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ST Monitoring to Detect Acute Coronary Syndrome Events in Implantable Cardioverter Defibrillator Patients (AnalyzeST)

Patient Information

This is a prospective, non-randomized, multicenter, pivotal Investigational Device Exemption (IDE) study. The intent of this study is to demonstrate the safety and effectiveness of the ST Monitoring Feature in the Fortify® ST ICD system (or other Implantable Cardioverter Defibrillator (ICD) systems with the ST Monitoring Feature).

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Clinical Trial Categories

  • Electrophysiology Trials

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