A Usability Study of a Multi-channel ECG Monitoring Device
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWearlinq
About this trial
This study it to evaluate the usability of the WearLinq eWave patch in a general adult population.
Eligibility criteria
Qualifiers
Adult >18 years old and able to consent
Capable of using a smartphone app
Willing to shave patch area if needed
Disqualifiers
Planning to undergo an MRI during the study period
Known allergic reaction to adhesives or hydrogels or with family history of adhesive skin allergies, or any other dermatological conditional that could confound placement or results
Presence of pacemaker, ICD or other implanted electronic devices
Open wounds, lesions or infected or inflamed areas of skin at the placement site (left-center of chest/sternum)
Trial design
Treatments tested in this trial
- eWave Patch
Treatment groups
500 Participants
are divided into 2 treatment groupsLocations
1ABio Clinical Research Partners28127, New LondonNorth Carolina, United States
Sponsors and collaborators
Wearlinq
Lead sponsor
ABio Clinical Research Partners
Collaborator
Source ClinicalTrials.gov