- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02127450
Carbapenem-resistant Enterobacteriaceae: Prevalence, Risk Factors and Impact of the Use of the Phenotypic Algorithm for the Detection of Carbapenemases (E-CARB)
Study Overview
Status
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Clichy, France, 92110
- Hôpital Beaujon
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
- Patient hospitalised for more than 24 hours , with a clinical sample positive for a NS-CARB Enterobacteriaceae
- Patient hospitalised for more than 24 hours with clinical sample positive for a non-NS-CARB Enterobacteriaceae and hospitalised in the same type of ward as that case
- Patient hospitalised for more than 24 hours having had clinical sample(s) being stayed negative since the beginning of his admission and up to 3 days after the detection of the case, hospitalised in any type of ward in the hospital
Description
Inclusion Criteria:
- Case: Patient with a clinical sample positive for a NS-CARB Enterobacteriaceae
- Control 1: Patient with clinical sample positive for a non-NS-CARB Enterobacteriaceae and hospitalised in the same type of ward as that case
- Control 2: Patient having had clinical sample(s) being stayed negative since the beginning of his admission and up to 3 days after the detection of the case, hospitalised in any type of ward in the hospital
Exclusion Criteria:
- the patient with digestive ER-CARB
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Case: NS-CARB positive
Patient with a clinical sample positive for a NS-CARB Enterobacteriaceae
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Control 1: non-NS-CARB positive
Patient with clinical sample positive for a non-NS-CARB Enterobacteriaceae
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Control 2 : negative sample
Patient having had clinical sample(s) being stayed negative since the beginning of his admission and up to 3 days after the detection of the case
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Rate of CARB-NS isolates and among them the proportion of those producing CARBase.
Time Frame: 1 year
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Determining the prevalence rate of CARB-NS isolates and among them the proportion of those producing CARBase for all enterobacterial species and for each species. CARBase production will be determined by using in a phenotypic algorithm previously established on the basis on commercialized tests and by molecular methods. Determining by using a prospective case-control-control study the factors associated with a clinical sample positive for a NS-CARB isolate by distinguishing isolates non-CARBase-producing and isolates CARBase-producing.This study will be carried out during one year in 18 hospitals across France whose laboratory will participate in the prevalence study. The variables independently associated with a clinical sample positive for either a NS-CARB, non-CARBase-producing isolate or a NS-CARB, CARBase-producing isolate will be determined in a multivariate analysis. |
1 year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Detection of CARBase producing isolates as a measure of the diagnostic value of the phenotypic algorithm
Time Frame: 1 year
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Assessing the diagnostic value (sensitivity, specificity, positive predictive value and negative predictive value) of the phenotypic algorithm for the detection CARBase producing isolates by using the molecular methods as Gold standard method
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1 year
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Impact of the use of the phenotypic algorithm on the management of the patients identified as carrier of NS-CARB isolate.
Time Frame: 1 year
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Assessing the impact of the use of the phenotypic algorithm on the management of the patients identified as carrier of NS-CARB isolate (case) in the 18 hospitals : (i) time between the period at which the isolate is identified as NS-CARB and, on the one hand, knowledge acquisition by the Hygiene team and the medical staff of the presence of the case, and on the other hand, the period at which barrier precautions are implemented by distinguishing the type of barrier precautions implemented (standard or with dedicated non-medical staff) (ii) the duration of the implementation of barrier precaution with regard to the results concerning the production or the non-production of a CARBase by the NS-CARB isolate .
The results of this study will be compared with the results obtained during a previous study in which the phenotypic algorithm had not been used.
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1 year
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Collaborators and Investigators
Investigators
- Principal Investigator: Marie-Hélène Nicolas-Chanoine, MD, PhD, Assistance Publique - Hôpitaux de Paris
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NI 12025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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