Evaluation of Defibrillation SAfety with the Increased Number of Sensing to Reduce ShocKS for Ventricular Tachyarrhythmia in Japanese ICD Patients
Not Applicable
- Conditions
- ICD or CRT-D cases
- Registration Number
- JPRN-UMIN000003442
- 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
- 186
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients whoes clinical condition are not acceptable to VF induction tests. 2) Patients who are limited to participate this study due to their clinical condition. 3) Patients who can not sign the informed consents.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method a, VF termination rate by ICD shock therapy in VF induction test. b, Inappropriate shock reduction rate by simutating NID as 30/40.
- Secondary Outcome Measures
Name Time Method Time from VF induction and detection to VF termination.