Antibiotic Bladder Instillations vs. Oral Suppression for the Treatment of Recurrent Urinary Tract Infections
Primary Purpose
Recurrent Urinary Tract Infection
Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Intravesical antibiotic instillation
Antibiotic oral suppressive therapy
Sponsored by
About this trial
This is an interventional prevention trial for Recurrent Urinary Tract Infection focused on measuring Antibiotic bladder instillation, Intravesical antibiotic instillation, Oral suppressive therapy, Recurrent UTI
Eligibility Criteria
Inclusion Criteria:
- Post-menopausal women with recurrent urinary tract infections (2 infections in a 6-month period or at least 3 infections in a 1-year period)
- Receiving estrogen vaginal therapy for 1 month prior to enrollment
- Able to come in to the office twice weekly for 3-4 weeks
- English speaking
- No allergy to at least one of the three antibiotics used for bladder instillations and at least one of the four antibiotics recommended for oral suppressive therapy.
- No uro-pathogen resistance to at least one of the three antibiotics used for bladder instillations and at least one of the four antibiotics recommended for oral suppressive therapy.
Exclusion Criteria:
- Allergy to all study antibiotics (Gentamicin, Tobramycin, Amikacin, Trimethoprim/sulfamethoxazole, Fosfomycin, Nitrofurantoin and Cephalexin)
- Recent Urine culture with pathogens resistant to all study antibiotics (Gentamicin, Tobramycin, Amikacin, Trimethoprim/sulfamethoxazole, Fosfomycin, Nitrofurantoin and Cephalexin)
- Renal failure (Creatinine clearance <30ml/min)
- History of urinary retention
- History of genitourinary structural abnormalities
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Intravesical antibiotic instillation
Oral antibiotic suppressive therapy
Arm Description
Outcomes
Primary Outcome Measures
The percentage of participants with urinary tract infections following treatment course
To compare the percentage of women developing urinary tract infections during the 3 months following treatment between the two groups.
Secondary Outcome Measures
The rate of antibiotic resistance of pathogens in participants developing urinary tract infections after completing the treatment course.
To compare the rate of antibiotic resistance of isolated pathogens when participants develop a urinary tract infection during the 3 months follow up period after intra-vesical antibiotic instillation vs. oral antibiotic suppressive therapy. the percentage of antibiotics on the susceptibility list of urine cultures will be compared between participants developing urinary tract infection in each group during the 3 months follow-up period after completing the treatment.
the percentage of patients developing side effects of the 2 treatments
To compare the percentage of patients developing side effects between the two treatment modalities. At their routine follow up visits patients will be asked about whether or not they developed side effects and the type and severity of side effects of the treatment received. The percentage of patients developing side effects (per type and severity) in each arm will be compared.
Full Information
NCT ID
NCT04285320
First Posted
February 17, 2020
Last Updated
January 13, 2021
Sponsor
Atlantic Health System
1. Study Identification
Unique Protocol Identification Number
NCT04285320
Brief Title
Antibiotic Bladder Instillations vs. Oral Suppression for the Treatment of Recurrent Urinary Tract Infections
Official Title
Intravesical Antibiotic Instillations Versus Oral Suppression for the Treatment of Recurrent Urinary Tract Infections in Post-menopausal Women
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 2021 (Anticipated)
Primary Completion Date
April 2023 (Anticipated)
Study Completion Date
April 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Atlantic Health System
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a research study that aims to determine if antibiotic bladder instillations (placing an antibiotic directly into the bladder) over several sessions at the office is a good option to prevent recurrent urinary tract infections, in comparison with oral suppression therapy (taking daily antibiotics in the form of pills by mouth). Oral antibiotic suppression therapy is currently the most common treatment route for recurrent urinary tract infections in post-menopausal women. The bladder antibiotic instillation may overcome the disadvantages of oral suppression therapy such as antibiotic resistance, certain side effects, and recurrence of infections after finishing the treatment course.
Detailed Description
In this study, the investigators aim to determine the effectiveness of intra-vesical antibiotic instillations for the prophylactic treatment of recurrent urinary tract infections in menopausal women in comparison with oral suppressive therapy. This is a parallel un-blinded randomized-controlled trial. the investigators will randomize post-menopausal women with recurrent urinary tract infections to either receive 6-8 intra-vesical antibiotic instillations at the office or to receive 3 months of oral antibiotic suppressive therapy.
In the bladder instillation arm, based on the participant's allergy and antibiotic resistance profile, one of the following three antibiotics will be instilled intravesically via a latex free BARD® 12 French Foley catheter for a total of 6-8 instillations (2 instillations/week) according to the Atlantic Health System Urogynecology Division antibiotic bladder instillation standard protocol:
Amikacin-30 mg in 60 ml of sterile water
Gentamycin-80mg in 60ml sterile water
Tobramycin-80 mg in 100 ml of sterile water
In the antibiotic oral suppression therapy arm, one of the following routinely used antibiotics will be prescribed for a total of 3 months according to the American Urogynecology Society Guidelines and based on the participant's allergy and antibiotic resistance profile:
Trimethoprim daily (100 mg)
Trimethoprim/sulfamethoxazole daily (40 mg/200 mg)
Trimethoprim/sulfamethoxazole every 3 days (40 mg/200 mg)
Nitrofurantoin monohydrate/macrocrystals daily (50 mg)
Nitrofurantoin monohydrate/macrocrystals daily (100 mg)
Cephalexin daily (125 mg)
Cephalexin daily (250 mg)
Fosfomycin every 10 days (3 grams) All medications used in this study are approved by the FDA to treat urinary tract infections.
