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Extending Urine Analysis By Direct Mass Spectrometry

Primary Purpose

Urinary Tract Infection (Diagnosis)

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Conventional microbiological identification by culture plate
Direct mass spectrometry identification from urine sample
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Urinary Tract Infection (Diagnosis)

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of the Clinic for Internal Medicine at the University Hospital Basel with a suspected UTI and a minimum of one urine sample sent to the clinical microbiology laboratory.

Additionally at least one of the following:

  • Patients consented to the general (i.e. "hospital-wide") use of their data and samples for research purposes.
  • Patients consented to be enrolled in this study (by being informed about this study and signing the study specific consent form).
  • Patients who are exempted from the need for a consent by way of an exception in agreement to the decisions of the competent ethics committee.

Exclusion Criteria:

  • Minors or persons who declined the general use of their data and samples for research purposes (hospital wide consent) and declined or did not decide on the study specific consent form are not included.

Sites / Locations

  • University Hospital Basel

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional microbiological diagnostics

Conventional plus mass spectrometry

Arm Description

Conventional microbiological identification by culture plate (overnight cultures with subsequent bacterial/fungal identification).

Conventional microbiological identification by culture plate plus Direct mass spectrometry identification from urine sample. This additional diagnostic procedure is supplied additionally to conventional diagnostics.

Outcomes

Primary Outcome Measures

Time from the entry of a urine sample in the microbiological laboratory to the adequate/optimal/definitive treatment.

Secondary Outcome Measures

Time to diagnosis of a therapy relevant UTI.
Quantity of antibiotics prescribed per patient and ward.
Comparison of the length of hospital stay
Comparison of the number of possible complications connected to UTI

Full Information

First Posted
November 15, 2016
Last Updated
July 16, 2020
Sponsor
University Hospital, Basel, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT02966977
Brief Title
Extending Urine Analysis By Direct Mass Spectrometry
Official Title
Clinical Study To Analyse The Influence Of An Extended Urine Analysis By Mass Spectrometry On Internal Medicine Wards At The University Hospital Of Basel
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
October 3, 2016 (Actual)
Primary Completion Date
March 31, 2017 (Actual)
Study Completion Date
April 15, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to evaluate the effect of an extension of conventional urine diagnostics with mass spectrometry in patients with a suspected UTI. Mass spectrometry is done directly from the urine sample (without an intermediate bacterial culture).The primary outcome is the time from the entry of a urine sample in the microbiological laboratory to the adequate/optimal/definitive treatment. Secondary outcomes are the time to diagnosis of a therapy relevant UTI, the quantity of antibiotics prescribed per patient and ward and a comparison of the length of hospital stay.
Detailed Description
Urinary tract infections (UTI) have a high incidence rate and are one of the main reasons for initiating an antibiotic therapy, both, in the ambulatory and hospital setting. Mass spectrometry and improved sample preparation allows same-day identification of the causing agent of an UTI. This could shorten the time of suboptimal and potentially harmful empirical therapy. Additionally adverse effects from and the development of resistance against the applied antibiotic agent could be diminished. Matrix Assisted Laser Desorption Ionization (MALDI)- Time of Flight (TOF) Mass Spectrometry (MS) (MALDI-TOF MS) is already the preferred identification method in an increasing number of laboratories since it outperforms biochemical identification by speed and precision. This study tries to evaluate this new method to identify the causing agent of an UTI and evaluates its clinical implications. This research project is a clinical trial that intends to analyse urine of patients with suspected urinary tract infections by mass spectrometry. This patient material is conventionally processed and not retrieved particularly for study purposes. Health-related personal data is collected from patients on the wards of the Clinic for Internal Medicine at the University Hospital Basel that have a urine sample analysed during the study period. No health-related personal data is particularly collected for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infection (Diagnosis)

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
192 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional microbiological diagnostics
Arm Type
Active Comparator
Arm Description
Conventional microbiological identification by culture plate (overnight cultures with subsequent bacterial/fungal identification).
Arm Title
Conventional plus mass spectrometry
Arm Type
Experimental
Arm Description
Conventional microbiological identification by culture plate plus Direct mass spectrometry identification from urine sample. This additional diagnostic procedure is supplied additionally to conventional diagnostics.
Intervention Type
Other
Intervention Name(s)
Conventional microbiological identification by culture plate
Intervention Description
Conventional microbiological identification involves a step of overnight-2days growth of bacteria/fungi on culture plates prior to identification by biochemical methods or by mass spectrometry. See also information noted in arm/group description.
Intervention Type
Other
Intervention Name(s)
Direct mass spectrometry identification from urine sample
Intervention Description
The urine sample is concentrated and directly measured by a MALDI-TOF mass spectrometer without an intermediary microbiological culture on agar plates.
Primary Outcome Measure Information:
Title
Time from the entry of a urine sample in the microbiological laboratory to the adequate/optimal/definitive treatment.
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Time to diagnosis of a therapy relevant UTI.
Time Frame
1 week
Title
Quantity of antibiotics prescribed per patient and ward.
Time Frame
2 weeks
Title
Comparison of the length of hospital stay
Time Frame
2 weeks
Title
Comparison of the number of possible complications connected to UTI
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of the Clinic for Internal Medicine at the University Hospital Basel with a suspected UTI and a minimum of one urine sample sent to the clinical microbiology laboratory. Additionally at least one of the following: Patients consented to the general (i.e. "hospital-wide") use of their data and samples for research purposes. Patients consented to be enrolled in this study (by being informed about this study and signing the study specific consent form). Patients who are exempted from the need for a consent by way of an exception in agreement to the decisions of the competent ethics committee. Exclusion Criteria: Minors or persons who declined the general use of their data and samples for research purposes (hospital wide consent) and declined or did not decide on the study specific consent form are not included.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adrian Egli, PD Dr. FAMH
Organizational Affiliation
Clinical Microbiology, University Hospital Basel
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Basel
City
Basel
ZIP/Postal Code
4031
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

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Extending Urine Analysis By Direct Mass Spectrometry

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