Probiotics Effect on the Female Urinary Microbiome ProFUM Trial (Probiotics Effect on the Female Urinary Microbiome)

NCT ID: NCT03250208

Last Updated: 2019-02-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 8 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-09-01
• Study Completion Date: 2018-07-31

Brief Summary

The study will enroll healthy pre-menopausal female volunteers in the community. These subjects will act as their own controls. The subjects will collect voided urine and peri-urethral swab specimens daily for several months. They will also be asked to collect vaginal and peri-rectal swab specimens at various time points. Subjects will document various lifestyle variables daily. During the middle of the study, subjects will be randomized to probiotic vs placebo. Using bacterial culture and 16S rRNA gene sequencing, the study will measure the bacterial populations of several anatomic sites longitudinally: voided urine, peri-urethra, vagina, and peri-rectal. The study hypothesizes that oral probiotic usage will alter the bacterial populations and ratio of Lactobacillus to E. coli within each of these sites. Additionally, the study hypothesizes that the changes within each site will occur first in the rectum (i.e. GI tract), followed by the vagina, and then the urethra and bladder.

Using the prospective design of daily sampling and lifestyle variable documentation, the study may be able to identify possible influences on microbiome stability within the sampled sites. The lifestyle variables recorded include: diet, medication usage, menstruation, sexual activity, and alcohol consumption.

This pilot study will establish the variance of the outcome variables among healthy women and confirm the emergence of the probiotic with the recommended dose. With this information, future researchers will be able to calculate the power needed for a larger randomized trial. This trial would also randomize patients who may be at risk for a UTI to receive a probiotic vs placebo. The primary outcome measurement will be the change in the ratio of Lactobacillus to E. coli. As a secondary aim, the study will evaluate the incidence of UTI in the patients.

Detailed Description

In this study, the primary aim is to identify the change in the Lactobacillus E. coli ratio within the lower urinary tract, the vagina, and the peri-rectal area in response to an oral probiotic as well as to evaluate the stability of these changes following cessation of an oral probiotic. Voided urine and peri-urethral, vaginal, and peri-rectal swab samples will be analyzed for their Lactobacillus E. coli ratio using bacterial culture as well as 16S ribosomal RNA gene sequencing. The study will compare the ratios present before, during, and after oral probiotic usage. The study will also compare the change in ratios between subjects taking the oral probiotic and those taking an oral placebo.

A secondary aim is to identify the normal daily changes (i.e. stability) in the bacterial populations within the voided urine, including whether host intrinsic (e.g. diet, hygiene, and sexual activity) and extrinsic (e.g. menstruation) factors affect the stability of bacterial populations. The bacterial populations defining the voided urine samples will be correlated to various daily subject-reported lifestyle variables. These include diet, hygiene, sexual activity, medication usage, alcohol usage, menstruation, and urinary-related symptoms. These lifestyle variables will be recorded each day for the entire duration of the study.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: QUADRUPLE

Study Groups

Control Group

Participants randomized to this group will take two placebo capsules daily during days 21-60.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Participants randomized to the control group will receive a placebo containing no active ingredients

Intervention group

The intervention in this study is a probiotic. Participants randomized to this group will take two capsules of a probiotic daily during days 21-60

Group Type: EXPERIMENTAL

Probiotic

Intervention Type: DIETARY_SUPPLEMENT

Participants randomized to the intervention group will receive Women's Fem Dophilus ® by Jarrow Formulas.

Interventions

Probiotic

Participants randomized to the intervention group will receive Women's Fem Dophilus ® by Jarrow Formulas.

Intervention Type: DIETARY_SUPPLEMENT

Placebo

Participants randomized to the control group will receive a placebo containing no active ingredients

Intervention Type: OTHER

Other Intervention Names

Fem Dophilus; Inactive substance

Eligibility Criteria

Inclusion Criteria

• Pre-menopausal healthy women in the community (As defined by presence of menses at least once in the last 12 months).
• Age 18 years or older.
• Agreement to collect daily samples (varying combinations of voided, periurethral, and perianal swabs) for 3 months and bring the samples to Loyola University Medical Center
• Agree to record and return a daily lifestyle diary
• Understand and agree to taking daily oral probiotic or placebo while being blinded
• Able to read and speak English
• Able to obtain clean-catch urine

Exclusion Criteria

• Non-English speaking women
• Allergy or contraindication to the probiotic used in this study
• Prior participation in the study
• Currently pregnant or lactating or planning a pregnancy within 6 months of consenting to participate in the study
• Inability to obtain a 'clean catch' urine sample
• Subjects with an indwelling catheter
• Males are excluded from participation
• Women planning time away for more than 7 days following consent to participate in the study

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Loyola University

OTHER

Sponsor Role: lead

Responsible Party

Elizabeth Mueller

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Elizabeth Mueller, MD

Role: PRINCIPAL_INVESTIGATOR

Loyola University Health System

Locations

Loyola University Medical Center

Maywood, Illinois, United States

Countries

United States

References

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Other Identifiers

209830

Identifier Type: -

Identifier Source: org_study_id