Clinical Trials in France / NCT05278390
Active, not recruiting
Not applicable
Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure: Application to the COVID-19 Pandemic
NCT05278390 · tracked via the Priya Life Science France tracker
Condition(s) studied
SARS-CoV-2 InfectionsRespiratory Failure With Hypoxia
Investigational drug(s) / intervention(s)
Thoracic CT scan
Thoracic CT scan: Automated quantitative analysis of altered pulmonary volume
Study 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
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
Primary outcome measure(s)
- Correlation between altered pulmonary volume and ordinal severity scale — 2 days after CT scan (Day 2)
This criterion will be expressed as a score between 1 (least severe) and 7 (most severe).
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Service d'anesthésie réanimation-CHU de Nancy | Nancy | France | |
| Service d'Anesthésie-Réanimation - CHU Strasbourg | Strasbourg | France |
More University Hospital, Strasbourg, France trials in France
Other trials for the same condition
Weaning From High Flow Nasal Oxygen in Acute Respiratory Failure : a Target Trial Emulation
Active, not recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05278390 on ClinicalTrials.gov ↗ ← All trials in France