Bacterial Interference for Preventing Recurrent Urinary Tract Infection - New Ways of Treatment (BIrUTI)
Primary Purpose
Recurrent Urinary Tract Infections
Status
Not yet recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
ABU bladder lavage
Saline bladder lavage
Sponsored by
About this trial
This is an interventional prevention trial for Recurrent Urinary Tract Infections focused on measuring rUTI, E.coli, prophylactic, bladder lavage
Eligibility Criteria
Inclusion Criteria:
- Diagnosed with recurrent cystitis including 2 times of rUTI within the last 6 months or 3 times in the last 12 months, where at least 2 cultures show the same bacteria.
- Normal investigation for lower urinary tract diseases (LUTD) including voiding diary, symptom scores, flexible cystoscopy, voiding diagram and test for residual urine.
- Failed previously treatments.
- Patients with native bladder with both spontaneous voiding, the need for clean intermittent catheter (CIC) or indwelling catheter.
- Patients with neurogenic and non-neurogenic bladder dysfunction.
- Patients with urostomy, kidney transplantation or another complicated genesis.
- Written consent.
Exclusion Criteria:
- Malignancy in the urinary tract, kidney-, ureteral- or bladder stones, age < 18 years, pregnancy, breastfeeding. Patients in ongoing orally antibiotic treatment. Not able to speak or understand Danish.
Sites / Locations
- Odense university hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Patients prophylatic treated with ABU
Patients control group
Arm Description
Patients with prophylactic bladder flushing with an ABU strain.
The control group with bladder flushing with saline solution.
Outcomes
Primary Outcome Measures
The number of events (symptomatic UTIs) in the follow-up period
The number of prescriptions or hospital visits
Secondary Outcome Measures
Time to first symptomatic UTI after the intervention
Symptoms and the need for medical treatment or hospitalisation
Quality of life by standard Questionnaires_ICIQ-LUT
ICIQ-LUTSqol 08/04 questionnaire evaluating quality of life (QoL) in urinary incontinent patients (overall score with greater values indicating increased symptom severity)
Quality of life by standard Questionnaires_SF36
SF-36 (scored so that a high score defines a more favorable health state)
EQ-5D-5L
Questionnaire evaluating quality of life at 5 terms (mobility, self-care, usual activities, pain, discomfort and anxiety/depression)
CRF
Case report form with respect to urinary/bladder symptoms, odour, perfomancestatus ect)
Hospitalization
Hospital visit
Complications (bleeding, pain)
Complications due to bladder lavage
Microbiological diagnostics: Etiology, resistance
Measurements during treatment protocol
Full Information
NCT ID
NCT04846803
First Posted
April 12, 2021
Last Updated
December 17, 2022
Sponsor
Odense University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04846803
Brief Title
Bacterial Interference for Preventing Recurrent Urinary Tract Infection - New Ways of Treatment
Acronym
BIrUTI
Official Title
Bacterial Interference for Preventing Recurrent Urinary Tract Infection - New Ways of Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2023 (Anticipated)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Odense University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Urinary tract infection (UTI) is one of the most common bacterial infections worldwide. It affects 150 million people annually. Treatment of patients with UTI entails a high consumption of antibiotics and large social and health costs. With this protocol, we want to elucidate alternative treatment methods for especially recurrent urinary tract infection. Bacteria have internal competitiveness (bacterial interference) and it is known that the non-pathogenic E.coli can outcompete the pathogenic E.coli in laboratory studies.
We intend to strengthen the clinical evidence that it can be used as patient treatment through a clinical, placebo-controlled, double-blind trial at Odense University Hospital.
Detailed Description
Urinary tract infection (UTI) is one of the most common bacterial infections worldwide. It affects 150 million people annually. Treatment of patients with UTI entails a high consumption of antibiotics and large social and health costs. With this protocol, we want to elucidate alternative treatment methods for especially recurrent urinary tract infection. Bacteria have internal competitiveness (bacterial interference) and it is known that the non-pathogenic E.coli can outcompete the pathogenic E.coli in laboratory studies.
We intend to strengthen the clinical evidence that it can be used as patient treatment through a clinical, placebo-controlled, double-blind trial at Odense University Hospital.
Claim to be investigated:
The non-pathogenic bacterial strain (ABU) E.coli can overcome the most common pathogenic E.coli (UPEC) in humans.
ABU can be used for preventive treatment in patients with recurrent urinary tract infections.
