Investigation of the efficacy and safety of the Ventricular Pace Suppression (VpS) algorithm.
Device: VpS algorithm in EVIA and ENTOVIS pacemakers
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Full eligibility criteria for NCT01053832
Ages eligible for Study
Genders eligible for Study
Accepts Healthy Volunteers
Paroxysmal AV block and/or Sinus Node Dysfunction
DDD(R)-ADI(R)-Mode (VpS Algorithm) applicability
Permanent AV block III°
Permanent Atrial Fibrillation/ Flutter
Require mode other than DDD(R)-ADI(R) or DDD(R)
Have a life expectancy of less than six months
Expected to receive heart surgery within six months
Enrolled in another cardiac investigation
All locations for NCT01053832
Klinikum Coburg gGmbH
Coburg, Bavaria, Germany, 96450
Abteilung für Elektrophysiologie, Klinik für Kardiologie und Angiologie, UNIVERSITÄTSKLINIKUM Schleswig-Holstein
Kiel, Schleswig-Holstein, Germany, 24105
View full eligibility
Tris trial is registered with FDA with number: NCT01053832. The sponsor of the trial is Biotronik SE & Co. KG and it is looking for 84 volunteers for the current phase.
Official trial title: Ventricular Pace Suppression Study With the EVIA/ENTOVIS DR-T/DR Pacemaker
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