Gen 2 Battrode Wear Study

Recruiting now · Not applicable

Conditions studied: Adhesive Wear Time

In brief

Validating adhesive wear time

Key facts

Study ID

NCT07256951

Run by

Baxter Healthcare Corporation

People needed

30

Starts

2025-11-12

Expected to finish

2026-05-15

Last updated by the study team

2025-12-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Participant is ≥ 18 years.
• Completes the consent process as required.
• Participants can speak and read English fluently.
• Willing to allow shaving of device application area, as required.
• Willing to take photos of the application area before wear, daily during wear, and immediately after removal.
• Willingness to report current known pregnancy.

You may not qualify if…

• Unable to comply with the study protocol and instructions for wearing the devices for up to 15 days.
• Any pre-existing breached or compromised skin, skin rash, irritation or infection at the application area.
• Any incision, wound or scar in the application area.
• Participants with known skin allergies and sensitivities to adhesives.
• Participants with scheduled electronic imaging (including magnetic resonance imaging), cardioversion, and/or procedures where device would be removed during the data collection period.
• Participants with known history of cardiac arrhythmias.
• Participants with chest anatomies not compatible with secure parasternal placement.
• Use of clothing or garment that can dislodge or loosen the patch or bras with underwires or other worn items that might interfere with the devices under study.

Where it is running

• Orange County Research Center — Lake Forest, California, United States (enrolling)

Full record on ClinicalTrials.gov

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