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Respiration Rate V2.0 in Healthy Volunteers

NCT01804062 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2015-08-10

Study results available
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Summary

The purpose of this study is to meet the respiration rate accuracy specifications for the study pulse oximeter monitoring system (study device)in a healthy volunteer population when compared to established technologies for measuring parameters related to respiration, such as Capnograph Respiration Rate (RR) (CO2).

Conditions

  • Focus of the Study is Measuring Respiratory Rate

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Scott D Kelley, MD · Medtronic - MITG

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2013-02-28
Completion
2013-02-28

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 NCT01804062 on ClinicalTrials.gov