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Targeted PCR and Acute Endophthalmitis

Contribution of Fast Molecular Bacterial Identification by Real-time PCR in Managing of Postoperative Acute Endophthalmitis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02850653
Acronym
Targeted PCR
Enrollment
150
Registered
2016-08-01
Start date
2007-11-30
Completion date
2016-08-31
Last updated
2016-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Endophthalmitis Post-operative

Keywords

Acute Endophthalmitis., PCR, Ocular sampling

Brief summary

Endophthalmitis is a serious eye infection of exogenous origin (post-operational, post-traumatic) or endogenous origin (metastatic). This is a diagnostic and therapeutic emergency. 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.

Detailed description

The main goal of this prospective multi-centre trial is to improve the sensitivity and rapidity of the infectious agent's identification involved in endophthalmitis cases, particularly virulent species (like Staphylococcus aureus, Streptococcus pneumoniae...) from ocular samples with the help of real-time PCR. 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.

Interventions

BIOLOGICALSampling of aqueous humour
BIOLOGICALPCR : 16S ribosomal DNA and real-time targeted PCR

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Subjects affiliated to the social security system * 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

* antibiotherapy via intravenous (\< 8 days) for patients NON suffering from endophthalmitis (control group) * 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

Design outcomes

Primary

MeasureTime frameDescription
Visual acuteness2 minutesClinical follow-up of patients
Intraocular pressure5 minutesClinical follow-up of patients
Biomicroscopic exam with the slit lamp3 minutesState of anterior and posterior segment (back of the eye)

Countries

France

Contacts

Primary ContactChristophe Chiquet, Doctor
CChiquet@chu-grenoble.fr04 76 76 55 48
Backup ContactMax Maurin, Professor
MMaurin@chu-grenoble.fr04 76 76 54 79

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026