster, Germany
Vivantes Netzwerk für Gesundheit GmbH (Humboldt)
🇩🇪Berlin, Germany
St. Johannes Hospital, Medizinische Klinik I
🇩🇪Dortmund, Germany
Georg-August-Universität, Universitätsklinikum Göttingen
🇩🇪Goettingen, Germany
Charité-Universitätsmedizin Campus Benjamin Franklin, Med. Klinik II / Kardiologie
🇩🇪Berlin, Germany