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Binah.ai Visual Vitals Application - Validation Study

NCT05539612 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2022-10-13

No results posted yet for this study

Summary

The purpose of this study is to conduct a Respiratory and Pulse Rate accuracy validation comparing the Binah.ai Visual Vitals Application to the Reference, an FDA cleared End Tidal Carbon Dioxide monitor (GE Datex-Ohmeda), and a standard ECG reference (respectively).

Conditions

  • Respiratory and Pulse Rate Accuracy Validation

Sponsors & Collaborators

  • Clinimark, LLC

    collaborator OTHER

  • Binah.ai LTD.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-18
Primary Completion
2022-08-12
Completion
2022-08-12

Countries

  • United States

Study Locations

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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 NCT05539612 on ClinicalTrials.gov