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Clinical Trials/NCT04368338
NCT04368338
Completed
Not Applicable

Use of Lung Ultrasound in Patients Suspected of COVID-19 Infection in the Emergency Room

Centre Hospitalier Universitaire, Amiens1 site in 1 country100 target enrollmentApril 28, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid-19
Sponsor
Centre Hospitalier Universitaire, Amiens
Enrollment
100
Locations
1
Primary Endpoint
Lung ultrasound/biological correlation research modulating the severity of Covid-19 disease
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Covid-19 (English acronym meaning coronavirus disease 2019) is an emerging infectious disease caused by a strain of coronavirus called SARS-CoV-2. The current pandemic has resulted in a significant number of admissions in the emergency room (ER) due to suspicion of COVID-19 infection. Use of lung ultrasound is standard practice to diagnose acute respiratory failure in ER. Recently, typical lung ultrasonographic characteristics of COVID-19 disease has been described. During the COVID-19 pandemic, the use of this tool could be of interest in order to allow an early, simple and reliable triage in patients with suspected COVID-19 infection admitted in ER. In addition, the visualization of early signs in specific areas could be a predictive marker of the severity of the disease. The objective of this project will be to study the association between the signs on lung ultrasound and the result of RT-PCR in patients with suspected COVID-19 infection in the ER.

Registry
clinicaltrials.gov
Start Date
April 28, 2020
End Date
July 20, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients admitted to Emergency Room for suspicion of COVID-19 infection with has a SARS-CoV-2 RT-PCR test and for whom the emergency doctor decide to perform a lung ultrasound

Exclusion Criteria

  • patients \< 18 years of age or under guardianship or curators,
  • pregnancy
  • poor echogenicity due to the presence of an acoustic barrier (pneumothorax, subcutaneous emphysema, etc.)
  • patients with a suspected or proven acute lung disease (pneumonitis, acute respiratory distress syndrome (ARDS))
  • chronic interstitial lung disease
  • patients who will refuse to give their consent.

Outcomes

Primary Outcomes

Lung ultrasound/biological correlation research modulating the severity of Covid-19 disease

Time Frame: 6 months

Polymerase chain reaction tests after reverse transcription for the detection of covid-19 viral RNA will be done as biological test.

Study Sites (1)

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