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NCT02690298: RMI UVU

Evaluation of ExSpiron™ Measurements Derived Without Patient Specific Calibration

Completed Last updated 28 August 2018
What this trial tests

trial testing ExSpiron in Non-Invasive Respiratory Volume Monitoring in 15 participants. Completed in 30 April 2016.

Timeline
1 September 2015
Primary endpoint
30 April 2016
30 April 2016

Quick facts

Lead sponsorRespiratory Motion, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment15
Start date1 September 2015
Primary completion30 April 2016
Estimated completion30 April 2016

Drugs / interventions tested

Conditions studied

Sponsor

Respiratory Motion, Inc.

Who can join

Adults 21 to 90, any sex, with Non-Invasive Respiratory Volume Monitoring. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02690298.

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