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Prospective Study to Validate the Clinical Accuracy of the Norbert Device to Measure Pulse Rate

NCT05640323 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 37

Last updated 2023-12-20

No results posted yet for this study

Summary

The study will evaluate the mean average error (MAE) of measuring pulse rate using the Norbert Device (ND) as compared to a reference heart rate measured using an electrocardiogram (ECG).

Conditions

Interventions

DEVICE

Norbert Device

The Norbert Device (ND) is a contactless, noninvasive device that provides measurements of body temperature, oxygen saturation (SpO2), and pulse rate.

Sponsors & Collaborators

  • Northwell Health

    collaborator OTHER

  • Norbert Health

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-04-26
Primary Completion
2023-10-04
Completion
2023-10-20
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05640323 on ClinicalTrials.gov