Sticky heart patch put to the test in healthy volunteers

NCT ID NCT07158333

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

15 people

The number who actually took part.

Started

Aug 2025

Finished

Sep 2025

Lead sponsor

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

18 years and older

Sex

Anyone

Show 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

  • Orange County Research Center

    Lake Forest, California, 92630, United States

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