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Performance Validation of a Non-contact Breathing Frequency Monitor (Model BM07)

NCT01319396 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2021-04-01

Study results available
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Summary

The purpose of this study is to compare the accuracy of the BiancaMed BM07 breathing frequency indicator device with the respiration rate measured by a SomnoScreen RC Easy device on 20+ human volunteers. This is being carried out in support of a 510(k) submission.

Conditions

  • Unspecified Threat to Breathing

Sponsors & Collaborators

  • ResMed

    lead INDUSTRY

Principal Investigators

  • Paul D Phillips, MSc, MA · ResMed

Eligibility

Min Age
10 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2010-12-31
Completion
2011-03-31

Countries

  • Ireland

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 NCT01319396 on ClinicalTrials.gov