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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03869580
Other study ID # P/2018/396
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 2019
Est. completion date December 2021

Study information

Verified date February 2019
Source Centre Hospitalier Universitaire de Besancon
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study was to determine the incidence and factors associated with double-J urinary stent infection.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 800
Est. completion date December 2021
Est. primary completion date April 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with a double-J stent placement or change in the hospital

Exclusion Criteria:

- renal transplants less than one year old

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU de Besançon Besançon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with urinary tract infection associated with double J stent Number of patients with urinary tract infection associated with double J stent 6 months
Primary Number of patients with specific clinical data associated with urinary tract infection associated with double J stent Clinical data (Age, sex, gender, comorbidities, indication of procedure, duration of double J stent placement) will be compared between patient with urinary tract infection and no urinary tract infection associated with double J stent 6 months
Secondary Number of patients with relapse and/or recurrence after a first urinary tract infection Number of patients with relapse and/or recurrence after a first urinary tract infection 6 months