Urinary Tract Infections Caused by Extended-spectrum Beta-lactamase-producing Enterobacteria
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Urinary Tract Infections. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Urinary Tract Infections Caused by Extended-spectrum Beta-lactamase-producing Enterobacteria: Management by General Practitioners in Bas-Rhin.
Overview
Urinary tract infections (UTIs) are one of the most common pathologies encountered in general practice. However, with increasing bacterial resistance to antibiotics, their treatment is becoming increasingly complex. Extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-E) pose a particular challenge due to their increased resistance to many commonly used antibiotics. The aim of this thesis is to study the management of such infections by general practitioners in Bas-Rhin and to suggest possible avenues for improvement.
Primary outcome measures
- Prescription rates of appropriate antibiotics for the treatment of ESBL-E UTIs [Time frame: Up to 1 year]
Eligibility criteria
Inclusion criteria
- Adult (≥18 years old)
- Subject with an Enterobacteriaceae urinary tract infection treated in a primary care setting for urinary tract infection between June 1, 2024 and December 31, 2024
- Subject not objecting, after being informed, to the reuse of their data for the purposes of this research.
- The subject's primary care physician agreeing to participate in the study
Exclusion criteria
- Subject and/or their primary care physician having expressed their opposition to participating in the study
- Subject under legal protection
- Subject under guardianship or curatorship
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
France · 1 center
- Service de maladies infectieuses et tropicales - Hôpitaux Universitaires de Strasbourg — Strasbourg
Identifiers
NCT: NCT06910878 · 9307