Reassure Device: Measurement Accuracy of Continuous Respiration Rate

NCT02740478 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2021-04-02

Study results available
· View outcomes & findings →

Summary

The aim of the trial is to prove that the Reassure10.5 GHz sensor is equivalent in performance to the SomnoScreen Plus RC in indicating the breathing rate of adult subjects over a number of hours when the subjects are lying still or in bed asleep

Conditions

  • Accuracy of Respiration Rate Measurement

Sponsors & Collaborators

  • ResMed

    lead INDUSTRY

Principal Investigators

  • Paul Phillips, MA, MSc · ResMed Sensor Technologies Ltd

Eligibility

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

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2015-07-31
Completion
2015-07-31

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 NCT02740478 on ClinicalTrials.gov