MedTrace Logo

Evaluation of ExSpiron™ Measurements Derived Without Patient Specific Calibration

NCT02690298 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2018-08-28

No results posted yet for this study

Summary

Previous studies have shown that the ExSpiron™ can provide non-invasive, real-time, accurate measurements of minute ventilation (MV), tidal volume (TV) and respiratory rate (RR) after calibration with a spirometer. The purpose of this study is to compare the MV, TV and RR values measured by the ExSpiron™ without prior spirometer calibration to values obtained with a spirometer calibration. In this study, the MV and TV values will be compared between the ExSpiron™ with and without prior patient-specific calibration of the ExSpiron™ to a spirometer

Conditions

  • Non-Invasive Respiratory Volume Monitoring

Interventions

DEVICE

ExSpiron

Non-Invasive respiratory volume monitoring

Sponsors & Collaborators

  • Respiratory Motion, Inc.

    lead INDUSTRY

Eligibility

Min Age
21 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-09-01
Primary Completion
2016-04-30
Completion
2016-04-30

More Related Trials

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 NCT02690298 on ClinicalTrials.gov