Assessment of Longterm Ureteral Stenting

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

COMPLETED

Total Enrollment

91 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-07-31

Study Completion Date

2018-11-30

Brief Summary

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This study is performed to analyze various aspects of biofilms on ureteral stents in a longterm setting.

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Detailed Description

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The study is performed to provide a better understanding of the influence of biofilms on ureteral stents on the entire spectrum of stent-associated morbidity in a longterm setting.

In addition, the trial is intended to give an overview of the incidence of complaints, the occurrence of complications and their economic aspects.

The influence of biofilms on the morbidity associated with longterm ureteral stenting is assessed.

Conditions

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Longterm Indwelling Ureteral Stent

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients with longterm ureteral stent

Stent examination, urinary analysis, USSQ questionnaire

Intervention Type OTHER

Interventions

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Stent examination, urinary analysis, USSQ questionnaire

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with longterm indwelling ureteral stent (minimum of 2 months) undergoing regular changes
* Informed consent
* responsible patients

Exclusion Criteria

* ongoing therapy: OAB, LUTS, urinary incontinence, chronic prostatitis, chronic pelvic pain syndrome
* insufficient language skills
* cognitive limitation

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No