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Biofilms on Short-term Indwelling Ureteral Stents

C

Cantonal Hospital of St. Gallen

Status

Completed

Conditions

Ureteral Catheterization
Biofilm
Morbidity

Treatments

Other: Stent examination, urinary analysis, USSQ questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT02845726
CTU 15.010

Details and patient eligibility

About

This study is performed to analyze various aspects of biofilms on ureteral stents.

Full description

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.

Moreover, it could provide more detailed knowledge about the correlation of the occurrence of biofilms on ureteral stents and findings in urinary analysis, which could serve as a decision support whether patients with ureteral stents undergoing further interventions (for example ESWL or simple secondary URS) should receive antibiotic prophylaxis.

Correlation of results of urinary bacteriologies (assessed pre- and intraoperatively) and biofilm analysis on stents could provide information if "targeted antibiotic treatment" based on urinary bacteriology only is possible at all.

Correlation of urinary analysis and conventional urinary bacteriology could provide a valuable contribution regarding the prediction of bacteriuria and the necessity of postponing operations.

Additionally, the study is intended to provide an overview over the recent bacterial species that are involved into biofilms on ureteral stents and their resistance to antibiotics. This could provide valuable information about the choice of antibiotics in cases were treatment has to be performed empirically.

Enrollment

85 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients temporarily undergoing ureteral stenting
  • Informed consent

Exclusion criteria

  • Bilateral stenting
  • Ureteral obstruction due to malignancies
  • Additionally performed procedures/operations during stent indwelling time -Cognitively impaired patients
  • UTI at the time of stent insertion (>10 to the power of 2 cfu/ml)

Trial design

85 participants in 1 patient group

Patients with temporary ureteral stent
Description:
Assessment of patients transiently undergoing ureteral stenting.
Treatment:
Other: Stent examination, urinary analysis, USSQ questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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