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| ID | Type | Description | Link |
|---|---|---|---|
| OMB 4040-0001 | Other Identifier | University of Wisconsin, Madison |
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| Name | Class |
|---|---|
| University of Wisconsin, Madison | OTHER |
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The investigators have two hypotheses: (1) The probiotic L. rhamnosus HN001, when compared to placebo, will reduce S. aureus nasal colonization when taken for four weeks. (2) The probiotic L. rhamnosus HN001, when compared to placebo, will reduce S. aureus gastrointestinal colonization when taken for four weeks.
Reducing infections caused by S. aureus is essential. The knowledge that colonization at a few key body sites such as the nose and the gastrointestinal tract is a prerequisite for infection2 ,3 offers an opportunity for therapeutic intervention. Thirty percent of the population has nasal colonization with S. aureus. In the last few years, decolonization agents such as mupirocin topical ointment and oral antibiotics such as doxycycline and rifampin have been studied for their utility in reducing colonization. However, these options have limitations in that recolonization is common, the impact of these interventions on multiple sites of colonization has not been assessed and resistance develops frequently to any of these, especially the oral antibiotics. Resistance in S. aureus has been designated a public health crisis. Methicillin-resistant S. aureus (MRSA) now accounts for 60% of all S. aureus infections. As an example of the growing crisis in S. aureus resistance, it should be noted that the number of MRSA infections rose from 2000 in 1993 to 368,000 in 2005. MRSA infections pose an even greater health and economic burden on the population than those caused by methicillin-sensitive S. aureus.4-8 S. aureus and MRSA infection trends in the VA health system mirror national trends5 and are associated with considerable morbidity and mortality in Veterans. A treatment that reduces S. aureus and MRSA colonization, without a risk of promoting antibiotic resistance could represent a breakthrough in decolonization therapy. Probiotics may be one such treatment option.
Probiotics are live microorganisms that are available over the counter, widely used as dietary supplements or nutritional foods and represent a low-cost, well tolerated, safe, non-antibiotic based strategy that may have efficacy for decolonization without the attendant risks of promoting antimicrobial resistance.9 Certain probiotics, including Lactobacillus rhamnosus HN001, have demonstrated ability to stimulate systemic immune functions, possibly enhancing the body's ability to eradicate S. aureus in the gastrointestinal tract and at sites remote from the gastrointestinal tract such as the nose.10 ,11 The long-term goal of this research is to identify and test novel interventions for reducing infections caused by resistant bacteria. The investigators propose a Phase II randomized, double-blind, placebo-controlled clinical trial in Veterans to evaluate the efficacy of an oral probiotic, Lactobacillus rhamnosus HN001, for reducing S. aureus colonization. This study will produce data, methods, and tools that have widespread relevance and portability, with the potential to reduce healthcare-associated infections.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm 1: Probiotic | Experimental | subjects will be given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks |
|
| Arm 2: Placebo | Placebo Comparator | Placebo identical to the active product will be given |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lactobacillus rhamnosus HN001 | Dietary Supplement | Subjects will be given a pill formulation of a probiotic L. rhamnosus HN001 to be taken once a day, at a dose of 1 x 10^10 organisms |
| Measure | Description | Time Frame |
|---|---|---|
| Oral L. Rhamnosus HN001 Therapy Compared to Placebo on Gastrointestinal and Extra-gastrointestinal Colonization of S. Aureus. | Participants in the final outcome may be colonized at both GI and Extra-GI sites, thus the total numbers from the outcome cells can be greater than the overall number of participants analyzed. | 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Oral L. Rhamnosus HN001 Therapy Compared With Placebo on Phagocytic Functioning of Polymorphonuclear (PMN) and Monocyte Cells | This outcome is the mean difference in the % of granulocytes that phagocytized E. coli, from blood samples taken at the beginning and end of the trial. Percent of granulocytes phagocytizing E. coli at baseline is subtracted by percent of granulocytes phagocytizing E. coli at the end of the trial. The mean and standard error are calculated and reported for each study arm. This result |
