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A Study to Evaluate Rapid Throughput Screening for Human COVID-19 Infection

Rapid Throughput Screening for Human COVID-19 Infection: A ECG Study

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04725097
Enrollment
2821
Registered
2021-01-26
Start date
2020-12-10
Completion date
2021-06-03
Last updated
2021-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19

Brief summary

The purpose of this study is to assess the ability of an artificial intelligence smartphone-enabled point of care ECG to detect COVID-19.

Interventions

None listed

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Adult males and females age 18 or greater. * Undergoing COVID-19 testing by PCR. * Willing and able to provide informed consent. * Pregnant females (minimal risk study, no risk from ECG).

Exclusion criteria

\- Unwilling or unable to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
COVID 19 DetectionOne time screening within 4 hours of PCR testDetermine the safety and feasibility of the POC AI-ECG's ability to detect active SARS-Cov-2 infection in humans.

Countries

India, Spain, United Kingdom, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026