Dysfunctional Hemoglobin Pulse Oximetry

NCT03030833 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2017-09-01

No results posted yet for this study

Summary

The purpose of the study is to assess device performance in the presence of carbon monoxide.

Conditions

  • Carbon Monoxide Poisoning

Interventions

DEVICE

Pulse Oximeter

Comparison of pulse oximetry to blood gas analyzer.

Sponsors & Collaborators

  • Nonin Medical, Inc

    lead INDUSTRY

Principal Investigators

  • David B MacLeod, MD · Duke University

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-06
Primary Completion
2017-04-30
Completion
2017-04-30
FDA Device
Yes

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 NCT03030833 on ClinicalTrials.gov