Necklace-Shaped Sensor for Non-Invasive Remote Monitoring of Vitals

Completed

Conditions studied: Heart Failure, Hypertension

In brief

This study is designed to validate the use of the CoVa Monitoring System in subjects with implanted devices.

Key facts

Study ID

NCT02337790

Run by

Baxter Healthcare Corporation

People needed

109

Starts

2015-01-01

Expected to finish

2015-05-01

Last updated by the study team

2015-12-30

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is between 21 (twenty-one) and 95 (ninety-five) years of age at screening.
• Subject has a pacemaker, implanted cardioverter-defibrillator, or ventricular assist device.
• 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 is considered by the PI to be medically unsuitable for study participation.

Where it is running

• Imperial Cardiac Center — Imperial, California, United States

Full record on ClinicalTrials.gov

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