Ureteral Stent Exchange Abstention in Urinary Tract Infections

NCT ID: NCT06503588

Last Updated: 2025-08-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-07-01

Study Completion Date

2025-09-01

Brief Summary

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The Committee of Infectiology of the French Association of Urology (CIAFU) provided, for the first time in 2020, comprehensive guidelines for ureteral stent-associated urinary tract infections (USAUTI) prevention, diagnosis and treatment. Since evidence lacked in terms of appropriate treatment, guidelines could not support systematic change of US in case of USAUTI.

This study aims to evaluate whether "after guidelines group" patients treated for USAUTI had different occurrence of at least one relapse or recurrence than "before guidelines group".

Detailed Description

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Conditions

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Urinary Tract Infections Urinary Catheterization

Study Design

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Observational Model Type

OTHER

Study Time Perspective

RETROSPECTIVE

Study Groups

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Before guidelines

Patients treated for ureteral stent associated urinary tract infection in the University Hospital of Nancy from January 1, 2018 to May 31, 2020

No interventions assigned to this group

After guidelines

Patients treated for ureteral stent associated urinary tract infection in the University Hospital of Nancy from August 1, 2020 to December 31, 2022

Guidelines promoting surgical abstention

Intervention Type OTHER

Guidelines promoting surgical abstention

Interventions

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Guidelines promoting surgical abstention

Guidelines promoting surgical abstention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All patients with indwelling ureteral catheter
* AND confirmed or probable urinary tract infection

Exclusion Criteria

* Patient's opposition
* History of ileal conduit urinary diversion
* Second or more urinary tract infection during the study period
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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LEFEVRE Benjamin

MD. PhD.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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+33383154097 Lefevre, M.D. PhD

Role: PRINCIPAL_INVESTIGATOR

Central Hospital, Nancy, France

Locations

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Nancy university hospital

Nancy, Lorraine, France

Site Status RECRUITING

Countries

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France

Central Contacts

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Benjamin Lefevre, M.D. PhD

Role: CONTACT

+33383154097

Tahani Sara

Role: CONTACT

+33383154097

Facility Contacts

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Benjamin Lefevre, MD PhD

Role: primary

+33383154097

Other Identifiers

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2022PI037

Identifier Type: -

Identifier Source: org_study_id

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