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Mechanisms of Preventing Antibiotic-Associated Diarrhea and the Role for Probiotics (YOBIOTIC)

Primary Purpose

Antibiotic-associated Diarrhea

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet
BB-12
Control
Sponsored by
Georgetown University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Antibiotic-associated Diarrhea

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Has the ability to read, speak, and write in English
  2. Has refrigerator (for proper storage of the study yogurt)
  3. Has reliable telephone access
  4. Is between ages of 18-65 years
  5. Agree to refrain from eating yogurts, yogurt drinks, and other foods specified in the provided What Not to Eat list
  6. Agree to collect stool samples and participate in follow-up calls as specified

Exclusion Criteria:

  1. Diabetes or asthma that requires medication
  2. Allergy to strawberry
  3. Active diarrhea (three or more loose stools per day for two consecutive days)
  4. Any gastrointestinal (or digestive tract) medications, i.e. medicines for irritable bowel syndrome, gastroesophageal (acid) reflux disease, inflammatory bowel disease, etc.
  5. History of heart disease, including valvulopathies or cardiac surgery, any implantable device or prosthetic
  6. History of gastrointestinal surgery or disease
  7. Lactose intolerance that prevents participant from eating yogurt
  8. Allergy to milk-protein
  9. Allergy to any component of the product or the yogurt vehicle
  10. Allergy to penicillin or cephalosporin class antibiotics
  11. Allergy to any of the following medications: a) Penicillin; b) Erythromycin; c) Tetracycline; d) Trimethoprim; e) Ciprofloxacin
  12. Women who are breastfeeding, pregnant, or planning to become pregnant during the study

Sites / Locations

  • Georgetown University Department of Family Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control

BB-12

Arm Description

Yogurt without Bifidobacterium animalis subsp. lactis BB-12 (BB-12) and Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet

Bifidobacterium animalis subsp. lactis BB-12 (BB-12)-supplemented yogurt and Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet

Outcomes

Primary Outcome Measures

Level of Fecal Short-chain Fatty Acid (SCFA) Acetate
Level of fecal short-chain fatty acid acetate (SCFA) after administration of amoxicillin clavulanate

Secondary Outcome Measures

Level of Fecal SCFA Propionate
Level of fecal short-chain fatty acid propionate after administration of amoxicillin clavulanate
Level of Fecal SCFA Butyrate
Level of fecal short-chain fatty acid butyrate (μM) after administration of amoxicillin clavulanate

Full Information

First Posted
November 18, 2018
Last Updated
February 15, 2023
Sponsor
Georgetown University
Collaborators
National Center for Complementary and Integrative Health (NCCIH), University of Maryland, Baltimore
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1. Study Identification

Unique Protocol Identification Number
NCT03755765
Brief Title
Mechanisms of Preventing Antibiotic-Associated Diarrhea and the Role for Probiotics
Acronym
YOBIOTIC
Official Title
Exploratory Pilot Studies to Demonstrate Mechanisms of Preventing Antibiotic-Associated Diarrhea and the Role for Probiotics
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
July 23, 2019 (Actual)
Primary Completion Date
January 8, 2020 (Actual)
Study Completion Date
January 8, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Georgetown University
Collaborators
National Center for Complementary and Integrative Health (NCCIH), University of Maryland, Baltimore

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The focus of the study is to better understand the mechanisms causing antibiotic-associated diarrhea (AAD) and how probiotics may prevent some of the iatrogenic effects of antibiotic medications. One of the most common indications for probiotics is for prevention of antibiotic-associated diarrhea. Clinically, different probiotic strains have demonstrated the ability to prevent AAD; however, the mechanism of action behind this effect has not been elucidated. Data from several studies suggest that antibiotic-induced disruption of commensal bacteria in the colon results in a significant (up to 50%) reduction in short chain fatty acid (SCFA) production and a concomitant reduction in Na-dependent fluid absorption resulting in AAD. Probiotics have been shown to ameliorate a variety of gastrointestinal disease states and thus, the study investigators hypothesize that administration of a probiotic yogurt will protect against the development of AAD.
Detailed Description
Probiotics are live microorganisms that, when administered in adequate amounts, confer a health benefit on the host. One of the most common indications for probiotic treatment is the prevention of antibiotic-associated diarrhea (AAD). Unfortunately, the efficacy of many probiotic products used for AAD is not supported by rigorous independent research, and non-evidence-based clinical usage is common. Data from several studies are consistent with the notion that antibiotic-induced disruption of commensal bacteria in the colon results in a significant reduction of short chain fatty acid (SCFA) production and a concomitant reduction in Na-dependent fluid absorption resulting in AAD. The probiotic strain being studied, Bifidobacterium animalis subsp. lactis BB-12 (BB-12), has been shown to ameliorate a variety of gastrointestinal disease states and is known to produce acetate at concentrations up to 50 mM in vitro. Thus, the investigators hypothesize that administration of BB-12 at the same time as antibiotic consumption will protect against the development of AAD through its ability to generate acetate directly, and also increase other SCFAs through cross-feeding of certain bacteria in the Firmicutes phylum such Clostridium, Eubacterium and Roseburia, which use acetate to produce butyrate. The primary aim of the R61 phase (N=60) is to determine the ability of BB-12 to impact antibiotic-induced reduction in SCFA as reflected by the levels of acetate, the most abundant primary colonic SCFA. The primary hypothesis is that antibiotics will result in a reduction in fecal SCFA, but BB-12 supplementation will protect against antibiotic-induced SCFA reduction and/or be associated with a more rapid return to baseline SCFA levels as compared to controls. Antibiotics also result in a decrease in total microbial counts and diversity in the gut microbiota, disrupting the homeostasis of the gut ecosystem and allowing colonization by pathogens. The secondary aim will be to determine the ability of BB-12 to impact antibiotic-induced disruption of the gut microbiota with 16S (16 Svedberg) ribosomal ribonucleic acid (rRNA) profiling. The secondary hypothesis is that antibiotics will result in a decrease in the overall number and diversity of bacterial species present in the fecal microbiota, and further BB-12 supplementation will protect against antibiotic-induced shifts in the microbiota and/or will be associated with a more rapid return to a baseline microbiota composition as compared to controls. The long-term goal is to determine the impact of BB-12 on a variety of gastrointestinal disease states and ages, through high-level independent research. This mechanism elucidation is important for directing future translational and effectiveness research.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Antibiotic-associated Diarrhea

