The Validation Study of Bioelectronics
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorUniversity of North Carolina, Chapel Hill
About this trial
The purpose of this study is to investigate the safe wearability and basic functions of the multi-modality sensors fabricated in the PI lab.
Eligibility criteria
Qualifiers
Individuals with ages between 18 and 99.
Healthy individuals (not known to suffer any significant illness relevant to the proposed study).
Disqualifiers
Pregnant or lactating.
History of active (clinically significant) skin disorders that make skin vulnerable to contact conventional electronic devices.
History of allergic response to silicones or adhesives (such as 3M Tegaderm).
Broken, damaged or irritated skin or rashes near the sensor application sites (finger, wrist, temple, subclavian, arm, neck, and thigh).
Trial design
Treatments tested in this trial
- Multi-modality Noninvasive Biosensor
- Oximeter
- Portable Blood Pressure Monitor
- Vicorder Pulse Wave Velocity Monitor
Treatment groups
22 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of North Carolina, Chapel Hill
Lead sponsor
North Carolina Translational and Clinical Sciences Institute
Collaborator
Source ClinicalTrials.gov