Bradycardia Clinical Trial
Official title:
INGENIO MRI/ FINELINE II ImageReadyTM Pacing System Data Collection in Patients Undergoing Magnetic Resonance Imaging
The INFINITE MRI Study is a prospective, non-randomized, multicenter, single arm study aimed at collecting data on ImageReady™ MR Conditional Pacing System (consisting of an INGENIO™ MRI or ADVANTIO™ MRI pacemaker with FINELINE™ II Sterox or FINELINE™ II Sterox EZ endocardial pacing lead(s)) when used in the Magnetic Resonance Imaging environment under the labeled Conditions of Use.
Objective of the INFINITE MRI Study is to collect data on the ImageReady MR Conditional
Pacing System in subjects undergoing a magnetic resonance scan (MRI).
The ImageReady system has CE mark and enrolled patients will undergo MRI scan under the
labeled Conditions of Use. Subjects considered eligible for this studty are already
implanted with the system according to standard medical guidelines for PM implantation.
The study is aimed at providing confirmatory data of no impact of MRI on device function,
lead parameters and patient conditions. The study will collect standard device measurement
through device interrogation pre- and post- MRI scan. MRI scan in this study is a
non-clinically indicated procedure and is not planned for diagnostic purposes.
Data from this study will be used to support the evidence of clinical performance of the
ImageReady™ MR Conditional Pacing System following a MRI scan when used under the labeled
Conditions of Use, and may be used to support regulatory submissions for the approval of the
system where requested.
The study has no primary endpoint and is not hypothesis driven.
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