Nasal Carrying by Staphylococcus Aureus ST398 Strains in Community and Hospital Settings
NCT ID: NCT03869255
Last Updated: 2019-03-11
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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UNKNOWN
2000 participants
OBSERVATIONAL
2019-04-30
2020-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Hospitalized patients
Within 48 hours of admission to participating departments, all patiens will be included. A nasal swab will be performed within the first 48 hours and on the 7th day.
Nasal swab
In hospitalized patiens, a nasal swab will be performed within the first 48 hours and on the 7th day. In community patient, only one swab will be performed
Community patients
People coming to donate blood in "Etablissement Français du Sang" will be included and a nasal swab will be performed
Nasal swab
In hospitalized patiens, a nasal swab will be performed within the first 48 hours and on the 7th day. In community patient, only one swab will be performed
Interventions
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Nasal swab
In hospitalized patiens, a nasal swab will be performed within the first 48 hours and on the 7th day. In community patient, only one swab will be performed
Eligibility Criteria
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Inclusion Criteria
* age ≥ 18 years old
* No refusal of the person
* age ≥ 18 years old
* hospitalization in one of the services participating in the study
* no refusal of the person
Exclusion Criteria
For hospitalized patients :
* None
18 Years
ALL
Yes
Sponsors
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Centre Hospitalier Universitaire de Besancon
OTHER
Responsible Party
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Locations
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CHU de Besançon
Besançon, , France
Countries
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Other Identifiers
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API/2018/96
Identifier Type: -
Identifier Source: org_study_id
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