Gentamicin Bladder Instillation Trial

Sponsor
Gillette Children's Specialty Healthcare (Other)
Overall Status
Unknown status
CT.gov ID
NCT01884467
Collaborator
(none)
24
1
2
43
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Study Details

Study Description

Brief Summary

Recurrent UTIs are common among patients on IC. These create significant patient morbidity and healthcare burden. In desperation, many physicians prescribe prophylactic oral or intravesical antibiotics. This practice is common among our Gillette clinic patients. However, the benefit is unclear and the risks are not insignificant. As such, practice variation is significant. In order to better define the evidence for or against gentamicin bladder irrigation and thus inform clinical practice both locally at our Gillette urology clinic and for practitioners at large we will pursue the following specific aims:

  1. Compare rates of symptomatic urinary tract infection and asymptomatic bacteriuria among a population of Gillette patients on IC with and without gentamicin bladder instillation.

  2. Compare antibiotic resistance rates among a population of Gillette patients on IC with and without gentamicin bladder instillation.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

In the Gillette Lifetime Urology clinic, gentamicin bladder instillation (GBI) for UTI prophylaxis is common practice among our neurogenic bladder patients in IC. However, as previously shown, the evidence supporting this practice is mixed. Potential risks of this practice include wasted costs, wasted materials, wasted time and growing antibiotic resistance. Potential benefits include reduced use of systemic antibiotics, a reduction in symptomatic UTIs and fewer hospitalizations for febrile UTIs. We seek to define the evidence for or against this practice by completing a double-blind randomized controlled trial of GBI vs. NS instillation. Such a trial would benefit our Gillette patients and the community of patients on IC worldwide.

Recurrent UTIs are common among patients on IC. These create significant patient morbidity and healthcare burden. In desperation, many physicians prescribe prophylactic oral or intravesical antibiotics. This practice is common among our Gillette clinic patients. However, the benefit is unclear and the risks are not insignificant. As such, practice variation is significant. In order to better define the evidence for or against gentamicin bladder irrigation and thus inform clinical practice both locally at our Gillette urology clinic and for practitioners at large we will pursue the following specific aims:

  1. Compare rates of symptomatic urinary tract infection and asymptomatic bacteriuria among a population of Gillette patients on IC with and without gentamicin bladder instillation.

  2. Compare antibiotic resistance rates among a population of Gillette patients on IC with and without gentamicin bladder instillation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
Randomized Placebo-Controlled Trial of Gentamicin Bladder Instillation for the Prevention of Urinary Tract Infection in Adults at High Risk for Cystitis Due to Intermittent Catheterization
Study Start Date :
May 1, 2013
Anticipated Primary Completion Date :
Dec 1, 2015
Anticipated Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Gentamicin

Intervention: Gentamicin; Dosage form: 120mg reconstituted in 250cc of normal saline; Dosage: 30mL; Frequency: nightly instillation into bladder (to remain overnight until draining it out in morning); Duration: 1 year

Drug: Gentamicin
Comparison of Gentamicin versus placebo
Other Names:
  • Garamycin solution
  • Placebo Comparator: Placebo

    Drug: Normal saline; Dosage form: N/A; Dosage: 30 mL; Frequency: nightly bladder instillation; Duration: 1 year

    Drug: Placebo

    Outcome Measures

    Primary Outcome Measures

    1. Symptomatic UTI [one year]

      Our primary outcome will be febrile or symptomatic UTI, defined as fever or abdominal pain or new bladder symptoms such as pain, urinary incontinence, hematuria or more frequent bladder spasms plus urine culture demonstrating >103 CFUs of a single dominant bacteria or >105 of multiple bacteria.

    Secondary Outcome Measures

    1. Asymptomatic UTI [one year]

      A quarterly urine culture will be performed at Gillette's Lifetime Clinic to assess asymptomatic bacteriuria. Asymptomatic bacteriuria will be defined as an asymptomatic patient with urine sample culture positive for typical bacteria.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    16 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients (>=16 years of age) with any diagnosis on IC of the bladder.

    2. Patients may catheterize either thru the urethra or a stoma (e.g. Mitrofanoff).

    3. A history of recurrent symptomatic UTI's (at least 3 per year).

    4. Patient must be able to travel to Gillette's Lifetime clinic for quarterly urine cultures

    5. Patient must have an "informed other" that can supplement any missing study information (incident UTI, treatment information, etc.)

    Exclusion Criteria:
    1. Patients currently on oral or intravesical antibiotic prophylaxis refusing to or not able to discontinue prophylaxis.

    2. Patients colonized with gentamicin-resistant bacteria on baseline urine culture or a gentamicin allergy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Gillette Lifetime Specialty Healthcare Saint Paul Minnesota United States 55130

    Sponsors and Collaborators

    • Gillette Children's Specialty Healthcare

    Investigators

    • Principal Investigator: Sean P Elliott, MD, MS, FACS, Gillette Children's Specialty Healthcare

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sean P. Elliott, M.D., M.S., Associate Professor and Vice Chair, Director of Reconstructive Urology, University of Minnesota, Gillette Children's Specialty Healthcare
    ClinicalTrials.gov Identifier:
    NCT01884467
    Other Study ID Numbers:
    • 1210M21603
    First Posted:
    Jun 24, 2013
    Last Update Posted:
    Apr 9, 2015
    Last Verified:
    Apr 1, 2015
    Keywords provided by Sean P. Elliott, M.D., M.S., Associate Professor and Vice Chair, Director of Reconstructive Urology, University of Minnesota, Gillette Children's Specialty Healthcare
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 9, 2015