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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02368847
Other study ID # UTI_UCP
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 9, 2015
Last updated February 17, 2015
Start date March 2015
Est. completion date December 2015

Study information

Verified date February 2015
Source Katholieke Universiteit Leuven
Contact Katrien Latour, MSc
Phone 003226425762
Email katrien.latour@kuleuven.be
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Interventional

Clinical Trial Summary

Urinary tract infections are one of the most common types of infections in older persons. The general aim of this study is to improve the epidemiological knowledge and develop a better diagnostic algorithm for urinary tract infections in older institutionalized individuals in order to reduce excessive prescribing of antibiotics and prevent antimicrobial resistance.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date December 2015
Est. primary completion date August 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- Older (65+ years) persons admitted to a gerontopsychiatric ward

Exclusion Criteria:

- Patients not understanding Dutch or not willing to participate (no informed consent)

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Device:
Diagnostic tests
C Reactive Protein (CRP) measurement on capillary blood using a point-of-care test to determine C Reactive Protein level in the blood
Diagnostic tests
Uricult dipslide: Easy-to-perform bacterial culture test for dectecting urinary tract infections in point of care settings

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Katholieke Universiteit Leuven

Outcome

Type Measure Description Time frame Safety issue
Primary Serious infection To verify if the elderly has a serious infection, the research team will combine test results (dipstick, dipslide and CRP measurement) with signs/symptoms reported in the patient questionnaire. 2 months No
Secondary Reliability of the uricult dipslide in a population of institutionalized older patients To verify the reliability of the uricult dipslide, a comparison will be made between the result of a dipslide read after 48h at room temperature, a dipslide incubated for 24h at +/- 35° Celsius and a urine culture test performed in a microbiology lab 2 months No
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