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NCT04472520 Clinical Trial

Use of AliveCor ECG Monitoring to Replicate ECG Lead Recording

Arrhythmia Clinical Trial

Official title:
Use of AliveCor ECG Monitoring to Replicate ECG Lead Recording

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04472520
Other study ID # 18-002678
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 1, 2021
Est. completion date December 31, 2022

Study information
Verified date July 2020
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date December 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Individuals greater than 18 years old getting an ECG

Exclusion Criteria:

- Patients unwilling or unable to provide informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• AliveCor Heart Monitor
Records single-channel ECG rhythms

Locations
Country Name City State
United States Mayo Clinic Arizona Phoenix Arizona

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Electrocardiogram (ECG) QT Interval The QT interval represents the time of ventricular activity including both depolarization and repolarization. It is measured from the beginning of the QRS complex to the end of the T wave. Normally, the QT interval is 0.36 to 0.44 seconds 1 day
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