MedPath

DEFENSE Trial

Not Applicable
Conditions
Subjects indicated for ICD or CRT-D.
Registration Number
JPRN-UMIN000007212
Lead Sponsor
Medtronic Japan Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
151
Inclusion Criteria

Not provided

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.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ICD shock reduction rate with a new algorithm of Medtronic ICD/CRT-D, SST.
Secondary Outcome Measures
NameTimeMethod
ICD shock rate and the cause of inappropriate shocks.
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