Probiotics and Multi-Drug Resistant Urinary Tract Infection
Primary Purpose
Urinary Tract Infections, Recurrent UTI, Antibiotic Resistant Infection
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bifidobacterium infantis
Placebo
Antibiotics
Sponsored by
About this trial
This is an interventional treatment trial for Urinary Tract Infections focused on measuring Probiotics, multi-drug resistant UTI, recurrent UTI
Eligibility Criteria
Inclusion Criteria:
- Female, age 18-90
- Ability to void spontaneously
- Suffers from recurrent multi-drug resistant or extensively drug resistant urinary tract infections caused by E.coli, Klebsiella, Enterococcus, Citrobacter, Proteus, Enterobacter, Serratia and Providencia.
Exclusion Criteria:
- Has staghorn renal calculi, chronic hydronephrosis, intermittent catherization, indwelling urinary catheters, urinary diversions, end stage renal disease on hemodialysis, transplantation, HIV, cirrhosis, pancreatitis, allergy to soy or milk/milk proteins or lactose intolerance
- Pregnant or breastfeeding
- Currently taking probiotics. 4 week washout.
Sites / Locations
- Ochsner Health System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Probiotic + Antibiotic
Placebo + Antibiotic
Arm Description
50 subjects to receive probiotic supplement once daily for 6 months in capsule form, in addition to standard antibiotic regimen for treatment of UTI.
50 subjects to receive placebo once daily for 6 months in capsule form, in addition to antibiotic regimen for treatment of UTI.
Outcomes
Primary Outcome Measures
Change in Resistance Pattern
The change in the quantity of antibiotics reported to be resistant per organism per culture per patient.
Bacterial isolate genomic characteristics
genomic sequencing of bacterial isolates to determine genetic identity
Secondary Outcome Measures
UTI reduction
The quantity of reduction of all urinary tract infections (UTI) in treatment arm vs. placebo from baseline.
Antibiotics Quantity
The quantity of antibiotics prescribed in treatment arm vs. placebo.
Healthcare visit
The quantity of ER visits/urgent care visits/hospitalizations/outpatient clinic visits in treatment arm vs. placebo.
Length of time for change in resistance
The amount of time it takes to note changes in antibiotic sensitivity patterns while on the treatment arm.
Sensitivity pattern post-probiotic therapy
The change in the quantity of antibiotics reported to be resistant per organism
Full Information
NCT ID
NCT03644966
First Posted
August 6, 2018
Last Updated
April 10, 2023
Sponsor
Ochsner Health System
Collaborators
Procter and Gamble
1. Study Identification
Unique Protocol Identification Number
NCT03644966
Brief Title
Probiotics and Multi-Drug Resistant Urinary Tract Infection
Official Title
Probiotic and Effects on Multi-Drug Resistant Urinary Tract Infection
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
July 5, 2018 (Actual)
Primary Completion Date
December 15, 2022 (Actual)
Study Completion Date
December 15, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ochsner Health System
Collaborators
Procter and Gamble
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
This pilot study is a single-site randomized, double blinded placebo-controlled in females with recurrent multi-drug resistant (MDR) urinary tract infections(UTI). Our study hypothesizes that a novel probiotic strain improves antibiotic sensitivity patterns in these former MDR UTIs.
Detailed Description
The aims of this study are (1) to evaluate the effects of six months of probiotic therapy in addition to standard of care in changing sensitivity patterns of MDR bacteria causing recurrent UTI, (2) analyze the genetic composition of MDR bacterial isolates causing recurrent UTI before and after administration of probiotic vs. placebo, with standard of care antibiotics.
Study subjects will be asked to take a either a probiotic supplement or placebo at a dose of 1 caplet per day for 24 weeks in addition to antibiotic regimen. Subjects will be followed for 12 months. The outcome measure is the percent of probiotic ingestors vs placebo ingestors who experience a change in antibiotic susceptibility over this time period. The secondary outcome measure is the evaluation of genetic composition of bacteria recurring after probiotic vs. placebo administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infections, Recurrent UTI, Antibiotic Resistant Infection
Keywords
Probiotics, multi-drug resistant UTI, recurrent UTI
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Probiotic + Antibiotic
Arm Type
Experimental
Arm Description
50 subjects to receive probiotic supplement once daily for 6 months in capsule form, in addition to standard antibiotic regimen for treatment of UTI.
Arm Title
Placebo + Antibiotic
Arm Type
Active Comparator
Arm Description
50 subjects to receive placebo once daily for 6 months in capsule form, in addition to antibiotic regimen for treatment of UTI.
Intervention Type
Dietary Supplement
Intervention Name(s)
Bifidobacterium infantis
Other Intervention Name(s)
Align
Intervention Description
Probiotics
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
Placebo (for Probiotic)
Intervention Description
Sugar pill manufactured to mimic probiotic tablet
Intervention Type
Drug
Intervention Name(s)
Antibiotics
Intervention Description
Per Infectious Disease Society guidelines for Antimicrobial treatment of uncomplicated cystitis and pyelonephritis in women
Primary Outcome Measure Information:
Title
Change in Resistance Pattern
Description
The change in the quantity of antibiotics reported to be resistant per organism per culture per patient.
