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Urinary Tract Infections in Kidney Transplant Recipients

Urinary Tract Infections in Kidney Transplant Recipients : an Observational Cohort

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03211026
Acronym
URIKIT
Enrollment
120
Registered
2017-07-07
Start date
2017-05-04
Completion date
2024-05-04
Last updated
2021-04-14

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

Conditions

Kidney Transplantation

Keywords

Urinary tract infection, Multidrug resistant bacteria, Candiduria, Epidemiology, Graft rejection, Solid organ transplantation

Brief summary

The purpose of this study is to better estimate the prevalence of urinary tract infections (UTI) in kidney transplant (KIT) recipients, and especially multidrug resistant (MDR) bacteria. KIT recipients have a higher risk of UTI over the 6 first months following the transplantation. Urine culture was done in a city lab or at hospital. Current data on bacteriuria and candiduria lead mostly to hospital data that are incomplete..

Detailed description

The risk of UTI after a kidney transplantation is higher than in the general population. MDR bacteria, such as extended spectrum betalactamase (ESBL)-producing enterobacteriaceae or MDR Pseumomoas aeruginosa are emerging threats due to antibiotic selective pressure. Epidemiological data are mostly data from hospital laboratories that do not show a complete overview of the current situation. In addition, the different centers which participated to this study received before the beginning of the study a protocol to avoid carbapenem use. The main objective of this study is to assess the prevalence of MDR bacteria in an adult population of KIT recipients. Through this study, the management of UTI in KIT recipients will be improved. Data on bacteria or yeasts responsible for UTI (identification, resistance profile), antibiotic use, patients' outcome, and graft outcome will be collected.

Interventions

OTHERNo intervention

No intervention

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
Poitiers University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 year-old * Kidney transplanted for less than 5 years * First symptomatic episode of UTI with bacteria or yeast * To have a health insurance

Exclusion criteria

* Asymptomatic bacteriuria or candiduria * Protected people * Pregnant women -\> 2 bacteria in the urinalysis without external or internal urinary catheter

Design outcomes

Primary

MeasureTime frameDescription
Assessment of UTI due to MDR bacteriaDay 0 to 2 yearsProportion of MDR bacteria compared to other bacteria found in urinalysis of symptomatic KIT patients

Secondary

MeasureTime frameDescription
Risk factors for MDR UTIDay 0 to 2 yearsComparison of demographic and clinical characteristic of patients who develop an MDR versus a non-MDR UTI
Carbapenem use to treat UTIDay 0 to 2 yearsProportion of patients who received carbapenem for UTI treatment
Coherence between antibiotic protocol and treatment received to treat UTIDay 0 to 2 yearsProportion of patients who received carbapenem while responsible bacteria was susceptible to other antibiotics
UTI relapse frequencyDay 0 to 2 yearsProportion of patients with at least one relaspe of UTI with the same bacteria
Epidemiology of UTI in KIT recipientsDay 0 to 2 yearsFrequency of each bacteria or yeasts responsible for UTI
Assessment of kidney function during the observation periodDay 0 to 2 yearsDifference between the initial kidney function (MDRD) and the final kidney function at the end of the observation period
Graft outcomeDay 0 to 2 yearsNumber of patients needed a dialysis
Patients outcomeDay 0 to 2 yearsNumber of deaths
UTI recurrence frequency with a different micororganismDay 0 to 2 yearsProportion of patients with more than one UTI during the study period

Countries

France

Contacts

Primary ContactIsabelle PIRONNEAU
isabelle.pironneau@chu-poitiers.fr0549443203
Backup ContactFrançois ARRIVE
francois.arrive@gmail.com0630791699

Outcome results

None listed

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