CompletedNot Applicable

Improved Patient Safety Through Continuous Bi-channel RR and SpO2 Monitoring With Masimo Patient SafetyNet

United States87 participantsStarted 2017-09-19

Plain-language summary

The investigator intend to perform an observational study, by adding Respiratory Rate monitoring to an already existing Patient SafetyNet system with SpO2 (Oxygen Saturation) and PR (Pulse Rate) monitoring. RRa will be blinded to the clinicians and all RRa alarms will be deactivated. Retrospective analysis of the observational data collected will be utilized to evaluate the potential benefits of additional continuous respiratory rate monitoring.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * • Adult 18yrs of age or older * Post-surgical patient receiving opioid pain medication Exclusion Criteria: * • Refusal of optical finger sensor and/or acoustic respiratory rate neck sensor placement * Finger or skin abnormalities at sensor sites * Expected opioid therapy duration less than 24 hours

What they're measuring

Improved sensitivity of RRa by detecting the number and the incidence rate of respiratory depression events

Timeframe: with in 24 hours post surgery

Trial details

NCT IDNCT03043911

SponsorBaylor Research Institute

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2021-11-10

View on ClinicalTrials.gov More Signs and Symptoms, Respiratory trials