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This study is designed to be a clinical validation study to ready the CPM System for FDA 510(k) submission. This study will be conducted as a prospective non-randomized. The study is non-significant r...
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Lead Sponsor
Analog Device, Inc.
Collaborators
NCT03999138 · Acute Heart Failure, Pulmonary Edema With Heart Failure
NCT03103932 · Heart Failure; With Decompensation
NCT06762964 · Fontan Circulation, Single Ventricle Heart Disease, and more
NCT04347655 · Heart Failure
NCT06307652 · Heart Failure and Impaired Kidney Function
Mayo Clinic Hospital
Rochester, Minnesota
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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