Urinary Tract InfectionsPatients With Suprabubic CatheterPatients With Nephrostomy Catheter
Investigational drug(s) / intervention(s)
collection of bacterial strains
collection of bacterial strains: Urine (and blood) samples will be collected following SOC procedures for diagnostic purposes, at each visit of the patient (initial visit, follow up study or visit for new episode. For patients needing a catheter, urine sample will be collected before the insertion of the catheter, and before renewal of the catheter. Catheter tips will also be collected and sonicated to isolate bacteria. E. coli will be stored for analysis.
Study summary
Prospective study aiming at collecting clinical Escherichia coli isolates from patients with recurrent urinary tract infection; samples to be collected during routine procedures.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* patients hospitalized for urinary tract infection, with or without neurological disorders (spina bifida, MS, paraplegic patients) or ambulatory patients diagnosed with a urinary tract infection when the identified causative agent is E. coli
* patients who have or are planned to undergo the insertion of a suprapubic catheter
* patients who have or are planned to undergo the insertion a nephrostomy catheter
Exclusion Criteria: patients
* refusing the planned treatment
* with therapy compliance
* pregnant women
* who do not consent to participate
Primary outcome measure(s)
collection of longitudinal E. coli to be used for fundamental research — collection till the end of 2024 To collect longitudinal bacterial isolates of E. coli and to record clinical data for fundamental research about patients that are prone to developing urinary tract infections.
Trial sites (1)
Facility
City
Region
Status
Cliniques universitaires Saint Luc
Brussels
Belgium
Recruiting
More Université Catholique de Louvain trials in Belgium
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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