Evolution of Pulmonary Ultrasound in Patients Hospitalized for Covid (Coronavirus Disease) 19

Prospective Descriptive Study on the Evolution of Pulmonary Ultrasound in Patients Hospitalized for Covid19

Clinical thoracic ultrasound plays an important role in the exploration, diagnosis and follow-up of thoracic pathologies.

The COVID (Coronavirus Disease) epidemic is leading to a large influx of patients in the emergency department with respiratory disorders. The rapid diagnosis of respiratory disorders in infected patients is important for further management.

Chest ultrasound has already demonstrated its value in the diagnosis of pneumonia in the emergency department with superiority over chest X-ray.

However, there is little data on the thoracic ultrasound semiology of viral pneumonia in general and of COVID in particular.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Chest ultrasound has already shown its value in the diagnosis of pneumonia in the emergency department with superiority over chest X-ray.

However, there is little data on the thoracic ultrasound semiology of viral pneumonia in general and of COVID in particular.

Peng reported data from 20 patients and compared them to chest CT. The abnormalities are a thickening of the pleuropneumonia line, an interstitial syndrome with B lines, corresponding to frosted glass opacities, confluent B lines (snowstorm appearance) corresponding to interstitial infiltrate, sub-pleural alveolar opacities corresponding to sub-pleural condensations, more frank alveolar images corresponding to alveolar opacities. A multifocal aspect was associated with involvement of more than 2 lobes. However, the frequency of these abnormalities as well as the sensitivity of the echo are not detailed in this article.

Another Italian article describes a clinical case of COVID-19 pneumonia with sub-pleural involvement and irregularity of the pleuro-pulmonary line.

Clinical thoracic ultrasound has a major potential interest during the COVID epidemic: available at the patient's bedside, avoiding the need to move around, feasible for the physician during his visit, easy to clean especially if ultraportable devices are used, fast and not exposing the staff any more than the usual clinical examination.

In order to determine whether this technique is useful in the management of infected patients or patients suspected of COVID-19 infection with respiratory signs, we propose a descriptive prospective study evaluating the ultrasound semiology of COVID-19 pneumonia and the interest of ultrasound in the evolutionary follow-up of these patients.

Study Type

Observational

Enrollment (Actual)

106

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Amiens, France, 80054
        • CHU Amiens
      • Bayonne, France, 64109
        • CH de la Côte Basque
      • Boulogne-Billancourt, France, 92104
        • CHU Ambroise Pare
      • Caen, France, 14033
        • CHU caen
      • Chambéry, France, 73000
        • CHG de Chambery
      • Créteil, France, 94000
        • Centre Hospitalier Intercommunal de Créteil
      • Limoges, France, 87000
        • CHU de Limoges
      • Marseille, France, 13015
        • Aphm - Hopital Nord
      • Nancy, France, 54035
        • Chu de Nancy
      • Nîmes, France, 30029
        • CHU Nîmes
      • Orléans, France, 45100
        • CHR Orléans
      • Paris, France, 75679
        • CHU Cochin
      • Poitiers, France, 86021
        • CHU Poitiers
      • Rouen, France, 76038
        • CHU Rouen
      • Saint-Quentin, France, 02321
        • CH Saint-Quentin
      • Toulouse, France, 31059
        • CHU Larrey - Toulouse
      • Tours, France, 37000
        • CHU de Tours

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 105 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patient admitted to hospital with proven COVID-19 infection with respiratory signs and who need an hospitalization

Description

Inclusion Criteria:

  • Patients admitted to hospital with proven COVID-19 infection with respiratory signs warranting a chest CT scan

Exclusion Criteria:

  • Patient not agreeing to have his or her data collected for the study
  • Unconscious patient

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patient hospitalised with COVID-19 infection
Patients admitted to hospital with proven COVID-19 infection with respiratory signs warranting a chest CT scan
No special intervention : Ultrasound data will be collected

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Characteristics of pulmonary ultrasound for Covid-19 patients
Time Frame: Day one
description of ultrasound abnormalities for Covid-19 patients
Day one

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Characteristics of pulmonary ultrasound for Covid-19 patients
Time Frame: Day 3
description of ultrasound abnormalities for Covid-19 patients
Day 3
Characteristics of pulmonary ultrasound for Covid-19 patients
Time Frame: Day 14
description of ultrasound abnormalities for Covid-19 patients
Day 14
Charateristics of pulmonary CT-scan for Covid-19 patients
Time Frame: Day 1
description of CT-scan abnormalities for Covid-19 patients
Day 1
Charateristics of pulmonary CT-scan for Covid-19 patients
Time Frame: Day 3
description of CT-scan abnormalities for Covid-19 patients
Day 3
Charateristics of pulmonary CT-scan for Covid-19 patients
Time Frame: Day 14
description of CT-scan abnormalities for Covid-19 patients
Day 14

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 31, 2020

Primary Completion (Actual)

May 27, 2020

Study Completion (Actual)

June 30, 2020

Study Registration Dates

First Submitted

April 1, 2020

First Submitted That Met QC Criteria

April 9, 2020

First Posted (Actual)

April 10, 2020

Study Record Updates

Last Update Posted (Actual)

July 17, 2020

Last Update Submitted That Met QC Criteria

July 16, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on COVID-19

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