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RECRUITINGOBSERVATIONAL

Evaluation of the SCALED (SCaling AcceptabLE cDs)

Evaluation of the SCALED (SCaling AcceptabLE cDs) Approach for the Implementation of Interoperable CDS for Venous Thromboembolism Prevention - CDS Data

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This project will adapt a currently deployed Clinical Decision Support (CDS) system to deliver a VTE prevention guideline for adult patients with traumatic brain injury (TBI). We believe this is an ideal PCOR use case given PCORI's continued effort to combat VTE in trauma and our experience previously implementing this guideline. The Our overall goal is to successfully scale, evaluate, and maintain an interoperable TBI CDS across 7 total institutions.

Who May Be Eligible (Plain English)

Who May Qualify: - age 18 and older - admitted with a TBI Who Should NOT Join This Trial: - Patients who die within 24 hours of hospital admission and patients documented as "comfort cares" during the first 72 hours of hospitalization or with mild TBI will be excluded from final analysis. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * age 18 and older * admitted with a TBI Exclusion Criteria: * Patients who die within 24 hours of hospital admission and patients documented as "comfort cares" during the first 72 hours of hospitalization or with mild TBI will be excluded from final analysis.

Treatments Being Tested

OTHER

Observational

There is no intervention, the hospitals will adopt a CDS system which prompts users to follow best practice guidelines.

OTHER

Observational-control

There is no intervention, the hospitals will not use the CDS system.

Locations (1)

University of Minnesota
Minneapolis, Minnesota, United States