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Effectiveness of Point of Care Complete Blood Cell Count Analyzer in Reducing Time to Results

Effectiveness of Point of Care Complete Blood Cell Count Analyzer in Reducing Time to Results

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04769336
Enrollment
100
Registered
2021-02-24
Start date
2021-04-01
Completion date
2022-03-31
Last updated
2021-02-24

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

Conditions

Laboratory Problem

Brief summary

The current process for getting complete blood cell counts (CBC) results in the operating room during surgery relies on sending blood samples from the operating room to the hospital's central lab. This workflow is complex and often results in handing off the blood sample to 4 or more different staff members before arriving in the lab for analysis. This often causes delayed CBC results, which may lead to inappropriate or delayed clinical decision making. By providing prompt access to CBC results with the use of a point of care CBC analyzer, the clinical workflow efficiency can be significantly improved. This should resulting in better clinical decision making, reductions in costs, increase in patient satisfaction and facilitation of hospital processes.

Interventions

DEVICECentral Lab based CBC

lab samples will be sent to the central lab for CBC analysis

DEVICEPoint of Care CBC

lab samples will be analyzed at point of care

Sponsors

Northwestern Medicine
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* All English speaking patients, 18 years or older, having surgery in the Lake Forest Hospital operating rooms, with a pre-existing indication for CBC analysis.

Exclusion criteria

* All patients not meeting inclusion criteria or protected patient populations, specifically, pregnant women, prisoners, cognitively impaired patients, patients unable to consent, students, employees, and children)

Design outcomes

Primary

MeasureTime frameDescription
Time to resultThrough study completion, an average of 1 yearTime between blood draw and CBC result displayed in Electronic medical record

Countries

United States

Outcome results

None listed

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