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Completed

NCT Number: NCT05667207

Dipsticks and Microscopy to Reduce Antibiotic Use in Women's Urinary Tract Infections: a Pilot Trial (MicUTI)

With the aim to pilot a full-scaled trial to reduce unnecessary antibiotics in women with suspected uncomplicated urinary tract infections, twenty general practices in Bavaria, Germany, will be randomized to deliver patient management based on phase-contrast microscopy and urinary dipsticks or to usual care. Primary endpoints are recruitment and retention rates.

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Key information

Age range

18 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Stefanie Stark, Erlangen, Germany

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About this study

Introduction: Uncomplicated urinary tract infections (UTIs) in women are among the most common infections encountered in primary care after those of the respiratory tract. They are often self-limiting, even though antibiotics are prescribed for almost all women presenting with suggestive clinical features. Efforts directed to tackle antimicrobial resistance led to primary care randomized controlled trials (RCTs) that investigated alternative treatment strategies in these patients. While reducing antibiotic use substantially, none of the experimental treatments showed non-inferiority to antibiotics with respect to clinical outcomes such as symptom duration, symptom burden, and pyelonephritis. Evidence suggests that rapid point-of-care (POC) tests to detect bacteria and erythrocytes in urine at presentation may help primary care clinicians to select women with uncomplicated UTIs (unUTIs) in whom antibiotics can be withheld without affecting clinical outcomes. The aim of this study is to pilot a full-scaled primary care RCT to evaluate the effects of a POC diagnosis and treatment algorithm based on a combination of phase-contrast microscopy and urinary dipsticks on antibiotic use in women with symptoms of an unUTI.

Methods and analysis: MicUTI (Microscopy in UTI) is a pragmatic open-label two -arm parallel pilot cluster-RCT. Twenty general practices affiliated to the Bavarian Practice Based Research Network (BayFoNet) in Germany will be randomly assigned to deliver patient management based on POC-tests (POCTs) or to the usual care arm. Urine samples will be obtained at presentation for POCTs and microbiological analysis. All patients will be followed-up using a self-directed patient diary completed until day 7 from inclusion or until symptom resolution (up to day 14), and through telephone-calls at day 28. An electronic medical record review is performed in case of missing follow-up information.

Primary endpoints are patient enrollment and retention rates. Exploratory endpoints include antibiotic use for UTI at day 28, time to symptom resolution, symptom burden, the number of recurrent and upper UTIs and re-consultations, and diagnostic accuracy (POCTs vs. urine culture as reference standard).

Ethics, data protection and trial registration: The trial will be conducted in accordance to the declaration of Helsinki and the relevant data protection regulations. Institutional review board approval: 109/22-sc (December 16, 2022)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women with at least two of dysuria, frequency, urgency, lower abdominal pain or hematuria.

Exclusion criteria

  • Signs of a complicated UTI (anamnesis of fever, chills or flank pain)
  • Clinically relevant immunosuppression (i.e., current use of any immunosup-pressive therapy, congenital or acquired disorders of immunity)
  • Acute or chronic functional or anatomical variations in urinary tract except renal insufficiency grade II/IIIa
  • Permanent bladder catheter or use of bladder catheter within the past two weeks
  • UTI within the past two weeks
  • Use of any antibiotic within the past two weeks
  • Accommodation in a nursing home or hospital stay within the past two weeks
  • Severe neurologic or psychiatric illness, severe dementia or severe substance use disorder
  • Other severe diseases
  • Being unable to understand the informed consent or to complete the patient diary
  • Known pregnancy

Treatment and study plan

Point-of-care microscopy and dipstick guided management

Diagnostic Test

GPs will be encouraged to apply the following diagnosis and treatment algorithm (figure 1) to consenting women, taking their preferences into account:

  • If POCTs are positive for bacteria by microscopy and/or for erythrocytes by dipsticks the GP issues, at his/her own clinical judgement, a delayed or immediate prescription for an antibiotic.10 In the MicUTI intervention, delayed prescription is defined as issuing an antibiotic prescription with the advice to take the medication only when symptoms do not improve or worsen in 48 hours.
  • If POCTs are negative for bacteria and erythrocytes, the GP advises for self-help remedies according to guidelines and to do without antibiotics Study specific training in point-of-care microscopy will be provided to intervention practices.

Primary outcomes

  1. Recruitment efficacy

    Time frame: 6 months (duration of the trial in each study site)

    Number of participants enrolled per site over 6 months of trial duration

  2. Retention

    Time frame: 28 days (duration of the trial for each enrolled patient)

    Percentage of complete follow-ups over 28 days

Secondary outcomes

  1. Total antibiotic use

    Time frame: 28 days

    Number of antibiotic prescriptions per patient with UTI within 28 days

  2. Antibiotic doses

    Time frame: 28 days

    Defined daily doses of the prescribed antibiotics per patient with UTI within 28 days

  3. Inappropriate antibiotic use

    Time frame: Day 0

    Percentage of patients with symptoms of UTI who were prescribed antibiotics among those with negative urine cultures

  4. Immediate and delayed antibiotics

    Time frame: Day 0

    Number of immediate and delayed antibiotic prescriptions for uncomplicated UTI at initial consultation

  5. Early relapses

    Time frame: Days 0-14

    Number of early relapses of UTI (days 0-14)

  6. Recurrent urinary tract infections (UTIs)

    Time frame: Days 15-28

    Number of recurrent UTIs (day 15-28)

  7. Upper UTIs

    Time frame: 28 days

    Number of upper UTIs within 28 days

  8. Re-consultations

    Time frame: 28 days

    Number of consultations due to UTI (or symptoms of UTI) within 28 days

  9. Symptom resolution

    Time frame: Days 0-7 (or max. 14 if symptoms last longer)

    Time to symptom resolution defined as a maximum of 1 point in each of the UTI-SIQ-8 items

  10. Symptom Burden

    Time frame: Days 0-14

    Total symptom burden on days 0-7 (area under the curve of the UTI-SIQ-8 total symptom score)

  11. Diagnostic accuracy

    Time frame: Day 0

    Diagnostic accuracy of microscopy +/- dipstick compared to the standard (urine culture)

Sponsors and collaborators

Lead sponsor

Wuerzburg University Hospital

Other

Collaborators

  • LMU Klinikum
  • University Hospital Erlangen
  • University of Bristol
  • University of Georgia
  • University of Santiago de Compostela
  • University of Wuerzburg
  • Università degli Studi di Trento

Registry information

Official study title

Dipsticks and Point-of-care Microscopy to Reduce Antibiotic Use in Women With Uncomplicated Urinary Tract Infections: a Cluster-randomized Controlled Pilot Trial

Acronym: MicUTI

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Dec 28, 2022
Registry last updated
Jul 24, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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