Monitoring Subjects With Fluid-Management Issues In the Home Environment

Completed

Conditions studied: Heart Failure, Hypertension

In brief

This study is designed to validate ease-of-use for the CoVa Monitoring System, along with simple statistical parameters such as reproducibility and inter-subject agreement between test and reference devices.

Key facts

Study ID

NCT02190877

Run by

Baxter Healthcare Corporation

People needed

23

Starts

2014-04-01

Expected to finish

2014-05-01

Last updated by the study team

2014-07-23

Who can join

Age: 21 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is between 21 (twenty-one) and 90 (ninety) years of age at screening.
• Subject will have a current prescription for a diuretic medication.
• Subject and/or legally authorized person/representative is willing to undergo the Informed Consent process prior to enrollment in the study.
• Subject is a candidate for this study based on the PI's opinion and knowledge of the subject's condition.

You may not qualify if…

• Subject is participating in another clinical study that may affect the results of either study.
• Subject is unable or not willing to wear electrode patches as required.
• Subject has skin sensitivity to adhesive or hydrogel materials used in electrode patches.
• Subject has a pacemaker, implanted cardioverter-defibrillator, or ventricular assist device.
• Subject is considered by the PI to be medically unsuitable for study participation.

Where it is running

• Riverside Meadows — Riverside, California, United States

Full record on ClinicalTrials.gov

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