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NCT02851771 Clinical Trial

Improving the Diagnosis of Pneumonia in Emergency Rooms

Pneumonia Clinical Trial

Official title:
Improving the Diagnosis of Pneumonia in Emergency Rooms

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02851771
Other study ID # 2012-43
Secondary ID 2012-A01589-34
Status Completed
Phase N/A
First received
Last updated
Start date June 14, 2013
Est. completion date October 27, 2022

Study information
Verified date April 2023
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A point-of-care laboratory (POC) was set at North Hospital, Marseille, France for the diagnosis in less than two hours of pneumonia caused by known pathogens, close to the reception of Emergency service. In this instance 30% of patients have no etiological diagnosis after the POC tests Pneumonia. This lab has discovered over 200 new species of bacteria in humans, including vector bacteria and opened the field of large Deoxyribo Nucleic Acid (DNA ) viruses. Also, the laboratory of emerging viruses discovered many Ribo Nucleic Acid (RNA) viruses transmitted by arthropods. Based on this collection of new pathogens described in POC laboratory, this study proposes to expand the etiological diagnosis strategy of pneumonia after POC tests.

Recruitment information / eligibility
Status Completed
Enrollment 1364
Est. completion date October 27, 2022
Est. primary completion date April 15, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patient admitted at hospital for pneumonia requiring, for the emergency physician, a microbiological examination with a "POC pneumonia kit." - Patient who has freely signed the informed written consent - Patient affiliated to a social security scheme Exclusion Criteria: - Pregnant woman, parturient or nursing - Adult major under guardianship - Patient deprived of liberty under court order - Patient refusing or unable to sign the informed consent form.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Nasopharyngeal Swab

Locations
Country Name City State
France Assistance Publique Hopitaux de Marseille Marseille

Sponsors (1)
Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of patients in percentage with a confirmed etiological diagnosis of pneumonia 1 day
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