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Oxitone Sp02 Hypoxia Test Versus Reference Pulse Oximetry

NCT02870179 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 11

Last updated 2017-04-20

No results posted yet for this study

Summary

The purpose of this study is to conduct a SpO2 hypoxia evaluation of the Oxitone Medical Oxitone 1000 pulse oximeter. The Oxitone 1000 pulse oximeter will be evaluated during non-motion conditions over the range of 70-100% SpO2 in comparison to a Reference Pulse Oximeter.

The study is observational in nature which quantifies device performance and accuracy in compassion to a Reference Pulse Oximeter.

Conditions

Interventions

DEVICE

Pulse Oximeter

Measurement of physiological parameters

Sponsors & Collaborators

  • Clinimark, LLC

    collaborator OTHER

  • Oxitone Medical Ltd.

    lead INDUSTRY

Principal Investigators

  • Leon Eisen, PhD · Oxitone Medical Ltd.

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-31
Primary Completion
2016-09-30
Completion
2016-09-30

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 NCT02870179 on ClinicalTrials.gov