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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03967210
Other study ID # KlebsieLCR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 5, 2019
Est. completion date January 13, 2020

Study information

Verified date August 2021
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Klebsiella pneumoniae is implicated in the occurrence of severe pneumonia. Most Klebsiella pneumoniae infections are associated with care and occur in patients with compromised immune defenses. More recently, cases of hepatic abscess and acute community meningitis related to strains of Klebsiella pneumoniae have been reported. The mortality of these infections is important, most often due to a delayed diagnosis. The poor prognostic factors reported in the literature for very low numbers are: advanced age, coma, septic shock, glyceryachia <10mg / dL and proteinuria> 750 mg / dL. In addition, no study has specifically focused on the factors of occurrence and factors associated with Klebsiella sp. Indeed, meningitis related to Klebsiella pneumoniae seems to be a rare but probably underestimated event whose risk factors, clinical presentation, microbiological are little known and the treatment modalities of this severe infection are not codified.


Recruitment information / eligibility

Status Completed
Enrollment 132
Est. completion date January 13, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Man or Woman whose age = 18 years - Patient with meningitis Klebsiella sp., hospitalized in one of the hospitals of the Clinical Microbiology Group - Francophone patient Exclusion Criteria: - Patient under tutorship or curatorship - Patient deprived of liberty - Patient under safeguard of justice - Patient opposing his participation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU Brest Brest
France CHU Caen Caen
France Hôpital henri Mondor Créteil
France CHU Lyon Lyon
France CHU Nantes Nantes
France CHU Nice Nice
France CHU Kremlin Bicetre Paris
France Groupe Hospitalier Paris Saint-Joseph Paris
France Hôpital Cochin Paris
France Hôpital Foch Paris
France Hôpital Lariboisière Paris
France Hôpital Necker Enfants Malades Paris
France Hôpital Sainte Anne Paris
France CHU Poitiers Poitiers
France CHU Reims Reims
France CHU Rennes Rennes
France CHU Strasbourg Strasbourg
France CHU Tours Tours

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Characterize meningitis with Klebsiella pneumoniae This corresponds to characterize Klebsiella pneumoniae meningitis, portal entry, secondary infection, associated antibiotic and associated therapies and the clinical course of patients. Day 1
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