- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04534400
Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure (QUANTICO-RETRO)
Automated Quantification of Radiologic Pulmonary Alteration During Acute Respiratory Failure: Application to the COVID-19 Pandemic
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 Overview
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Eric NOLL, MD
- Phone Number: 33388127076
- Email: eric.noll@chru-strasbourg.fr
Study Contact Backup
- Name: Pierre DIEMUNSCH, MD
- Phone Number: 33388125720
- Email: pierre.diemunsch@chru-strasbourg.fr
Study Locations
-
-
-
Strasbourg, France, 67098
- Recruiting
- HÔPITAUX UNIVERSITAIRES DE STRASBOURG, Hôpital de Hautepierre, Service de Réanimation Médicale
-
Sub-Investigator:
- Francis VEILLON, MD
-
Principal Investigator:
- Eric NOLL, MD
-
Contact:
- Eric NOLL, MD
- Phone Number: 33388127076
- Email: eric.noll@chru-strasbourg.fr
-
Contact:
- Pierre DIEMUNSCH, MD
- Phone Number: 33388125720
- Email: pierre.diemunsch@chru-strasbourg.fr
-
Sub-Investigator:
- Pierre DIEMUNSCH, MD
-
Sub-Investigator:
- Julien POTTECHER, MD
-
Sub-Investigator:
- Mickaël OHANA, MD
-
Sub-Investigator:
- Francis SCHNEIDER, MD
-
Sub-Investigator:
- Bernard GOICHOIT, MD
-
Vandœuvre-lès-Nancy, France, 54500
- Not yet recruiting
- Hôpitaux Universitaires de Nancy Service d'anesthésie réanimation Hôpital de Brabois
-
Contact:
- Claude MEISTELMAN, MD
- Phone Number: 33383154166
- Email: c.meistelman@chru-nancy.fr
-
Sub-Investigator:
- Valérie CROISE-LAURENT, MD
-
Principal Investigator:
- Claude MEISTELMAN, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients with SARS-CoV-2 infection
|
Automated measurement
|
Patients with Postoperative hypoxemic respiratory failure
|
Automated measurement
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Correlation between altered pulmonary volume and ordinal severity scale
Time Frame: 2 days after CT scan
|
2 days after CT scan
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Correlation between altered pulmonary volume and ordinal severity scale
Time Frame: 7 days after CT scan
|
7 days after CT scan
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Respiration Disorders
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- Signs and Symptoms, Respiratory
- COVID-19
- Respiratory Insufficiency
- Hypoxia
Other Study ID Numbers
- 7888
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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