- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04394026
Imaging Feature of SARS-CoV2 Infection (COVID19IF)
COVID-19 Imaging Features
Study Overview
Status
Conditions
Detailed Description
In March 2020, the third highest number of positive cases in the world was recorded in Italy, mainly due to 2 outbreaks of 2 different clusters in Lombardy and Veneto.
Fever is the most common symptom, followed by fatigue and dry cough; worsening of dyspnea and acute respiratory distress syndrome are found in severe cases. Previous reports have highlighted the key role of chest computed tomography (CT) and chest X-ray (CXR) in the diagnosis and follow-up of CoViD-19.
The most frequent clinical manifestation seems to be viral pneumonia, characterised by fever, cough, dyspnea. The severity of the disease varies widely: with evidence of mild disease in the majority of confirmed cases, severe pneumonia on a part of these, defined as dyspnea, hypoxia or lung involvement > 40% at imaging within 24-48 hours, and critical disease defined as respiratory failure, shock or multi-organ failure in particular patient cohorts.The mortality rate between cases ranges from approximately 4% in early reports to 14%, depending on the intensity of transmission and time of infection, and most fatal cases occurred in older patients or in patients with pre-existing medical co-morbidities.
Imaging plays an essential role in the diagnosis and follow-up of this infection.Several studies have been published describing the results of imaging, mainly using chest CT (computed tomography) with a limited number of articles describing disease in European patients or the possible different clinical/radiological presentation of the disease in European patients.
Pulmonary pathological findings appear to be similar to those previously described in SARS and MERS, with a prevalence of frosted glass densities and occasional consolidation.According to the literature, the 3 main features for the diagnosis of CoVid-19 pneumonia are: alveolar disease, represented by ground glass densities, bilateral distribution and prevalent peripheral involvement. This triad is more common in intermediate stages of the disease. In the early stages of the disease, a significant proportion of patients may present with negative or dubious X-rays and CT scans.There is an important overlap with imaging findings of other viral pneumonia, in particular with other members of the coronaviridae family: consolidation, however, seems to be less common in the early stages of CoViD-19 and bilateral distribution is less frequent in SARS and MERS pneumonia. Very little data have been published on the radiological evolution and modification of radiological aspects during infection: as the disease progresses, parenchymal consolidations begin to resorb and assume a frosted glass appearance. Another possible evolution is the progression towards the radiological aspect of the "white lung". This study aims to describe imaging aspects of CoViD-19 infection in Italian patients and the data on the radiological evolution.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Milano, Italy, 20132
- Deaprtment of Radiology, IRCCS Ospedale San Raffaele
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- CoViD-19 positive patients (rRT-PCR naso-pharyngeal swab)
- Suspicion of SARS-CoV2 on chest X-ray and/or chest CT presentation of disease
- Patients of all ages
- Subjects at risk (minors, patients in emergency situations, pregnant women, potentially incapable of giving their consent )
- Having signed the Informed Consent
Exclusion Criteria:
- Not fulfilling any of the above
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Other
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Describe qualitative and quantitative variables
Time Frame: Through study completion, an average of 5 months
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Evaluate RX imaging aspects at the time of diagnosis and until discharge.
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Through study completion, an average of 5 months
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Describe qualitative and quantitative variables
Time Frame: Through study completion, an average of 5 months
|
Evaluate CT imaging aspects at the time of diagnosis and until discharge.
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Through study completion, an average of 5 months
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Ability of imaging to predict disease progression
Time Frame: Through study completion, an average of 5 months
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Correlate imaging findings to OS
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Through study completion, an average of 5 months
|
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Ability of imaging to predict disease evolution
Time Frame: Through study completion, an average of 5 months
|
Correlate imaging findings over time
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Through study completion, an average of 5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Imaging findings and demographic data
Time Frame: Through study completion, an average of 5 months
|
Correlate imaging findings to age and sex
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Through study completion, an average of 5 months
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Imaging findings and laboratory exams
Time Frame: Through study completion, an average of 5 months
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Correlate imaging findings to laboratory values
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Through study completion, an average of 5 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Carlo Martinenghi, MD, IRCCS Ospedale San Raffaele
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 (Estimate)
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-19 IF
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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