Detection of Colistin-resistant Isolates From Patients of Intensive Care Units and Oncohaematology Wards.
NCT ID: NCT03971877
Last Updated: 2022-03-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
1934 participants
OBSERVATIONAL
2019-12-16
2021-02-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Patients admitted in ICU or oncohaematology ward
Rapid Polymyxin NP test
From rectal swabs of patients admitted in ICU and oncohaematology ward, investigators will use first a new culture medium (SuperPolymyxin) for screening the colistin resistant Gram negative and then a new rapid test (Rapid Polymyxin NP test) to confirm this resistance. These tests will be compared to the reference test of MIC (Minimal Inhibitory Concentration) determined by the broth micro-dilution (BMD) method.
Interventions
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Rapid Polymyxin NP test
From rectal swabs of patients admitted in ICU and oncohaematology ward, investigators will use first a new culture medium (SuperPolymyxin) for screening the colistin resistant Gram negative and then a new rapid test (Rapid Polymyxin NP test) to confirm this resistance. These tests will be compared to the reference test of MIC (Minimal Inhibitory Concentration) determined by the broth micro-dilution (BMD) method.
Eligibility Criteria
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Inclusion Criteria
* patients admitted in ICU or in oncohaematology ward
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Bordeaux
OTHER
Responsible Party
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Principal Investigators
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Paul PEREZ, MD-PhD
Role: STUDY_CHAIR
Unité de Soutien Méthodologique à la Recherche Clinique et Epidémiologique (USMR) du CHU de Bordeaux
Locations
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CHU de Bordeaux
Bordeaux, , France
CH de Dax
Dax, , France
CHU de Limoges
Limoges, , France
CH de Mont de Marsan
Mont-de-Marsan, , France
Countries
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Other Identifiers
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CHUBX 2016/45
Identifier Type: -
Identifier Source: org_study_id
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