Sticky heart patch put to the test in healthy volunteers
NCT ID NCT07158333
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested how well a heart monitor patch (MCT Patch) sticks to the skin for up to 30 days. Fifteen healthy adults wore the patch and reported on comfort and skin reactions. The goal was to see if the patch stays on long enough to record clear heart signals.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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15 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Sep 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
A total of 10 healthy evaluable subjects (wearing and returning the test article) consisting of at least 5 males and 5 females is the desired sample size.
- Ages
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18 years and older
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Each subject must meet the following criteria to be enrolled in this study: 1. Subject is ≥18 years of age. 2. Completes the consent process as required. 3. Subject can speak and read English fluently. 4. Subject is willing to allow shaving of device application area, as required. 5. Subject is willing and able to take photos of the application area before, during, and immediately after wear of each Adhesive Patch Exclusion Criteria: 1. Unable to comply with the study protocol and instructions for wearing the MCT Patch for up to 30 days. 2. Geographically located such that they cannot have the initial MCT Patch placed by PI or designee. 3. Any breached or compromised skin, skin rash, irritation or infection over the sternum (prior to the initial application) as reported by the subject and/or observed by the PI during initial application. 4. Had any sternal incision or wound within 3 months prior to the date of enrolment. 5. Subjects with sensitive skin or known skin conditions, including known allergies. 6. Subjects with scheduled cardioversion during the data collection period. 7. Subjects with a scheduled electronic imaging (including magnetic resonance imaging) during the data collection period. 8. Subject has known cardiac arrhythmia conditions (Note: The PI will assess the subject during initial screening. If an arrhythmia is discovered during the subject will be deemed ineligible for participation in the study).
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Orange County Research Center
Lake Forest, California, 92630, United States
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