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Clinical Trial Summary

This study will obtain device-human interaction evaluations for the HWD1000 within the controlled environment of the hospital as well as establish that the safety profile is similar to outpatient wearable cardioverter-defibrillators use.


Clinical Trial Description

A multi-center prospective study of hospitalized patients whom a physician deems at risk of sudden cardiac arrest during the hospitalization period, wearing the HWD1000 hospital wearable defibrillator in order to evaluate caregiver and patient interactions with the device. In addition, ECG signal quality will be reviewed to confirm the HWD1000 safety profile. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02122549
Study type Interventional
Source Zoll Medical Corporation
Contact
Status Completed
Phase N/A
Start date April 2014
Completion date July 2015

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