Use of SBI in IBS Subjects Following a Successful Treatment of Small Intestinal Bacterial Overgrowth
Primary Purpose
Diarrhea Predominant Irritable Bowel Syndrome, Small Intestinal Bacterial Overgrowth
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Serum-derived bovine immunoglobulin protein isolate (SBI)
Placebo
Sponsored by
About this trial
This is an interventional supportive care trial for Diarrhea Predominant Irritable Bowel Syndrome focused on measuring DIBS, SIBO
Eligibility Criteria
Inclusion Criteria:
- Male or female aged 18-75 years old
- Meet Rome II criteria for IBS-D
- Meet criteria for SIBO
- If ≥50 years old, a colonoscopy must have been completed within the past 10 years
- Have just completed a course of antibiotic treatment with rifaximin and successfully responded to this treatment.
Exclusion Criteria:
- Had intestinal surgery (except appendectomy or cholecystectomy)
- Pelvic floor dysfunction
- Pregnancy or nursing mothers
- History of bowel obstruction
- History of celiac disease
- History of inflammatory bowel disease
- Cirrhosis
- Diabetes
- Use of tricyclic antidepressants
- Use of antidiarrheal medications
- Allergy or hypersensitivity to beef or any component of SBI
Sites / Locations
- GI Motility Program Cedars-Sinai Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Placebo Comparator
Arm Label
SBI
Placebo
Arm Description
Group 1: SBI (N=30) - one packet daily
Group 2: Placebo (N=30) - one packet daily
Outcomes
Primary Outcome Measures
Time to relapse (symptom recurrence) in subjects with IBS-D after successful treatment with rifaximin
Secondary Outcome Measures
Change in symptoms based on comparison of baseline symptom questionnaire to weekly symptom questionnaires
Comparison of baseline Bristol stool score based on 7 day stool diary
Comparison of KT ratios in plasma samples
Full Information
NCT ID
NCT02251483
First Posted
September 17, 2014
Last Updated
July 27, 2015
Sponsor
Cedars-Sinai Medical Center
Collaborators
Entera Health, Inc
1. Study Identification
Unique Protocol Identification Number
NCT02251483
Brief Title
Use of SBI in IBS Subjects Following a Successful Treatment of Small Intestinal Bacterial Overgrowth
Official Title
Use of Serum-derived Immunoglobulin/Protein Isolate (SBI) for the Maintenance of Health in Subjects With Irritable Bowel Syndrome (IBS) Following Successful Treatment of Small Intestinal Bacterial Overgrowth (SIBO)
Study Type
Interventional
2. Study Status
Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cedars-Sinai Medical Center
Collaborators
Entera Health, Inc
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary objective of this study is to determine whether giving SBI as a medical food starting with maintenance of health in the management of chronic loose and frequent stools in IBS-D subjects with SIBO after successful treatment with rifaximin can lead to more prolonged duration of benefit and delay symptom recurrence. SBI is the main ingredient in EnteraGam™, an orally administered prescription medical food for the dietary management of patients with enteropathy or chronic loose or frequent stools, including patients with IBS-D.
Detailed Description
Irritable bowel syndrome (IBS) is one of the most common gastrointestinal disorders, with a global prevalence of 11%. IBS manifests itself in 3 major forms; diarrhea-predominant (IBS-D), constipation-predominant (IBS-C), and mixed (IBS-M), and is predominantly characterized by symptoms of abdominal pain, changes in stool frequency and consistency, and abdominal bloating.
SIBO is a condition in which there is an increase in the number of bacteria in the small bowel, and typically includes an overgrowth of coliform bacteria which are normally found in the colon. These ferment carbohydrates into gas (which can be measured using the lactulose breath test (LBT)), and the SIBO hypothesis proposes that it is this expansion of bacteria in the small bowel that leads to IBS symptoms including bloating, abdominal discomfort and changes in stool form. The antibiotic rifaximin is used to treat IBS-D, and has been shown to normalize the LBT in 70% of subjects. Despite this success, symptoms such as SIBO tend to recur, usually within 4 months of finishing the antibiotic treatment. Therefore, there remains a significant need to identify therapeutic agents which can maintain the health of subjects with IBS and SIBO and increase the duration of benefit in subjects with IBS and SIBO following antibiotic treatment.
SBI is intended for the dietary management of enteropathy under medical supervision in patients with chronic loose or frequent stools, including IBS-D patients. In vitro and animal studies have shown that SBI supports digestive and absorptive properties of the intestinal tracts by:
Binding and neutralizing microbial components
Helping to maintain beneficial gut microbiota
Managing gut barrier function
Maintaining GI immune balance
Clinical studies have also demonstrated that oral SBI improves nutrient absorption, nutritional status and GI symptoms in patients with HIV-associated enteropathy, IBS-D, or malnutrition. It is important to note that SBI is not used to treat patients with IBS-D or other enteropathies, but is given as a medical food to assist in the maintenance of health only.
This study will assess whether giving SBI as a medical food to subjects with IBS-D and SIBO after they successfully complete a course of rifaximin can lead to more prolonged maintenance of health and duration of benefit of antibiotic treatment in IBS-D patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhea Predominant Irritable Bowel Syndrome, Small Intestinal Bacterial Overgrowth
Keywords
DIBS, SIBO
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SBI
Arm Type
Other
Arm Description
Group 1: SBI (N=30) - one packet daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Group 2: Placebo (N=30) - one packet daily
Intervention Type
Other
Intervention Name(s)
Serum-derived bovine immunoglobulin protein isolate (SBI)
Intervention Type
Other
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Time to relapse (symptom recurrence) in subjects with IBS-D after successful treatment with rifaximin
Time Frame
up to 4 months
Secondary Outcome Measure Information:
Title
Change in symptoms based on comparison of baseline symptom questionnaire to weekly symptom questionnaires
Time Frame
baseline and weekly questionnaires for up to 4 months
Title
Comparison of baseline Bristol stool score based on 7 day stool diary
Time Frame
last week of every month for up to 4 months
Title
Comparison of KT ratios in plasma samples
Time Frame
up to 4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female aged 18-75 years old
Meet Rome II criteria for IBS-D
Meet criteria for SIBO
If ≥50 years old, a colonoscopy must have been completed within the past 10 years
Have just completed a course of antibiotic treatment with rifaximin and successfully responded to this treatment.
Exclusion Criteria:
Had intestinal surgery (except appendectomy or cholecystectomy)
Pelvic floor dysfunction
Pregnancy or nursing mothers
History of bowel obstruction
History of celiac disease
History of inflammatory bowel disease
Cirrhosis
Diabetes
Use of tricyclic antidepressants
Use of antidiarrheal medications
Allergy or hypersensitivity to beef or any component of SBI
Facility Information:
Facility Name
GI Motility Program Cedars-Sinai Medical Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Use of SBI in IBS Subjects Following a Successful Treatment of Small Intestinal Bacterial Overgrowth
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