Methenamine Hippurate Versus Trimethoprim in the Prevention of Recurrent UTIs
Primary Purpose
Urinary Tract Infections, Recurrent
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Trimethoprim
Methenamine hippurate
Sponsored by
About this trial
This is an interventional prevention trial for Urinary Tract Infections, Recurrent
Eligibility Criteria
Inclusion Criteria:
- recurrent UTI: at least 2 in the past 6 months or 3 in past year (culture positive)
- must have been symptomatic with dysuria, urgency, frequency, suprapubic pain, hematuria, malodorous urine
- treated for last UTI and negative urine culture on entry into study
- English speaking
Exclusion Criteria:
- pregnancy
- urinary tract abnormalities (eg kidney stones)
- acute pyelonephritis
- renal insufficiency or failure
- known allergy to medications
- prophylaxis for post-coital recurrent UTIs
Sites / Locations
- NorthShore Univeristy HealthSystem
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Patients with recurrent UTIs arm 1
Patients with recurrent UTIs arm 2
Arm Description
Patients are randomized to receive methenamine hippurate in one arm if they are diagnosed with recurrent urinary tract infections.
Patients are randomized to receive trimethoprim in the other arm if they are diagnosed with recurrent urinary tract infections.
Outcomes
Primary Outcome Measures
Time to Subsequent Infection as Defined From Time of Treatment Initiation to Recurrence of UTI
Patients will be advised to follow up with any symptoms of a recurrence or at 6 and 12 month intervals if symptom-free.
Recurrent UTI
The number of patient who had a recurrence of UTI within 12 months
Number of Infections
The number of infections at a 12 month follow up time period as defined by symptoms and positive urine culture.
Secondary Outcome Measures
Adverse Effects
The percentage of patients complaining of adverse effects of each medication, including dyspepsia, dysuria, rash, pruritus, nausea, epigastric pain, vomiting, glossitis, taste changes, fever, and photosensitivity.
Morisky Medication Adherence Survey
Morisky Medication Adherence Scale-8 (MMAS-8). Patient tolerability of medications using a tolerability survey. Minimum and maximum scores are 0 and 8 respectively. 0 means no adherence and 8 is maximal adherence. Low adherence corresponds to a score less than 6, medium adherence is between 6 and <8, and 8 is high adherence.
Bacterial Infection Prevalence and Types
Urine cultures and sensitivities for positive urine cultures
Full Information
NCT ID
NCT03077711
First Posted
February 27, 2017
Last Updated
January 10, 2020
Sponsor
NorthShore University HealthSystem
1. Study Identification
Unique Protocol Identification Number
NCT03077711
Brief Title
Methenamine Hippurate Versus Trimethoprim in the Prevention of Recurrent UTIs
Official Title
Methenamine Hippurate Versus Trimethoprim in the Prevention of Recurrent UTIs
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
June 2016 (Actual)
Primary Completion Date
June 21, 2019 (Actual)
Study Completion Date
June 21, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
NorthShore University HealthSystem
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Several methods are available for use in the prevention of recurrent urinary tract infections (UTIs) over the past few decades. These methods include suppressive antibiotics, estrogen cream, methenamine hippurate, d-mannose, cranberry, probiotics, and vitamin C. Of these, the majority of the literature is in favor of use of suppressive antibiotics for preventing UTIs. However, this data is now about 10 years old. Increasing use of antibiotics over the years has lead to increased resistance of bacteria. In addition, long-term antibiotic use has several adverse effects, some life-threatening. There is recent literature evaluating the use of several of the alternatives to suppressive antibiotics with mixed results. A comparative study of the efficacy of methenamine hippurate to suppressive antibiotics is lacking in the current literature. Several early partly-randomized trials done with methenamine hippurate have shown promising results, but are only as recent as 1987. The primary objective of this prospective, randomized study is to determine whether there is a significant difference in the prevention of recurrent UTIs when given either methenamine hippurate or daily suppressive antibiotics. The secondary objective of this study is to determine how well patients are able to tolerate each of these medications and what adverse effects are observed in a given 1 year time period. The long-term goals of this study are to find an alternative to using suppressive antibiotics, potentially with a lower adverse effect profile and less of the dangers of long term antibiotic use. Finding an alternative to suppressive antibiotics would also tackle the issue of antibiotic resistance.
