The purpose of the study is to proof the safety and efficacy of the new ICD sytem (Iforia/Ilesto). The devices are available with DF-1 and DF4 connection. A special focus is set on the ICD system with DF4 connection.
Study Type
OBSERVATIONAL
Enrollment
240
Universitaetsmedizin Greifswald
Greifswald, Germany
Serious adverse device effect (SADE) rate related to the ICD with DF4 connection
Time frame: until 3 month follow-up
SADE rate related to the Linox smart DF4 lead (ICD shock lead)
Time frame: until 3 month follow-up
Shift rate of the painless shock impedance measurement
Time frame: between 3 and 6 month follow-up
Pacing threshold comparison between Linox smart DF-1 and Linox smart DF4 lead
Time frame: 3 month follow-up
Comparison of automatic atrial pacing threshold test vs. manual measurement
Time frame: 3 month follow-up
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