MedPath

FEAT-AT

Not Applicable
Conditions
Subjects indicated for pacemaker, ICD, or CRT.
Registration Number
JPRN-UMIN000008593
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
553
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients who cannot be set the device with the required A-ATP programming. 2) Patients with permanent Af. 3) Patients who cannot visit the hospital according to the follow-up schedule or who cannot collect the data through the CareLink system. 4) Patients who are unwilling to provide written informed consent. 5) Patients who are not anticipated to complete this study. 6) Patients who are limited to participate this study due to his/her medical condition.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A-ATP success rate on AT.
Secondary Outcome Measures
NameTimeMethod
1) Prevalence of AT 2) Acceleration rate by A-ATP 3) Comparison of the prevalence of AT between patients with or without a history of AT. 4) Prevalence of AT in patients with pacemaker, ICD, or CRT.
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