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N/A N=21

Reassure Device: Measurement Accuracy of Continuous Respiration Rate

Accuracy of Respiration Rate Measurement

Enrolled (actual)
21
Serious AEs
0.0%
Results posted
Apr 2021
Primary outcome: Primary: Respiration Rate Comparability — 0.4 breaths per minute

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
ResMed
Primary completion
Jul 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Respiration Rate Comparability
0.4

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

Eligibility Criteria

Inclusion Criteria

  • Willing Volunteer

Exclusion Criteria

  • Restless leg syndrome
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02740478). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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