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The Global Prevalence of Infections in Urology Study

The Global Prevalence of Infections in Urology Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03665467
Acronym
GPIU
Enrollment
2000
Registered
2018-09-11
Start date
2003-11-30
Completion date
2021-12-31
Last updated
2021-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hospital Infection, Urinary Tract Infections

Brief summary

Urology departments from all over the world are invited to join the Global Prevalence Study on Infections in Urology (GPIU-study) and the GPIU Prostate Biopsy Side Study. The GPIU study is taking part annually in November since 2003. European urologists were the first group of specialist to register hospital acquired infections on an international level. More than 20.000 patients have been screened and more than 2000 patients are currently listed in this database. Why? Infectious complications after urological procedures, such as prostate biopsy and increasing antimicrobial resistance are posing significant threats to modern urology The GPIU-study is a combined quality improvement initiative and a scientific study. Once the participating departments have filled in the report forms they will get access to statistics showing the accumulated results for all participating hospitals. The participants can anonymously compare their own results with hospitals from all over the World. The GPIU-study application has been designed as an instrument to ongoing follow-up of the development of important factors related to infection on international, national and local levels. Take responsibility for the future of urology - join the GPIU-studies! http://gpiu.esiu.org Prof. Dr. Florian M.E. Wagenlehner, MD, PhD Clinic for Urology, Pediatric Urology and Andrology University Clinic Giessen, Germany GPIU study coordinator Prof. Truls E. Bjerklund Johansen, MD, PhD Urology Department, Oslo University Hospital, Chairman ESIU Oslo, NO GPIU Study coordinator Zafer Tandogdu University College London (UCL), UK Dominic Althaus Software engineer Giessen, Ger

Interventions

None listed

Sponsors

European Association of Urology Research Foundation
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* On the chosen single study day at 08:00 AM local time all patients present on the ward of the participating institution are included * The presence of urinary tract infections (UTI) according to the CDC definitions during their entire hospital stay are documented and audited and the patients are categorized as having or not having a UTI and/or * The presence of surgical site infection (SSI) according to the CDC definitions during their entire hospital stay are documented and audited and the patients are categorized as having or not having a SSI

Design outcomes

Primary

MeasureTime frameDescription
Health care associated infection episodean infection onset 48 hours after admission to hospital or after an interventionHealth Care Associated Infections per definition of the Center for Disease Control

Countries

Germany, Hungary, Norway, United Kingdom

Contacts

Primary ContactFlorian Wagenlehner, Prof
Florian.Wagenlehner@chiru.med.uni-giessen.de+4916096018166
Backup ContactZafer Tandogdu, MD
drzafer@gmail.com07477473347

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026