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Respiration Rate Monitoring During Transitions

NCT01881269 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 27

Last updated 2013-11-06

No results posted yet for this study

Summary

The purpose of this study is to evaluate the performance of the software that calculates respiration rate for the study pulse oximetry monitoring system during transitions of ventilation type from spontaneous breathing to controlled ventilation.

Conditions

  • Focus of the Study is Measuring Respiratory Rate

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Joshua Lumbley, MD · Ohio State University

Eligibility

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

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2013-07-31
Completion
2013-09-30

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 NCT01881269 on ClinicalTrials.gov