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CompletedNCT02851771Updated Apr 21, 2023

Improving the Diagnosis of Pneumonia in Emergency Rooms

An interventional study of Nasopharyngeal Swab in Pneumonia, sponsored by Assistance Publique Hopitaux De Marseille. Completed at 1 site in France. Per ClinicalTrials.gov, last updated 2023-04-21.

Sponsored by Assistance Publique Hopitaux De Marseille · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Registered 3 years 1 month after the study started (first participant enrolled Jun 2013, registered Jul 2016).
Phase
Not applicable
Study type
Interventional
Enrollment
1,364
Allocation
Not applicable
Sex
All
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Study 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.

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Conditions studied

  • Pneumonia
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In context

Pneumonia

2,044 studies on the registry are indexed under Pneumonia; 283 are open to participants now.

This study's enrollment of 1,364 is above the median of 106 across 1,247 interventional studies indexed under Pneumonia.

Browse Pneumonia studies →

Lead sponsor

Assistance Publique Hopitaux De Marseille is the lead sponsor of 686 studies on the registry; 148 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
1,364 participants (actual)

Study arms

  • Experimental
    Pneumonia Patients

    Patient admitted at hospital with pneumonia, who need a microbiological diagnosis

    Other: Nasopharyngeal Swab

Interventions

  • OtherNasopharyngeal Swab
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What researchers measure

Primary outcomes

  1. Number of patients in percentage with a confirmed etiological diagnosis of pneumonia

    Time frame: 1 day

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Study locations

1 site
  • Assistance Publique Hopitaux de Marseille
    Marseille, 13354, France
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 21, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02851771
Lead sponsor
Assistance Publique Hopitaux De Marseille
Responsible party
Sponsor
First posted
Aug 2, 2016
Start date
Jun 14, 2013
Primary completion
Apr 15, 2019
Completion
Oct 27, 2022
Last update
Apr 21, 2023

Study contacts

Catherine GEINDRE
study director · Assistance Publique Hôpitaux de Marseille
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

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