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Inclusion Criteria:
Exclusion Criteria:
Uncontrolled psychiatric illness
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| Name | Affiliation | Role |
|---|---|---|
| Nasia Safdar, MD PhD | William S. Middleton Memorial Veterans Hospital, Madison, WI | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| William S. Middleton Memorial Veterans Hospital, Madison, WI | Madison | Wisconsin | 53705 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29540160 | Derived | Eggers S, Barker AK, Valentine S, Hess T, Duster M, Safdar N. Effect of Lactobacillus rhamnosus HN001 on carriage of Staphylococcus aureus: results of the impact of probiotics for reducing infections in veterans (IMPROVE) study. BMC Infect Dis. 2018 Mar 14;18(1):129. doi: 10.1186/s12879-018-3028-6. | |
| 27836508 | Derived |
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| ID | Title | Description |
|---|---|---|
| FG000 | Arm 1a: Extra-GI Probiotic | Subjects with Extra-GI colonization at initial screening who were randomized to probiotic treatment. Extra-GI colonization was defined as a positive PCR result for S. aureus from any swab of the nares, axillae or wound, with no positive result from swabs of the oropharynx, or peri-rectum. Subjects were given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks. |
| FG001 | Arm 2a: Extra-GI Placebo | Subjects with Extra-GI colonization at initial screening who were randomized to placebo treatment. Extra-GI colonization was defined as a positive PCR result for S. aureus from any swab of the nares, axillae or wound, with no positive result from swabs of the oropharynx, or peri-rectum. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. |
| FG002 | Arm 1b: GI Probiotic | Subjects with GI colonization at initial screening who were randomized to probiotic treatment. GI colonization was defined as a positive PCR result for S. aureus from any swab of the oropharynx, or peri-rectum. Subjects were given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks |
| FG003 | Arm 2b: GI Placebo | Subjects with GI colonization at initial screening who were randomized to placebo treatment. GI colonization was defined as a positive PCR result for S. aureus from any swab of the oropharynx, or peri-rectum. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Arm 1: Probiotic | Subjects were given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks Lactobacillus rhamnosus HN001: Subjects will be given a pill formulation of a probiotic L. rhamnosus HN001 to be taken once a day, at a dose of 1 x 10^10 organisms |
| BG001 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Oral L. Rhamnosus HN001 Therapy Compared to Placebo on Gastrointestinal and Extra-gastrointestinal Colonization of S. Aureus. | Participants in the final outcome may be colonized at both GI and Extra-GI sites, thus the total numbers from the outcome cells can be greater than the overall number of participants analyzed. | Posted | Count of Participants | Participants | 4 weeks |
|
4 weeks
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Arm 1: Extra-GI Probiotic | Subjects with Extra-GI colonization at initial screening who were randomized to probiotic treatment. Subjects were given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks Lactobacillus rhamnosus HN001: Subjects will be given a pill formulation of a probiotic L. rhamnosus HN001 to be taken once a day, at a dose of 1 x 10^10 organisms |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Cardiovascular event | Cardiac disorders |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Fever | General disorders |
|
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Nasia Sardar | William S. Middleton Memorial Veterans Affairs Medical Center | 608-256-1901 | 17800 | nasia.safdar@va.gov |
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| ID | Term |
|---|---|
| D007239 | Infections |
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| ID | Term |
|---|---|
| D000073893 | Sugars |
| ID | Term |
|---|---|
| D002241 | Carbohydrates |
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| sugar pill (placebo) | Dietary Supplement | Placebo identical to the active product will be given |
|
| 4 weeks |
| Oral L. Rhamnosus HN001 Therapy Compared With Placebo on Phagocytic Functioning of Polymorphonuclear (PMN) and Monocyte Cells | This outcome is the mean difference in the % of monocytes that phagocytized E. coli, from blood samples taken at the beginning and end of the trial. Percent of monocytes phagocytizing E. coli at baseline is subtracted by percent of monocytes phagocytizing E. coli at the end of the trial. The mean and standard error are calculated and reported for each study arm. | 4 weeks |
