Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Baxter Healthcare Corporation
The study had the following objectives:
1. Verify that the CoVa Monitoring System does not interfere with implanted devices.
2. Verify that implanted devices do not interfere with the functions of the CoVa Monitoring System.
3. Verify that the CoVa Monitoring System fits on a wide variety of body types.
Age
18–90
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible 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 be 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.
Clareo Health | Necklace-Shaped Sensor for Non-Invasive Remote Monitoring of Vitals