Detailed Description
Hypothesis:
The hypothesis of this study is that the group taking trimethoprim will have a lower recurrence rate than those taking methenamine hippurate based on the literature. The investigators aim to identify to what degree that difference is and whether or not it is an acceptable difference given the greater degree of an antibiotic resistance.
Objectives:
The primary objective of this prospective, randomized study is to determine whether there is a significant difference in the prevention of recurrent UTIs when given either methenamine hippurate or daily suppressive antibiotics independent of vaginal estrogen use.
The secondary objective of this study is to determine how well patients are able to tolerate each of these medications and what adverse effects are observed in a 1 year time period.
Specific Aims:
Identify if there is a differential impact on prevention of recurrent UTIs when treated with either trimethoprim or methenamine hippurate in a 6 and 12 month period.
Identify adverse reactions in each group.
Determine whether or not estrogen has a more additive effect to trimethoprim or methenamine hippurate in post-menopausal women.
Identify how well tolerated the study medications are and whether or not the size of the pills or the frequency of taking them prevents patients from continuing therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infections, Recurrent
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Patients diagnosed with recurrent urinary tract infections are recruited into this study.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
92 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patients with recurrent UTIs arm 1
Arm Type
Active Comparator
Arm Description
Patients are randomized to receive methenamine hippurate in one arm if they are diagnosed with recurrent urinary tract infections.
Arm Title
Patients with recurrent UTIs arm 2
Arm Type
Active Comparator
Arm Description
Patients are randomized to receive trimethoprim in the other arm if they are diagnosed with recurrent urinary tract infections.
Intervention Type
Drug
Intervention Name(s)
Trimethoprim
Other Intervention Name(s)
Trimpex
Intervention Description
suppressive antibiotic. Estrogen cream may be prescribed if the patient is post-menopausal (but not as a part of this study).
Intervention Type
Drug
Intervention Name(s)
Methenamine hippurate
Other Intervention Name(s)
Hiprex
Intervention Description
antiseptic used in the prevention of recurrent UTIs. Estrogen cream may be prescribed if the patient is post-menopausal (but not as a part of this study).
Primary Outcome Measure Information:
Title
Time to Subsequent Infection as Defined From Time of Treatment Initiation to Recurrence of UTI
Description
Patients will be advised to follow up with any symptoms of a recurrence or at 6 and 12 month intervals if symptom-free.
Time Frame
up to 12 months
Title
Recurrent UTI
Description
The number of patient who had a recurrence of UTI within 12 months
Time Frame
up to 12 months
Title
Number of Infections
Description
The number of infections at a 12 month follow up time period as defined by symptoms and positive urine culture.
Time Frame
up to 12 months
Secondary Outcome Measure Information:
Title
Adverse Effects
Description
The percentage of patients complaining of adverse effects of each medication, including dyspepsia, dysuria, rash, pruritus, nausea, epigastric pain, vomiting, glossitis, taste changes, fever, and photosensitivity.
Time Frame
up to 12 months
Title
Morisky Medication Adherence Survey
Description
Morisky Medication Adherence Scale-8 (MMAS-8). Patient tolerability of medications using a tolerability survey. Minimum and maximum scores are 0 and 8 respectively. 0 means no adherence and 8 is maximal adherence. Low adherence corresponds to a score less than 6, medium adherence is between 6 and <8, and 8 is high adherence.
Time Frame
up to 12 months
Title
Bacterial Infection Prevalence and Types
Description
Urine cultures and sensitivities for positive urine cultures
Time Frame
up to 12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
recurrent UTI: at least 2 in the past 6 months or 3 in past year (culture positive)
must have been symptomatic with dysuria, urgency, frequency, suprapubic pain, hematuria, malodorous urine
treated for last UTI and negative urine culture on entry into study
English speaking
Exclusion Criteria:
pregnancy
urinary tract abnormalities (eg kidney stones)
acute pyelonephritis
renal insufficiency or failure
known allergy to medications
prophylaxis for post-coital recurrent UTIs
Facility Information:
Facility Name
NorthShore Univeristy HealthSystem
City
Skokie
State/Province
Illinois
ZIP/Postal Code
60076
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
The investigators are currently only recruiting at one institution and only researchers on the original institutional review board will have access to data. Only the principal investigator and research coordinator will have the data to be analyzed.
Learn more about this trial
Methenamine Hippurate Versus Trimethoprim in the Prevention of Recurrent UTIs
We'll reach out to this number within 24 hrs