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

U

University Hospital, Strasbourg, France

Status

Enrolling

Conditions

SARS-CoV-2 Infections
Respiratory Failure With Hypoxia

Treatments

Radiation: Thoracic CT scan

Study type

Interventional

Funder types

Other

Identifiers

NCT05278390
8138

Details and patient eligibility

About

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.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

500 participants in 1 patient group

Thoracic CT Scan
Experimental group
Treatment:
Radiation: Thoracic CT scan

Trial contacts and locations

2

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Central trial contact

Eric NOLL, MD PhD

Data sourced from clinicaltrials.gov

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