Study Results
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Basic Information
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UNKNOWN
NA
150 participants
INTERVENTIONAL
2007-11-30
2016-08-31
Brief Summary
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Each patient suffering from endophthalmitis must have immediately an ocular sampling, an intra ocular injection of antibiotics and a systemic antibiotic cover.
The etiological treatment will be adapted according to the infectious agent.
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Detailed Description
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This will help the ophthalmologist to be more efficient in accordance with the kind of the bacteria.
Data will also enable to compare both PCR techniques used in this study. The secondary goal of the prospective study is to characterize the resistance of bacterial's species found during acute endophthalmitis with the antibiogram and by the study of resistance genes, to enable to correlate the resistance in vitro with the therapeutic response in vivo and get precious epidemiological data to adapt prophylactic antibiotic.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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Endophthalmitis sufferers
Patients hospitalized for diagnostic and therapeutic evaluation of a post-operative acute endophthalmitis.
PCR : 16S ribosomal DNA and real-time targeted PCR
Sampling of aqueous humour
Healthy control patient
Patients hospitalized in the context of a scheduled surgery with sampling of aqueous humour.
PCR : 16S ribosomal DNA and real-time targeted PCR
Sampling of aqueous humour
Interventions
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PCR : 16S ribosomal DNA and real-time targeted PCR
Sampling of aqueous humour
Eligibility Criteria
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Inclusion Criteria
* Signed informed consent documentation
* Patients over 18 years
* Male or female person
* Patients hospitalized for diagnostic and therapeutic evaluation of a post-operative acute endophthalmitis, or within the context of a scheduled surgery with sampling of aqueous humour.
* Has given his or her consent, having been provided with detailed informations regarding to intraocular sampling.
Exclusion Criteria
* Patient's participation to the study refused
* Patients under 18 years
* Patients adults under guardianship or curatorship, or unable to express his/her consent.
* Pregnant women
* Breastfeeding women
* Person deprived of liberty
18 Years
ALL
Yes
Sponsors
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University Hospital, Grenoble
OTHER
Responsible Party
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Principal Investigators
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Christophe Chiquet, Doctor
Role: PRINCIPAL_INVESTIGATOR
Grenoble Hospital University
Locations
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UniversityHospitalGrenoble
La Tronche, , France
Countries
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Central Contacts
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Facility Contacts
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References
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Other Identifiers
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38RC07.006
Identifier Type: -
Identifier Source: org_study_id
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