- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04341766
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
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Amiens, France, 80054
- CHU Amiens
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Bayonne, France, 64109
- CH de la Côte Basque
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Boulogne-Billancourt, France, 92104
- CHU Ambroise Pare
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Caen, France, 14033
- CHU caen
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Chambéry, France, 73000
- CHG de Chambery
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Créteil, France, 94000
- Centre Hospitalier Intercommunal de Créteil
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Limoges, France, 87000
- CHU de Limoges
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Marseille, France, 13015
- Aphm - Hopital Nord
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Nancy, France, 54035
- Chu de Nancy
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Nîmes, France, 30029
- CHU Nîmes
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Orléans, France, 45100
- CHR Orléans
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Paris, France, 75679
- CHU Cochin
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Poitiers, France, 86021
- CHU Poitiers
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Rouen, France, 76038
- CHU Rouen
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Saint-Quentin, France, 02321
- CH Saint-Quentin
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Toulouse, France, 31059
- CHU Larrey - Toulouse
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Tours, France, 37000
- CHU de Tours
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
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No special intervention : Ultrasound data will be collected
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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
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description of ultrasound abnormalities for Covid-19 patients
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Day one
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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
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Day 3
|
Characteristics of pulmonary ultrasound for Covid-19 patients
Time Frame: Day 14
|
description of ultrasound abnormalities for Covid-19 patients
|
Day 14
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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
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Day 14
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- COVID-ECHO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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