Quantification of Radiological Pulmonary Involvement in Acute Respiratory Failure

SARS (Severe Acute Respiratory Syndrome) Clinical Trial

Official title:

Automated Quantification of Radiological Pulmonary Involvement in Acute Respiratory Failure

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04374734
• Other study ID #: 7791
• Status: Completed
• Start date: April 5, 2020
• Est. completion date: June 30, 2020

Study information

• Verified date: April 2020
• Source: University Hospital, Strasbourg, France
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Acute respiratory failure (ARF) is a common condition and a common reason for urgent medical consultation. Assessing the extent of respiratory impairment is important to improve the management of patients with ARF. When Acute respiratory failure is caused by pathology of the pulmonary parenchyma, quantification of pulmonary radiographic involvement may be a component of the initial assessment of severity. This radiographic quantification would only be usable in clinical routine if it can be automated and provide a real-time result.

The objective of this work is to assess the feasibility of an automated technique for quantifying radiological lung damage in situations of known or potential ARF.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: June 30, 2020
• Est. primary completion date: June 30, 2020
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients over 18 years of age

• Presenting a situation at risk of acute respiratory failure

• Requiring thorax imaging when they were treated.

Exclusion Criteria:

• Patients with anatomically incomplete thoracic imaging (e.g., technical acquisition error).

Related Conditions & MeSH terms

• Respiratory Insufficiency
• SARS (Severe Acute Respiratory Syndrome)
• Severe Acute Respiratory Syndrome

Locations

Country	Name	City	State
France	Service d' Anesthésie Réanimation Chirurgicale	Strasbourg

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Retrospective study of the relationship between severe forms of ARF and the extent of lung involvement		2 months