7. Study Design

Primary Purpose
Other
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
66 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Yogurt without Bifidobacterium animalis subsp. lactis BB-12 (BB-12) and Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet
Arm Title
BB-12
Arm Type
Experimental
Arm Description
Bifidobacterium animalis subsp. lactis BB-12 (BB-12)-supplemented yogurt and Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet
Intervention Type
Drug
Intervention Name(s)
Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet
Other Intervention Name(s)
Augmentin
Intervention Description
Amoxicillin-Clavulanate 875 Mg-125 Mg Oral Tablet
Intervention Type
Biological
Intervention Name(s)
BB-12
Intervention Description
Bifidobacterium animalis subsp. lactis BB-12-supplemented yogurt
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Yogurt without Bifidobacterium animalis subsp. lactis BB-12 (BB-12)
Primary Outcome Measure Information:
Title
Level of Fecal Short-chain Fatty Acid (SCFA) Acetate
Description
Level of fecal short-chain fatty acid acetate (SCFA) after administration of amoxicillin clavulanate
Time Frame
day 0 (post run-in), 7, 14, 21, 30
Secondary Outcome Measure Information:
Title
Level of Fecal SCFA Propionate
Description
Level of fecal short-chain fatty acid propionate after administration of amoxicillin clavulanate
Time Frame
day 0 (post run-in), 7, 14, 21, 30
Title
Level of Fecal SCFA Butyrate
Description
Level of fecal short-chain fatty acid butyrate (μM) after administration of amoxicillin clavulanate
Time Frame
day 0 (post run-in), 7, 14, 21, 30
Other Pre-specified Outcome Measures:
Title
Change in Community Diversity (Shannon Diversity Index) From Pre run-in Baseline
Description
The Shannon diversity metric is a measure of community diversity and takes into account species richness (number of distinct taxa) and the relative abundance of each taxon. The Shannon diversity index was calculated for samples at each time point from subjects receiving control or BB-12 yogurt. The first of two baseline samples was collected from each subject at the time of enrollment (pre run-in) before a 30-day run-in period in which the consumption of dietary probiotics was stopped. A higher index indicates more diversity and a lower index indicates less diversity.
Time Frame
day 0 (pre run-in), 7, 14, 21, 30
Title
Change in Community Diversity (Shannon Diversity Index) From Post run-in Baseline
Description
The Shannon diversity metric is a measure of community diversity and takes into account species richness (number of distinct taxa) and the relative abundance of each taxon. The Shannon diversity index was calculated for samples at each time point from subjects receiving control or BB-12 yogurt. The second baseline sample was collected from each subject after a 30-day run-in period in which the consumption of dietary probiotics was stopped (post run-in). A higher index indicates more diversity and a lower index indicates less diversity.
Time Frame
day 0 (post run-in), 7, 14, 21, 30
Title
Bray-Curtis Dissimilarity
Description
Community divergence over time with respect to the baseline sample (post run-in, day 0)
Time Frame
day 0, 7, 14, 21, 30
Title
Change in Diarrhea/Stool Frequency
Description
Change in diarrhea/stool frequency from baseline
Time Frame
day 7, 14, 21, 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Has the ability to read, speak, and write in English Has refrigerator (for proper storage of the study yogurt) Has reliable telephone access Is between ages of 18-65 years Agree to refrain from eating yogurts, yogurt drinks, and other foods specified in the provided What Not to Eat list Agree to collect stool samples and participate in follow-up calls as specified Exclusion Criteria: Diabetes or asthma that requires medication Allergy to strawberry Active diarrhea (three or more loose stools per day for two consecutive days) Any gastrointestinal (or digestive tract) medications, i.e. medicines for irritable bowel syndrome, gastroesophageal (acid) reflux disease, inflammatory bowel disease, etc. History of heart disease, including valvulopathies or cardiac surgery, any implantable device or prosthetic History of gastrointestinal surgery or disease Lactose intolerance that prevents participant from eating yogurt Allergy to milk-protein Allergy to any component of the product or the yogurt vehicle Allergy to penicillin or cephalosporin class antibiotics Allergy to any of the following medications: a) Penicillin; b) Erythromycin; c) Tetracycline; d) Trimethoprim; e) Ciprofloxacin Women who are breastfeeding, pregnant, or planning to become pregnant during the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Merenstein, MD
Organizational Affiliation
Georgetown University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Claire Fraser, PhD
Organizational Affiliation
University of Maryland, Baltimore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Georgetown University Department of Family Medicine
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20007
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
34444974
Citation
Merenstein D, Fraser CM, Roberts RF, Liu T, Grant-Beurmann S, Tan TP, Smith KH, Cronin T, Martin OA, Sanders ME, Lucan SC, Kane MA. Bifidobacterium animalis subsp. lactis BB-12 Protects against Antibiotic-Induced Functional and Compositional Changes in Human Fecal Microbiome. Nutrients. 2021 Aug 17;13(8):2814. doi: 10.3390/nu13082814.
Results Reference
result

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Mechanisms of Preventing Antibiotic-Associated Diarrhea and the Role for Probiotics

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