Time Frame
6-8 weeks after initial dose
Title
Bacterial isolate genomic characteristics
Description
genomic sequencing of bacterial isolates to determine genetic identity
Time Frame
12 months after initial dose
Secondary Outcome Measure Information:
Title
UTI reduction
Description
The quantity of reduction of all urinary tract infections (UTI) in treatment arm vs. placebo from baseline.
Time Frame
12 months after initial dose
Title
Antibiotics Quantity
Description
The quantity of antibiotics prescribed in treatment arm vs. placebo.
Time Frame
12 months after initial dose
Title
Healthcare visit
Description
The quantity of ER visits/urgent care visits/hospitalizations/outpatient clinic visits in treatment arm vs. placebo.
Time Frame
12 months after initial dose
Title
Length of time for change in resistance
Description
The amount of time it takes to note changes in antibiotic sensitivity patterns while on the treatment arm.
Time Frame
12 months after initial dose
Title
Sensitivity pattern post-probiotic therapy
Description
The change in the quantity of antibiotics reported to be resistant per organism
Time Frame
12 months after initial dose
10. Eligibility
Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female, age 18-90
Ability to void spontaneously
Suffers from recurrent multi-drug resistant or extensively drug resistant urinary tract infections caused by E.coli, Klebsiella, Enterococcus, Citrobacter, Proteus, Enterobacter, Serratia and Providencia.
Exclusion Criteria:
Has staghorn renal calculi, chronic hydronephrosis, intermittent catherization, indwelling urinary catheters, urinary diversions, end stage renal disease on hemodialysis, transplantation, HIV, cirrhosis, pancreatitis, allergy to soy or milk/milk proteins or lactose intolerance
Pregnant or breastfeeding
Currently taking probiotics. 4 week washout.
Facility Information:
Facility Name
Ochsner Health System
City
Jefferson
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
24847423
Citation
Naderi A, Kasra-Kermanshahi R, Gharavi S, Imani Fooladi AA, Abdollahpour Alitappeh M, Saffarian P. Study of antagonistic effects of Lactobacillus strains as probiotics on multi drug resistant (MDR) bacteria isolated from urinary tract infections (UTIs). Iran J Basic Med Sci. 2014 Mar;17(3):201-8.
Results Reference
background
PubMed Identifier
26695595
Citation
Schwenger EM, Tejani AM, Loewen PS. Probiotics for preventing urinary tract infections in adults and children. Cochrane Database Syst Rev. 2015 Dec 23;2015(12):CD008772. doi: 10.1002/14651858.CD008772.pub2.
Results Reference
background
PubMed Identifier
28480273
Citation
Simmering JE, Tang F, Cavanaugh JE, Polgreen LA, Polgreen PM. The Increase in Hospitalizations for Urinary Tract Infections and the Associated Costs in the United States, 1998-2011. Open Forum Infect Dis. 2017 Feb 24;4(1):ofw281. doi: 10.1093/ofid/ofw281. eCollection 2017 Winter.
Results Reference
background
PubMed Identifier
29170359
Citation
Barclay J, Veeratterapillay R, Harding C. Non-antibiotic options for recurrent urinary tract infections in women. BMJ. 2017 Nov 23;359:j5193. doi: 10.1136/bmj.j5193. No abstract available.
Results Reference
background
PubMed Identifier
29487733
Citation
Vahedi-Shahandashti R, Kasra-Kermanshahi R, Shokouhfard M, Ghadam P, Feizabadi MM, Teimourian S. Antagonistic activities of some probiotic lactobacilli culture supernatant on Serratia marcescens swarming motility and antibiotic resistance. Iran J Microbiol. 2017 Dec;9(6):348-355.
Results Reference
background
PubMed Identifier
26955289
Citation
Lau CS, Chamberlain RS. Probiotics are effective at preventing Clostridium difficile-associated diarrhea: a systematic review and meta-analysis. Int J Gen Med. 2016 Feb 22;9:27-37. doi: 10.2147/IJGM.S98280. eCollection 2016.
Results Reference
background
PubMed Identifier
9125655
Citation
Favier C, Neut C, Mizon C, Cortot A, Colombel JF, Mizon J. Fecal beta-D-galactosidase production and Bifidobacteria are decreased in Crohn's disease. Dig Dis Sci. 1997 Apr;42(4):817-22. doi: 10.1023/a:1018876400528.
Results Reference
background
PubMed Identifier
21292654
Citation
Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG, Moran GJ, Nicolle LE, Raz R, Schaeffer AJ, Soper DE; Infectious Diseases Society of America; European Society for Microbiology and Infectious Diseases. International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. Clin Infect Dis. 2011 Mar 1;52(5):e103-20. doi: 10.1093/cid/ciq257.
Results Reference
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Probiotics and Multi-Drug Resistant Urinary Tract Infection
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