- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00717600
Bacteriuria Eradication Through Probiotics (BERP)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In children with spina bifida and neurogenic bladder dysfunction, the need for intermittent bladder catheterization increases the risk of bacteriuria. In many patients, this leads to a clinically significant urinary tract infection (UTI). Many of these children are placed on long term, low dose antibiotic suppression to prevent recurrent urinary infection. Unfortunately, bacteriuria often persists despite daily antibiotic therapy, and breakthrough urinary tract infections are common. Furthermore, this approach carries the potential for deleterious side effects, and may promote the development of antibiotic-resistant bacteria.
Urinary tract infection in girls occurs when virulent bacteria migrate from the rectum and colonize the vagina and peri-urethral mucosa, thus gaining access to the bladder. In girls with spina bifida, access to the bladder is greatly facilitated by catheter passage. Antibiotic prophylaxis relies on maintaining a low dose of antibiotic in the urinary stream, which decreases peri-urethral colonization, and prevents proliferation of bacteria after they gain access to the bladder. An alternative approach to daily antibiotic prophylaxis is to decrease the risk of urinary colonization with virulent bacteria by supplementing the normal bacteria flora with non-infection causing strains of bacteria.
Probiotics are dietary supplements containing potentially beneficial bacterial strains such as Lactobacillus. The safety of oral administration of probiotics has been demonstrated in several studies over the last 30 years. Studies using L. rhamnosus GG, a probiotic introduced in the late 1980s to alleviate diarrhea, have shown promising results when used for UTI prevention. In one study, researchers found that the subjects consuming Lactobacillus GG drinks had fewer episodes of UTI compared to those women not receiving probiotics. A placebo-controlled study in premature infants also used L. rhamnosus GG in an attempt to prevent UTI. The number of urinary infections was reduced but statistically the difference was not significant. Finally, a recent randomized clinical trial demonstrated that the rate of UTI in patients taking prophylactic antibiotics was similar to that of patients taking Lactobacillus acidophilus alone. The efficacy of probiotic usage in the spina bifida population has not been reported.
Our objective is to determine whether over the course of 3 months, probiotics can reduce preexisting or new bacteriuria in girls with spina bifida who perform clean intermittent catheterization for bladder emptying. We will also attempt to ascertain whether changes in bacteriuria are associated with vaginal colonization by the administered probiotics.
Study Type
Enrollment (Anticipated)
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- Texas Children's Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Eligible subjects are girls (age 3 months to 18 years) with spina bifida as a sole urologic diagnosis
- perform clean intermittent catheterization because of neurogenic bladder.
- Secondary vesicoureteral reflux is permissible.
- Patients with appendicovesicostomies and no other forms of urinary diversion are permitted.
Exclusion Criteria:
- Patients will be excluded if they are taking antibiotics
- immunosuppressed, i.e., transplant recipients or children with congenital immunodeficiencies
- poorly controlled diabetes
- untreated HIV infection
- immunosuppression from corticosteroids
- malnutrition
- pregnancy
- chronic indwelling catheters in the bladder
- any urinary diversion or bladder augmentation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1
Oral probiotics
|
2x10^9 cfu of Lactobacillus reuteri RC-14 and Lactobacillus rhamnosus GR-1 administered daily via a single orally ingested freeze-dried capsule.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
bacteriuria
Time Frame: 3 months
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
urinary tract infections
Time Frame: 3 months
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eric A Jones, M.D., Texas Children's Hospital, Baylor College of Medicine
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-21679
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Bacteriuria
-
Military Institute of Medicine, PolandUnknownAsymptomatic Bacteriuria | Antimicrobial ProphylaxisPoland
-
Jorge Andres Ramos CastanedaUnknownAsymptomatic Bacteriuria | Antibiotic ProphylaxisColombia
-
Mount Sinai Hospital, CanadaCompletedUrinary Tract Infections | Asymptomatic BacteriuriaCanada
-
University of California, IrvineCompletedAsymptomatic BacteriuriaUnited States
-
Abington Memorial HospitalUnknownPostoperative BacteriuriaUnited States
-
Centenario Hospital Miguel HidalgoCompletedKidney Transplant Infection | Asymptomatic BacteriuriaMexico
-
NovaBay Pharmaceuticals, Inc.CompletedAsymptomatic BacteriuriaUnited States
-
Kendall Healthcare Group, Ltd.CompletedAsymptomatic Bacteriuria | Asymptomatic PyuriaUnited States
-
Saint Joseph Mercy Health SystemTerminatedBacteriuria (Asymptomatic) in PregnancyUnited States
-
Aljazeera HospitalKasr El Aini HospitalUnknown
Clinical Trials on Lactobacillus reuteri RC-14 and Lactobacillus rhamnosus GR-1
-
Azienda Ospedaliero, Universitaria PisanaCompleted
-
Oswaldo Cruz FoundationMinistry of Health, BrazilTerminatedSepsis | Premature Birth | Bronchopulmonary Dysplasia | Bacterial Vaginosis | Periventricular LeukomalaciaBrazil
-
National Institute for Medical Research, TanzaniaErasmus Medical Center; Lawson Health Research Institute; University of Western... and other collaboratorsUnknownHIV Infections | Diarrhea | Bacterial VaginosisTanzania
-
Glac Biotech Co., LtdActive, not recruitingAllergic RhinitisTaiwan
-
Baylor College of MedicineShriners Hospitals for ChildrenWithdrawn
-
Lawson Health Research InstituteUniversity of Western Ontario, Canada; St. Joseph's Health Care LondonCompleted
-
Western University, CanadaCompletedBacterial Vaginosis | Vulvovaginal CandidiasisRwanda
-
Peking University Shenzhen HospitalBGI, ChinaCompleted
-
Lawson Health Research InstituteOntario Neurotrauma FoundationTerminatedUrinary Tract Infections | Spinal Cord InjuryCanada
-
Faith MediplexChr Hansen; UrexBiotechUnknownVaginal CandidiasisNigeria