Everbeat Ring ECG Clinical Concordance Study

Status unconfirmed

Conditions studied: Cardiovascular Diseases

In brief

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.

Key facts

Study ID

NCT05469542

Run by

Grektek Inc.

People needed

65

Starts

2022-08-01

Expected to finish

2022-09-20

Last updated by the study team

2022-07-21

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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).

You may not qualify if…

• 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.

Where it is running

• BKLYNCardio — Brooklyn, New York, United States

Full record on ClinicalTrials.gov

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