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Gentamicin Bladder Instillation Trial

Primary Purpose

Urinary Tract Infections

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Gentamicin
Placebo
Sponsored by
Gillette Children's Specialty Healthcare
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Urinary Tract Infections focused on measuring Urinary Tract Infections, Gentamicin

Eligibility Criteria

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

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.

Sites / Locations

  • Gillette Lifetime Specialty HealthcareRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Gentamicin

Placebo

Arm Description

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

Outcomes

Primary Outcome Measures

Symptomatic UTI
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

Asymptomatic UTI
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.

Full Information

First Posted
June 18, 2013
Last Updated
April 8, 2015
Sponsor
Gillette Children's Specialty Healthcare
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1. Study Identification

Unique Protocol Identification Number
NCT01884467
Brief Title
Gentamicin Bladder Instillation Trial
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 Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Unknown status
Study Start Date
May 2013 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
December 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Gillette Children's Specialty Healthcare

4. Oversight

Data Monitoring Committee
No

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infections
Keywords
Urinary Tract Infections, Gentamicin

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gentamicin
Arm Type
Experimental
Arm Description
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
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Drug: Normal saline; Dosage form: N/A; Dosage: 30 mL; Frequency: nightly bladder instillation; Duration: 1 year
Intervention Type
Drug
Intervention Name(s)
Gentamicin
Other Intervention Name(s)
Garamycin solution
Intervention Description
Comparison of Gentamicin versus placebo
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Symptomatic UTI
Description
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.
Time Frame
one year
Secondary Outcome Measure Information:
Title
Asymptomatic UTI
Description
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.
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients (>=16 years of age) with any diagnosis on IC of the bladder. Patients may catheterize either thru the urethra or a stoma (e.g. Mitrofanoff). A history of recurrent symptomatic UTI's (at least 3 per year). Patient must be able to travel to Gillette's Lifetime clinic for quarterly urine cultures Patient must have an "informed other" that can supplement any missing study information (incident UTI, treatment information, etc.) Exclusion Criteria: Patients currently on oral or intravesical antibiotic prophylaxis refusing to or not able to discontinue prophylaxis. Patients colonized with gentamicin-resistant bacteria on baseline urine culture or a gentamicin allergy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Meghan E Munger, MPH
Phone
651-229-1757
Email
MeghanEMunger@gillettechildrens.com
First Name & Middle Initial & Last Name or Official Title & Degree
Kari A Williams, MPH, CCRC
Phone
651-324-2316
Email
KariAWilliams@gillettechildrens.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sean P Elliott, MD, MS, FACS
Organizational Affiliation
Gillette Children's Specialty Healthcare
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gillette Lifetime Specialty Healthcare
City
Saint Paul
State/Province
Minnesota
ZIP/Postal Code
55130
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ronna Linroth, PhD
Phone
651-634-1920
Email
RLinroth@gillettechildrens.com
First Name & Middle Initial & Last Name & Degree
Sean P Elliott, MD, MS, FACS

12. IPD Sharing Statement

Learn more about this trial

Gentamicin Bladder Instillation Trial

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