- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03352804
Are the Patients Having Pets at Greater Risk of Carrying Multidrug Resistance Bacteriae? (BRANITRANS)
Introduction : The multidrug resistance (MDR) Bacteriae are growing and are a public health problem. The known risk factors to be expanding of MDR Bacteriae are: taken antibiotics, hospitalization, journey in a country at risk. Other risk factors are emitted in hypothesis as the presence of pets.
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Introduction : The multidrug resistance (MDR) Bacteriae are growing and are a public health problem. The known risk factors to be expanding of MDR Bacteriae are: taken antibiotics, hospitalization, journey in a country at risk. Other risk factors are emitted in hypothesis as the presence of pets.
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.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Firouze BANI SADR
- Phone Number: 33 3.26.78.71.86
- Email: fbanisadr@chu-reims.fr
Study Locations
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-
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Reims, France, 51092
- Recruiting
- CHU Reims
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients who were screened for MDR bacteria
- Patients who accepted to participate in the study
- >18yo
exclusion criteria :
- Patient hospitalized before admission in our ward and having acquired a MDR bacteria in the course of care.
- Patients coming from nursing home or institutionalized patients
- Patient who cannot communicated
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Crossover
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients hospitalized in internal medicine ward
Patients included are patients hospitalized in internal medicine ward.
|
questionnaire will be filled by every patient
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Association between the presence of a pet and the presence of a MDR bacteria
Time Frame: Day0
|
Day0
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- PO17041
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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