Actively Recruiting
Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07256951
Gen 2 Battrode Wear Study
Led by Baxter Healthcare Corporation · Updated on 2025-12-01
30
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Validating adhesive wear time
CONDITIONS
Official Title
Gen 2 Battrode Wear Study
Who Can Participate
Age: 18Years +
All Genders
Healthy Volunteers
Eligibility Criteria
You may qualify if you...
- Participant is 18 years or older
- Completes the consent process as required
- Can speak and read English fluently
- Willing to allow shaving of the device application area if needed
- Willing to take photos of the application area before wear, daily during wear, and immediately after removal
- Willing to report current known pregnancy
You will not qualify if you...
- Unable to comply with the study protocol and instructions for wearing the device for up to 15 days
- Any pre-existing breached or compromised skin, rash, irritation, or infection at the application area
- Any incision, wound, or scar in the application area
- Known skin allergies or sensitivities to adhesives
- Scheduled electronic imaging, cardioversion, or procedures requiring device removal during data collection
- Known history of cardiac arrhythmias
- Chest anatomy incompatible with secure parasternal placement
- Use of clothing or garments that could dislodge or loosen the patch, including bras with underwires or other interfering items
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Trial Site Locations
Total: 1 location
1
Orange County Research Center
Lake Forest, California, United States, 92630
Actively Recruiting
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How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DEVICE_FEASIBILITY
Number of Arms
2
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