Are the Patients Having Pets at Greater Risk of Carrying Multidrug Resistance Bacteriae?
NCT ID: NCT03352804
Last Updated: 2024-08-22
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
900 participants
OBSERVATIONAL
2017-06-12
2024-08-21
Brief Summary
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Aim : The primary objective is to study the association between the presence of a pet and the presence of a MDR bacteria. Methods : Cross sectional study will be performed in Reims University hospital in internal medicine ward.
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Detailed Description
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Aim : The primary objective is to study the association between the presence of a pet and the presence of a MDR bacteria.
Methods : Cross sectional study will be performed in Reims University hospital in internal medicine ward. Within the framework of the management of patients in internal medicine ward, all the hospitalized patients have systematically a screening of MDR Bacteriae. A questionnaire will be put handed to all the patients during their hospitalization as soon as they will be able to answer it. They will be informed about the objectives of the study. If the patient agrees to participate in the study, the questionnaire will be filled by every patient. It includes essentially closed questions and some open questions. A descriptive analysis will be performed. Bivariate analysis will be performed to investigate the relation between the presence of a pet and the presence of a MDR bacteria and clinical variables Multivariate logistic regression will be performed to investigate the factors independently related to the presence of a MDR bacteria.
Conditions
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Study Design
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CASE_CROSSOVER
CROSS_SECTIONAL
Study Groups
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Patients hospitalized in internal medicine ward
Patients included are patients hospitalized in internal medicine ward.
Screening of MDR Bacteriae
questionnaire will be filled by every patient
Interventions
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Screening of MDR Bacteriae
questionnaire will be filled by every patient
Eligibility Criteria
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Inclusion Criteria
* Patients who accepted to participate in the study
* \>18yo
Exclusion Criteria
* Patients coming from nursing home or institutionalized patients
* Patient who cannot communicated
18 Years
ALL
No
Sponsors
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CHU de Reims
OTHER
Responsible Party
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Locations
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Chu Reims
Reims, , France
Countries
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Other Identifiers
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PO17041*
Identifier Type: -
Identifier Source: org_study_id
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