| Eggers S, Barker A, Valentine S, Hess T, Duster M, Safdar N. Impact of Probiotics for Reducing Infections in Veterans (IMPROVE): Study protocol for a double-blind, randomized controlled trial to reduce carriage of Staphylococcus aureus. Contemp Clin Trials. 2017 Jan;52:39-45. doi: 10.1016/j.cct.2016.11.004. Epub 2016 Nov 9. |
| Arm 2: Placebo |
Placebo composed of identical inactive components to the active product, to be taken once daily for 4 weeks. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. |
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| OG001 |
| Arm 2a: Extra-GI Placebo |
Subjects with Extra-GI colonization at initial screening who were randomized to placebo treatment. Extra-GI colonization was defined as a positive PCR result for S. aureus from any swab of the nares, axillae or wound, with no positive result from swabs of the oropharynx, or peri-rectum. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. |
| OG002 | Arm 1b: GI Probiotic | Subjects with GI colonization at initial screening who were randomized to probiotic treatment. GI colonization was defined as a positive PCR result for S. aureus from any swab of the oropharynx, or peri-rectum. Subjects were given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks |
| OG003 | Arm 2b: GI Placebo | Subjects with GI colonization at initial screening who were randomized to placebo treatment. GI colonization was defined as a positive PCR result for S. aureus from any swab of the oropharynx, or peri-rectum. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. |
|
|
| Secondary | Oral L. Rhamnosus HN001 Therapy Compared With Placebo on Phagocytic Functioning of Polymorphonuclear (PMN) and Monocyte Cells | This outcome is the mean difference in the % of granulocytes that phagocytized E. coli, from blood samples taken at the beginning and end of the trial. Percent of granulocytes phagocytizing E. coli at baseline is subtracted by percent of granulocytes phagocytizing E. coli at the end of the trial. The mean and standard error are calculated and reported for each study arm. This result | Some participants were excluded from this analysis due to lack of sample collection, or unusable results because tests did not meet acceptability criteria. | Posted | Mean | Standard Error | Difference in % POS of Granulocytes | 4 weeks |
|
|
|
| Secondary | Oral L. Rhamnosus HN001 Therapy Compared With Placebo on Phagocytic Functioning of Polymorphonuclear (PMN) and Monocyte Cells | This outcome is the mean difference in the % of monocytes that phagocytized E. coli, from blood samples taken at the beginning and end of the trial. Percent of monocytes phagocytizing E. coli at baseline is subtracted by percent of monocytes phagocytizing E. coli at the end of the trial. The mean and standard error are calculated and reported for each study arm. | Some participants were excluded from this analysis due to lack of sample collection, or unusable results because tests did not meet acceptability criteria. | Posted | Mean | Standard Error | Difference in % POS of Monocytes | 4 weeks |
|
|
|
| 0 |
| 18 |
| 9 |
| 18 |
| EG001 | Arm 2: Extra-GI Placebo | Subjects with Extra-GI colonization at initial screening who were randomized to placebo treatment. Placebo composed of identical inactive components to the active product, to be taken once daily for 4 weeks. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. | 2 | 32 | 17 | 32 |
| EG002 | Arm 3: GI Probiotic | Subjects with GI colonization at initial screening who were randomized to probiotic treatment. Subjects were given a capsule formulation of a 1x10^10 colony-forming units of probiotic L. rhamnosus HN001 to be taken once a day, for 4 weeks Lactobacillus rhamnosus HN001: Subjects will be given a pill formulation of a probiotic L. rhamnosus HN001 to be taken once a day, at a dose of 1 x 10^10 organisms | 0 | 34 | 17 | 34 |
| EG003 | Arm 4: GI Placebo | Subjects with GI colonization at initial screening who were randomized to placebo treatment. Placebo composed of identical inactive components to the active product, to be taken once daily for 4 weeks. Placebo pill: composed of identical inactive components to the active product, given to be taken once daily for 4 weeks. | 0 | 29 | 14 | 29 |
| Nausea/Vomiting | Gastrointestinal disorders |
|
| Constipation | Gastrointestinal disorders |
|
| Cough/Cold/Congestion | Respiratory, thoracic and mediastinal disorders |
|
| Muscle Pain/Cramp/Spasm | Musculoskeletal and connective tissue disorders |
|
| Upset Stomach/Heartburn | Gastrointestinal disorders |
|
| Gas/Bloating | Gastrointestinal disorders |
|
| Unusual Stool | Gastrointestinal disorders |
|
| Bad Taste | General disorders |
|
| Itchiness | Skin and subcutaneous tissue disorders |
|
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