Arrhythmia Management System (AMS)
DeviceAMS records rhythm, heart rate, subject-reported symptoms, and multiple parameters that include respiration rate, activity and body posture.
NCT Number: NCT04754204
To determine the associations among biometric data, arrhythmias, subject-reported symptoms and subject wellness.
Looking for future studies?
Notify Me21 year and older
All sexes
Observational
Comprehensive Cardiovascular Medical Group, Bakersfield, California, United States
The Arrhythmia Management System records rhythm, heart rate, subject-reported symptoms and multiple parameters that include respiration rate, activity and body posture. These biometric data could provide clinicians better insight into the context of the detected arrhythmias, subject-reported symptoms and wellness status. Hence, the purpose of the study to determine the associations among biometric data, arrhythmias, symptoms and subject wellness.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
AMS records rhythm, heart rate, subject-reported symptoms, and multiple parameters that include respiration rate, activity and body posture.
Time frame: 30 days
MCT Data Sets
Time frame: 30 days
MCT Data Sets
Time frame: 30 days
MCT Data Sets
Time frame: 30 days
Clinical Case Report Forms
Time frame: 30 days
Clinical Case Report Forms
Time frame: 30 days
Clinical Case Report Forms
Looking for future studies?
Notify MeZoll Medical Corporation
Industry
Mobile Cardiac Telemetry and Advanced Multi-Parameter Monitoring in Patients Wearing a Novel Device
Acronym: MAPS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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