ID.1
Item
subject is between 21 (twenty-one) and 90 (ninety) years of age at screening.
boolean
ID.2
Item
subject will have one or more of the following clinical diagnoses related to fluid-management issues: esrd, heart failure.
boolean
ID.3
Item
subject and/or legally authorized person/representative is willing to undergo the informed consent process prior to enrollment in the study.
boolean
ID.4
Item
subject is a candidate for this study based on the pi's opinion and knowledge of the subject's condition.
boolean
ID.5
Item
subject is participating in another clinical study that may affect the results of either study.
boolean
ID.6
Item
subject is unable or not willing to wear electrode patches as required.
boolean
ID.7
Item
subject has skin sensitivity to adhesive or hydrogel materials used in electrode patches.
boolean
ID.8
Item
subject has a pacemaker, implanted cardioverter-defibrillator, or ventricular assist device.
boolean
ID.9
Item
subject is considered by the pi to be medically unsuitable for study participation
boolean