NCT04534400RecruitingNot Applicable
Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure: Application to the COVID-19 Pandemic
University Hospital, Strasbourg, France2 sites in 1 country1,000 target enrollmentStarted: September 1, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 1,000
- Locations
- 2
- Primary Endpoint
- Correlation between altered pulmonary volume and ordinal severity scale
Study Overview
Brief Summary
Automated quantification of the pulmonary volume impaired during acute respiratory failure could be helpful to assess patient severity during COVID-19 infection or perioperative medicine, for example.
This study aim at assessing the correlation between the amount of radiologic pulmonary alteration and the clinical severity in two clinical situation :
- SARS-CoV-2 infections
- Postoperative hypoxemic acute respiratory failure
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •patient with insurance covering
- •patient admitted to the participating hospitals for SARS-CoV-2 infection or postoperative acute hypoxemic respiratory failure between 01/01/2019 and 05/11/2020
Exclusion Criteria
- •patient transferred to another hospital than the participating center during the 7 days following the CT scan
Outcomes
Primary Outcomes
Correlation between altered pulmonary volume and ordinal severity scale
Time Frame: 2 days after CT scan
Secondary Outcomes
- Correlation between altered pulmonary volume and ordinal severity scale(7 days after CT scan)
Investigators
Study Sites (2)
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