Use of AliveCor ECG Monitoring to Replicate ECG Lead Recording

Mayo Clinic

Status: Withdrawn

Conditions: Arrhythmia

Treatments: Device: AliveCor Heart Monitor

Study type: Interventional

Funder types: Other

Identifiers

NCT04472520

18-002678

Details and patient eligibility

About

The researchers are trying to determine whether the Alivecor device can simulate other electrocardiogram (ECG) leads to record electrical activity.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Individuals greater than 18 years old getting an ECG

Exclusion criteria

• Patients unwilling or unable to provide informed consent

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

Subject getting an ECG

Experimental group

Description:

Subjects getting an ECG will have AliveCore tracings obtained in 3 configurations; between right hand and left hand, between left hand and left lower leg (thigh, calf, and foot) and between right hand and left lower leg (thigh, calf, and foot).These configurations will be obtained with the participant lying in bed and in a sitting position.

Treatment:

Device: AliveCor Heart Monitor