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Point-Of-Care Ultrasound-Driven vs Standard Diagnostic Pathway in Emergency Department Patients With Dyspnea

Effect of a Point-Of-Care Ultrasound-Driven vs Standard Diagnostic Pathway on 24-Hour Hospital Stay in Emergency Department Patients With Dyspnea - a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05674916
Acronym
POCUS PATHWAY
Enrollment
674
Registered
2023-01-09
Start date
2023-01-25
Completion date
2024-09-25
Last updated
2024-10-01

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

Conditions

Dyspnea

Keywords

Point-of-care Ultrasound, Emergency Medicine, Diagnostic pathways

Brief summary

The POCUS PATHWAY-trial is a multi-center, randomized, investigator-initiated, open labelled, pragmatic, controlled trial of a point-of-care ultrasound-driven diagnostic pathway vs standard diagnostic pathway in dyspneic emergency department patients. The primary outcome will be 24-hour hospital stay and 642 patients will be included. Key secondary outcomes include overall hospital length of stay, image resources, and 72-hour revisits.

Interventions

DIAGNOSTIC_TESTPoint-of-care ultrasound-driven diagnostic pathway

Focused lung ultrasound will include 8 zones (anterior and lateral) and evaluate pneumothorax, interstitial syndrome, lung consolidation, and pleural effusion. Focused cardiac ultrasound will include four views (subxiphoid four-chamber view, parasternal long-axis view, parasternal short-axis view, and apical four-chamber view) and evaluate pericardial fluid, right ventricle dilation, and left ventricular systolic contractility.

Sponsors

Aarhus University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

1. Emergency department contact 2. Age ≥ 18 years 3. Chief complaint is Dyspnea 4. Including physician present

Exclusion criteria

1. Fulfilling of criteria for coded rapid-response teams (i.e., trauma, surgical or medical emergencies). 2. Prior focused lung or focused cardiac ultrasound in the current emergency department stay 3. Prior enrollment in the trial 4. Unable to consent 5. Non Danish-speaking

Design outcomes

Primary

MeasureTime frameDescription
24-hour hospital stayFrom date of hospital admission until the date of first documented hospital discharge, assessed up to 24 hours.Proportion of patients with a hospital lenght-of-stay of less than 24 hours.

Secondary

MeasureTime frameDescription
Hospital length-of-stayFrom date of hospital admission until the date of first documented hospital discharge, assessed up to 3 months.Hospital length-of-stay will secondarily be analyzed using time-to-event analysis.
Image resourcesFrom date of hospital admission until the date of first documented hospital discharge, assessed up to 3 months.Image resources will be presented as a composite absolute number and incidence proportion counting the cumulative number of participants having received any of the following imaging techniques during the current hospital stay: chest x-rays, echocardiography, computed tomography (CT) angiography, and CT thorax.
Number of participants with the composite outcome of 72-hour revisits and overall mortalityFrom date of hospital admission until 72 hours after the date of first documented hospital discharge, assessed up to 3 months.72-hour revisits will be defined as a composite outcome including any unplanned hospital stay within 72 hours from the previous hospital discharge, in-hospital mortality, and mortality within 72 hours from the previous hospital discharge.

Countries

Denmark

Outcome results

None listed

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