Everbeat Ring ECG Clinical Concordance Study

Grektek

Status: Not yet enrolling

Conditions: Cardiovascular Diseases

Treatments: Device: Everbeat Ring

Study type: Observational

Funder types: Industry

Identifiers

NCT05469542

Pro00064656

Details and patient eligibility

About

This study is a cross-sectional observational study conducted in patients referred for routine ECG, to compare output from the everbeat finger-worn ECG device to standard of care (SOC) 12-lead electrocardiography. No intervention is involved in this study. Patients visiting the study site during the study period will be assessed for eligibility on a convenience basis, and observational data will be recorded on those eligible.

Enrollment: 65 estimated patients

Sex: All

Ages: 18 to 90 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Males or females aged 18 to 90 years.
• Under the care of a board-certified physician and referred for a routine electrocardiogram (ECG)
• Resting heart rate between 50 to 120 beats per minute (BPM).

Exclusion criteria

• Inability to wear the everbeat ring.
• Prior history of movement disorders including Parkinson's or benign tremors.
• Prior history of allergic skin reactions to metal including stainless steel.