Subjects indicated for ICD or CRT-D.
Conditions
Interventions
None listed
Sponsors
Medtronic Japan Co., Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: i, ICD or CRT-D patients who receive newly or replace to the device equipped with SST. ii, Patients who understand and sign the informed consent.
Exclusion criteria
Exclusion criteria: i, Patients who cannot visit the hospital according to the follow-up schedule or who cannot collect the data through the CareLink system. ii, Patients who are unwilling to provide written informed consent. iii, Patients who are anticipated not to be able to set the device with required programming iv, Patients who are not expected to survive more than 6 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ICD shock reduction rate with a new algorithm of Medtronic ICD/CRT-D, SST. | — |
Secondary
| Measure | Time frame |
|---|---|
| ICD shock rate and the cause of inappropriate shocks. | — |
Countries
Japan
Contacts
Public ContactRyusuke Kinoshita, Tomoyuki Yamaguchi
Medtronic Japan Co., Ltd. CRDM
Outcome results
None listed