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NCT05278390
Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure: Application to the COVID-19 Pandemic
Conditions: SARS-CoV-2 Infections, Respiratory Failure With Hypoxia
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 500
Sponsor: University Hospital, Strasbourg, France
Location: Service d'anesthésie réanimation-CHU de Nancy Nancy
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 aims at assessing the correlation between the amount of radiologic pulmonary alteration and the clinical severity in two clinical situation :
1. SARS-CoV-2 infections
2. Postoperative hypoxemic acute respiratory failure.
Eligibility Criteria
Inclusion Criteria:
* Subject admitted to a care unit of the University Hospitals of Strasbourg or the University Hospital of Nancy and presenting a suspicion of SARS-CoV-2 infection or postoperative hypoxemic respiratory failure
* Able to understand the objectives and risks of the research and to give dated and signed informed consent.
Subjects may also be included in emergency or immediate life-threatening situations.
* Subject with insurance covering
Exclusion Criteria:
* Pregnant woman (pregnancy confirmed by a urine or blood test)
* Subject usually on home oxygen therapy
* Subject under court protection
* Subject under guardianship or curatorship
Source: ClinicalTrials.gov (NCT05278390). StuddyBuddy aggregates publicly available trial information.