Electrocardiogram (ECG): The intervention consists of non-invasive ECG recordings obtained using the HeartBeam System. Participants will use the device to capture cardiac electrical activity for assessment of heart rhythm, conduction patterns, and heart rate abnormalities in a clinical setting.
Study summary
The HeartBeam ECG Registry will collect ECG recordings acquired with the HeartBeam System with relevant clinical information in clinical settings.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
1. Undergoing ECG as part of standard of care.
2. Able and willing to provide written informed consent.
Exclusion Criteria:
1. Open chest wounds or surgery to the chest or abdomen within 30 days.
2. Inability to complete ECG acquisition with either HeartBeam device or standard 12-L ECG.
3. Unstable condition where registry participation may interfere with care.
Primary outcome measure(s)
Creation of a de-identified ECG dataset for future research and regulatory use — 2 years ECG recordings collected during the study will be de-identified and compiled into a database that may be used by HeartBeam for future research and regulatory submissions. The collected data are for observational purposes only and will not be used for clinical decision-making.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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