Participants will be followed for total of 3 months after finishing either treatment course by only reviewing their medical records to collect data regarding development of urinary tract infections after treatment.
Primary endpoint/outcome:
• To compare the number of women developing urinary tract infections during the 3 months following treatment between the two groups.
Secondary endpoints/outcomes:
To compare the rate of antibiotic resistance of isolated pathogens after intravesical antibiotic instillation vs. oral antibiotic suppressive therapy
To compare side effects of the two treatment modalities
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Urinary Tract Infection
Keywords
Antibiotic bladder instillation, Intravesical antibiotic instillation, Oral suppressive therapy, Recurrent UTI
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intravesical antibiotic instillation
Arm Type
Active Comparator
Arm Title
Oral antibiotic suppressive therapy
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Intravesical antibiotic instillation
Intervention Description
Based on the participant's allergy and antibiotic resistance profile, one of the following three antibiotics will be instilled intravesically via a latex free BARD® 12 French Foley catheter for a total of 6-8 instillations (2 instillations/week) according to the Atlantic Health System Urogynecology Division antibiotic bladder instillation standard protocol:
Amikacin-30 mg in 60 ml of sterile water
Gentamycin-80mg in 60ml sterile water
Tobramycin-80 mg in 100 ml of sterile water
Intervention Type
Drug
Intervention Name(s)
Antibiotic oral suppressive therapy
Intervention Description
In the antibiotic oral suppression therapy arm, one of the following routinely used antibiotics will be prescribed for a total of 3 months according to the American Urogynecology Society Guidelines and based on the participant's allergy and antibiotic resistance profile:
Trimethoprim daily (100 mg)
Trimethoprim/sulfamethoxazole daily (40 mg/200 mg)
Trimethoprim/sulfamethoxazole every 3 days (40 mg/200 mg)
Nitrofurantoin monohydrate/macrocrystals daily (50 mg)
Nitrofurantoin monohydrate/macrocrystals daily (100 mg)
Cephalexin daily (125 mg)
Cephalexin daily (250 mg)
Fosfomycin every 10 days (3 grams)
Primary Outcome Measure Information:
Title
The percentage of participants with urinary tract infections following treatment course
Description
To compare the percentage of women developing urinary tract infections during the 3 months following treatment between the two groups.
Time Frame
Assessed starting immediately after the treatment is completed for a total of 3 months.
Secondary Outcome Measure Information:
Title
The rate of antibiotic resistance of pathogens in participants developing urinary tract infections after completing the treatment course.
Description
To compare the rate of antibiotic resistance of isolated pathogens when participants develop a urinary tract infection during the 3 months follow up period after intra-vesical antibiotic instillation vs. oral antibiotic suppressive therapy. the percentage of antibiotics on the susceptibility list of urine cultures will be compared between participants developing urinary tract infection in each group during the 3 months follow-up period after completing the treatment.
Time Frame
Assessed starting immediately after the treatment is completed for a total of 3 months
Title
the percentage of patients developing side effects of the 2 treatments
Description
To compare the percentage of patients developing side effects between the two treatment modalities. At their routine follow up visits patients will be asked about whether or not they developed side effects and the type and severity of side effects of the treatment received. The percentage of patients developing side effects (per type and severity) in each arm will be compared.
Time Frame
From the date of randomization until the date of first documented side effect assessed up to 3 months after the treatment is completed in each arm
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Post-menopausal women with recurrent urinary tract infections (2 infections in a 6-month period or at least 3 infections in a 1-year period)
Receiving estrogen vaginal therapy for 1 month prior to enrollment
Able to come in to the office twice weekly for 3-4 weeks
English speaking
No allergy to at least one of the three antibiotics used for bladder instillations and at least one of the four antibiotics recommended for oral suppressive therapy.
No uro-pathogen resistance to at least one of the three antibiotics used for bladder instillations and at least one of the four antibiotics recommended for oral suppressive therapy.
Exclusion Criteria:
Allergy to all study antibiotics (Gentamicin, Tobramycin, Amikacin, Trimethoprim/sulfamethoxazole, Fosfomycin, Nitrofurantoin and Cephalexin)
Recent Urine culture with pathogens resistant to all study antibiotics (Gentamicin, Tobramycin, Amikacin, Trimethoprim/sulfamethoxazole, Fosfomycin, Nitrofurantoin and Cephalexin)
Renal failure (Creatinine clearance <30ml/min)
History of urinary retention
History of genitourinary structural abnormalities
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Caroline Sabatino, MPH
Phone
973-971-7361
Email
caroline.sabatino@atlantichealth.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charbel Salamon, MD, MS
Organizational Affiliation
Atlantic Health System - Morristown Medical Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
31990805
Citation
Chernyak S, Salamon C. Intravesical Antibiotic Administration in the Treatment of Recurrent Urinary Tract Infections: Promising Results From a Case Series. Female Pelvic Med Reconstr Surg. 2020 Feb;26(2):152-154. doi: 10.1097/SPV.0000000000000810.
Results Reference
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Antibiotic Bladder Instillations vs. Oral Suppression for the Treatment of Recurrent Urinary Tract Infections
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