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Predicting Outcomes for Covid-19 Using Sonography

Predicting Outcomes for Covid-19 Using Sonography

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04384055
Acronym
POCUS
Enrollment
165
Registered
2020-05-12
Start date
2020-03-21
Completion date
2021-11-15
Last updated
2021-12-03

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

Conditions

COVID-19, Pneumonia, Viral

Brief summary

This study seeks to investigate the role of lung ultrasound in caring for Covid-19 positive patients and whether it can be used to predict patient deterioration. This information will be vital for healthcare workers who seek to identify Covid-19 pneumonia or patients at risk for deterioration early in the disease course.

Detailed description

As Covid-19 continues to stress hospital-based resources (including personal protective equipment, ancillary staff availability, and imaging study utilization), it is important to assess whether alternative methods for evaluating patients can be utilized to appropriately triage and care for Covid-positive patients. Current limitations of caring for patients with Covid-19 include the exposure of ancillary healthcare workers (including radiological technicians) and the time/resources required to decontaminate traditional radiological equipment such as x-ray or computerized tomography (CT) machines. Point-of-care ultrasound (POCUS) has the potential to transform healthcare delivery due to its diagnostic and therapeutic expediency. It can be quickly performed at the bedside by experienced clinicians. It it has been shown to reliably and accurately diagnose patients with a variety of lung diseases, including pneumonia. This study seeks to investigate the role of lung ultrasound in caring for Covid-19 positive patients and whether it can be used to predict patient deterioration. This information will be vital for healthcare workers who seek to identify the virus or patients at risk for deterioration early in the disease course. Moreover, it has the potential to reduce the need for x-rays or CTs for Covid-19 patients, which has the potential to alleviate a significant burden currently being placed on the healthcare system.

Interventions

DIAGNOSTIC_TESTLung Ultrasound

Lung ultrasound will be performed on patients undergoing investigation for covid-19 based on a nasopharyngeal PCR.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Any adult (18 or more years of age) presenting to the emergency department with symptoms suspicious for Covid-19 * This individual underwent evaluation for Covid-19 via a nasopharyngeal RT-PCR * This individual received a lung ultrasound by the study authors within 28 days from initial evaluation

Exclusion criteria

* Any individual who did not receive a lung ultrasound within 28 days from initial evaluation for covid-19 related illness

Design outcomes

Primary

MeasureTime frameDescription
Number of Patients Experiencing Death, ICU Admission, Mechanical Ventilation, or Use of High-Flow Nasal Cannula28 days from initial evaluationComposite primary outcome of death, ICU admission, mechanical ventilation, or use of high-flow nasal cannula (categorical)

Secondary

MeasureTime frameDescription
Number of Patients Requiring Mechanical Ventilation28 days from initial evaluation
Number of Patients Requiring Supplemental Oxygen Usage28 days from initial evaluation
Duration of Supplemental Oxygen Usage28 days from initial evaluation
Length of Stay28 days from initial evaluationDuration of Hospitalization (days)
Characterization of Ultrasound Findings28 days from initial evaluationDescriptive analysis of ultrasound findings in Covid-19

Countries

United States

Outcome results

None listed

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