Multicentre Prospective Observational Cohort Study Aiming to Collect Medical Data, Create a Database to Facilitate Clinical and Fundamental Research Into Urinary Tract Infections With the Ultimate Goal of Improving Their Treatment.
The goal of this prospective observational study is to collect epidemiological, clinical, microbiological, genetic, and behavioral data on individuals with UTIs. The goal is to better understand which interventions are effective and, subsequently, to facilitate studies that will improve our understanding of the condition, enhance patient care and relief, and help combat antimicrobial resistance. This project will enable us to study episodes of urinary tract infections over a period of at least 2 years and up to 5 years.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Urinary symptoms/signs suggestive of UTI (as determined by investigators), or a history of such symptoms/signs.
Exclusion Criteria:
* Unwillingness to provide informed consent (for patients with capacity or for the representatives of those without capacity) and/or inability to provide informed consent (for patients without capacity and without representation).
Primary outcome measure(s)
Total number of suspected and microbiologically confirmed urinary tract infections. — From enrollment for a minimum of two years and a maximum of five years, with data collection at regular time points (2 months, 6 months, 12 months, 18 and 24 months after enrollment) Yearly incidence of suspected and microbiologically confirmed UTI at 12 months among all patients initially presenting with lower urinary tract symptoms (LUTS) or upper urinary tract symptoms (UUTS).
Trial sites (5)
Facility
City
Region
Status
Universitätsklinikum Frankfurt
Frankfurt
Germany
Leiden University Medical Center (LUMC)
Leiden
Netherlands
Hôpitaux Universitaires de Genève
Geneva
Canton of Geneva
Universitäts-Kinderspital beider Basel
Basel
Switzerland
Universitätsspital Zürich
Zurich
Switzerland
Official registry record
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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