Clinical effect of preventive treatment (prophylactic treatment) with the non-pathogenic bacterial strain (ABU) in a selected group of patients with recurrent cystitis: A clinical, placebo-controlled, triple-blinded study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Urinary Tract Infections
Keywords
rUTI, E.coli, prophylactic, bladder lavage
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Inclusion with 6 months observation (standard treatment). Randomisation in ratio 3:1 for treatment initiation at baseline.
Patients with prophylactic bladder flushing with an ABU strain.
The control group with saline bladder flushing .
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Patients prophylatic treated with ABU
Arm Type
Experimental
Arm Description
Patients with prophylactic bladder flushing with an ABU strain.
Arm Title
Patients control group
Arm Type
Placebo Comparator
Arm Description
The control group with bladder flushing with saline solution.
Intervention Type
Biological
Intervention Name(s)
ABU bladder lavage
Intervention Description
Clinical effect of preventive treatment (prophylactic treatment) - bladder lavage with the non-pathogenic bacterial strain (ABU)
Intervention Type
Biological
Intervention Name(s)
Saline bladder lavage
Intervention Description
Clinical effect of preventive treatment (prophylactic treatment) - bladder lavage with saline
Primary Outcome Measure Information:
Title
The number of events (symptomatic UTIs) in the follow-up period
Description
The number of prescriptions or hospital visits
Time Frame
1½ year
Secondary Outcome Measure Information:
Title
Time to first symptomatic UTI after the intervention
Description
Symptoms and the need for medical treatment or hospitalisation
Time Frame
1½ year
Title
Quality of life by standard Questionnaires_ICIQ-LUT
Description
ICIQ-LUTSqol 08/04 questionnaire evaluating quality of life (QoL) in urinary incontinent patients (overall score with greater values indicating increased symptom severity)
Time Frame
1½ year
Title
Quality of life by standard Questionnaires_SF36
Description
SF-36 (scored so that a high score defines a more favorable health state)
Time Frame
1½ year
Title
EQ-5D-5L
Description
Questionnaire evaluating quality of life at 5 terms (mobility, self-care, usual activities, pain, discomfort and anxiety/depression)
Time Frame
1½ year
Title
CRF
Description
Case report form with respect to urinary/bladder symptoms, odour, perfomancestatus ect)
Time Frame
1½ year
Title
Hospitalization
Description
Hospital visit
Time Frame
1½ year
Title
Complications (bleeding, pain)
Description
Complications due to bladder lavage
Time Frame
1½ year
Title
Microbiological diagnostics: Etiology, resistance
Description
Measurements during treatment protocol
Time Frame
1½ year
Other Pre-specified Outcome Measures:
Title
Para-clinical findings: C reactive protein, leukocytes, Na, K, renal function (creatinine)
Description
Measurements during treatment protocol
Time Frame
1½ year
Title
Lower Urinary Tract Disease
Description
ICIQ-FLUTS LF or ICIQ-MLUTS LF questionnaire for detailed evaluation of female/male lower urinary tract symptoms and impact on quality of life (overall score with greater values indicating increased symptom severity)
Time Frame
1½ year
Title
Sexual function
Description
ICIQ-FLUTSsex or ICIQ-MLUTSsex evaluation of female/male sexual matters associated with their lower urinary tract symptoms and impact on quality of life (overall score with greater values indicating increased symptom severity)
Time Frame
1½ year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Diagnosed with recurrent cystitis including 2 times of rUTI within the last 6 months or 3 times in the last 12 months, where at least 2 cultures show the same bacteria.
Normal investigation for lower urinary tract diseases (LUTD) including voiding diary, symptom scores, flexible cystoscopy, voiding diagram and test for residual urine.
Failed previously treatments.
Patients with native bladder with both spontaneous voiding, the need for clean intermittent catheter (CIC) or indwelling catheter.
Patients with neurogenic and non-neurogenic bladder dysfunction.
Patients with urostomy, kidney transplantation or another complicated genesis.
Written consent.
Exclusion Criteria:
Malignancy in the urinary tract, kidney-, ureteral- or bladder stones, age < 18 years, pregnancy, breastfeeding. Patients in ongoing orally antibiotic treatment. Not able to speak or understand Danish.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Karin Andersen, MD
Phone
+45 21570468
Email
karin.andersen@rsyd.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Lars Lund, Prof.
Email
lars.lund@rsyd.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karin Andersen
Organizational Affiliation
University of Southern Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Odense university hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
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Bacterial Interference for Preventing Recurrent Urinary Tract Infection - New Ways of Treatment
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