Skip to content

Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure

Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure: Application to the COVID-19 Pandemic

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04534400
Acronym
QUANTICO-RETRO
Enrollment
1000
Registered
2020-09-01
Start date
2020-09-01
Completion date
2024-03-01
Last updated
2023-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Failure With Hypoxia, SARS-CoV-2 Infection

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 : 1. SARS-CoV-2 infections 2. Postoperative hypoxemic acute respiratory failure

Interventions

RADIATIONthoracic CT-scan

Automated measurement

Sponsors

VISIBLE PATIENT, E-MEDIA
CollaboratorUNKNOWN
University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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

Design outcomes

Primary

MeasureTime frame
Correlation between altered pulmonary volume and ordinal severity scale2 days after CT scan

Secondary

MeasureTime frame
Correlation between altered pulmonary volume and ordinal severity scale7 days after CT scan

Countries

France

Contacts

Primary ContactEric NOLL, MD
eric.noll@chru-strasbourg.fr33388127076
Backup ContactPierre DIEMUNSCH, MD
pierre.diemunsch@chru-strasbourg.fr33388125720

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026