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Surveillance Monitoring on General Wards

Surveillance Monitoring on General Wards

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03271216
Enrollment
422
Registered
2017-09-05
Start date
2014-02-28
Completion date
2015-02-28
Last updated
2017-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest

Brief summary

This is a study to determine if surveillance monitoring of general ward patients can reduce cardio-pulmonary arrest while maintaining an acceptable false alarms rate for nursing workload.

Detailed description

The investigators placed a wired monitoring system (pulse oximetry, heart rate and respiratory rate) on every patient who arrived on a subject general post surgical ward who assented to wear the system. this was the Masimo PSNET system using the Radical 87 monitor and an acoustic respiratory sensor along with a Masimo pulse oximetry probe. Patients were monitored for a minimum of 48 hrs. Heart Rate (HR) parameters were set between 45-130, Respiratory rate was set between 6-20 and pulse oximetrry was 85-100%. Nurses documented in the Electronic Medical Record (EMR) any alarms they responded to as to whether they were false (vital sign not out of range when rechecked) or true and what the response was. Responses ranged from nurse managed to notification of primary service to Rapid Response Activation to Code team activation as well as transfer to a higher level of care (operating room or Intensive Care Unit (ICU)/IMC. Patient and Nursing satisfaction surveys were collected.

Interventions

DEVICENo intervention

no intervention

Sponsors

Masimo Corporation
CollaboratorINDUSTRY
Johns Hopkins University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* all post-surgical patients admitted to a post-operative general hospital ward

Exclusion criteria

* inability to understand English or provide verbal consent for data analysis

Design outcomes

Primary

MeasureTime frameDescription
positive predictive value (PPV)6 monthsThe PPV of the wired monitoring system (pulse oximetry, heart rate and respiratory rate) will be determined based on change in vital signs (HR\<45 or \>130, RR\<6 or \>20 and pulse oximetry \<85) indicating clinical deterioration

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026