SBI in Children With d-IBS
Primary Purpose
Irritable Bowel Syndrome
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Medical Food
Placebo
Sponsored by
About this trial
This is an interventional supportive care trial for Irritable Bowel Syndrome focused on measuring Irritable Bowel Syndrome, Pediatrics, Nutrition
Eligibility Criteria
Inclusion Criteria:
- Males and non-pregnant females between 8 years and 18 years at the time of consent.
- Able to obtain parental or legal guardian informed consent from subjects as applicable.
- d-IBS determined by ROME III criteria. A Rome III diagnosis consists of recurrent abdominal pain or discomfort at least 2days/week in the last 3 months prior to enrollment associated with two or more of the following10:
1. Improvement with defecation 2. Onset associated with a change in frequency of stool 3. Onset associated with a change in form (appearance) of stool.
Exclusion Criteria:
- Children taking pharmacologic treatment for d-IBS will be excluded.
- Children who are unable to articulate symptoms of IBS will be excluded.
- Non-English speaking children will be excluded.
- Children with known allergy or hypersensitivity to beef or any component of SBI.
- Pregnancy.
Sites / Locations
- Childrens Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
SBI
Placebo
Arm Description
Entergam 10 g/day PO
Placebo 10 g/day PO
Outcomes
Primary Outcome Measures
Number of spontaneous bowel movements
The primary outcome will be change in the number of spontaneous bowel movements from the screening week compared to the final week. This information is gathered as part of the daily diary questions.
Secondary Outcome Measures
Stool consistency
Bristol Stool Scale
Laboratory values
Stool calprotectin, stool lactoferrin, ESR, CRP, platelet count
Psychosocial
Pediatric Quality of Life Inventory
Full Information
NCT ID
NCT02609529
First Posted
November 17, 2015
Last Updated
March 8, 2017
Sponsor
Louisiana State University Health Sciences Center in New Orleans
Collaborators
Entera Health, Inc
1. Study Identification
Unique Protocol Identification Number
NCT02609529
Brief Title
SBI in Children With d-IBS
Official Title
Double-Blind, Randomized Pilot Study Evaluating Oral Serum-Derived Bovine Immunoglobulin Protein Isolate (SBI) on Nutritional Status in Children With Diarrhea-Predominant Irritable Bowel Syndrome (d-IBS)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
March 2, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Louisiana State University Health Sciences Center in New Orleans
Collaborators
Entera Health, Inc
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
IBS is the most common diagnosis in new patients in our pediatric gastroenterology clinic, accounting for 36 % of all new patients. Pediatric IBS patients always have a problem with defecation, characterized either as diarrhea predominant or constipation predominant. About one third of pediatric IBS subjects have d-IBS. There are no FDA approved treatments for children with d-IBS. There is evidence that diarrhea predominant irritable bowel syndrome d-IBS may be caused by a mild inflammation in the intestinal lining. Oral serum-derived bovine immunoglobulin protein isolate (SBI) is a medical food, believed to treat mild inflammation in the small intestine associated with some cases of d-IBS, especially those arising after acute gastroenteritis. It improved pain and diarrhea in adults with d-IBS. Our aim is to determine if SBI improves the number of spontaneous bowel movements in children with d-IBS.
Detailed Description
The objectives of the study are to determine whether there is improvement in gastrointestinal symptoms (i.e., number of spontaneous bowel movements. abdominal pain, stool consistency, reduction in stool number, flatulence, urgency, incontinence), in laboratory parameters, and/or in psychosocial measures in subjects with d-IBS receiving 3 weeks of SBI.
This is a randomized, double-blind, placebo-controlled, weighted, pilot study evaluating effects of SBI (10 g per day), in children or adolescents with d-IBS.
The primary outcome will be change in the number of spontaneous bowel movements from the screening week compared to the final week. This information is gathered as part of the daily diary questions.
Secondary clinical outcome variables will include changes in abdominal pain, stool consistency, flatulence, urgency, and incontinence. Further clinical outcome variables will be change in number of spontaneous bowel movements during each treatment week compared to the screening week. Stool consistency will be assessed with the Bristol Stool Form Scale. Secondary laboratory outcome variables will include changes in stool calprotectin, stool lactoferrin, erythrocyte sedimentation rate, C-reactive protein, and platelet count from the screening week and final week. Secondary psychosocial outcomes will include data from Pediatric Quality of Life Inventory for Gastrointestinal Symptoms, and the Pediatric Functional Disability Index.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
Keywords
Irritable Bowel Syndrome, Pediatrics, Nutrition
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SBI
Arm Type
Experimental
Arm Description
Entergam 10 g/day PO
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo 10 g/day PO
Intervention Type
Other
Intervention Name(s)
Medical Food
Other Intervention Name(s)
Enteragam
Intervention Description
Serum-derived bovine immunoglobulin protein isolate will be supplied by EnteraHealth. The product is manufactured in accordance with Good Manufacturing Practice (GMP) and U.S. Food and Drug Administration (FDA) guidelines for medical food ingredients (21 CFR Part 110). Serum-derived bovine immunoglobulin protein isolate (SBI) is generally recognized as safe (GRAS). The FDA has reviewed the safety dossier for SBI as a medical food product.
Intervention Type
Other
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Number of spontaneous bowel movements
Description
The primary outcome will be change in the number of spontaneous bowel movements from the screening week compared to the final week. This information is gathered as part of the daily diary questions.
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Stool consistency
Description
Bristol Stool Scale
Time Frame
3 weeks
Title
Laboratory values
Description
Stool calprotectin, stool lactoferrin, ESR, CRP, platelet count
Time Frame
3 weeks
Title
Psychosocial
Description
Pediatric Quality of Life Inventory
Time Frame
3 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Males and non-pregnant females between 8 years and 18 years at the time of consent.
Able to obtain parental or legal guardian informed consent from subjects as applicable.
d-IBS determined by ROME III criteria. A Rome III diagnosis consists of recurrent abdominal pain or discomfort at least 2days/week in the last 3 months prior to enrollment associated with two or more of the following10:
1. Improvement with defecation 2. Onset associated with a change in frequency of stool 3. Onset associated with a change in form (appearance) of stool.
Exclusion Criteria:
Children taking pharmacologic treatment for d-IBS will be excluded.
Children who are unable to articulate symptoms of IBS will be excluded.
Non-English speaking children will be excluded.
Children with known allergy or hypersensitivity to beef or any component of SBI.
Pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Hyman, MD
Organizational Affiliation
LSUHSC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Childrens Hospital
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70118
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24485818
Citation
Giannetti E, de'Angelis G, Turco R, Campanozzi A, Pensabene L, Salvatore S, de Seta F, Staiano A. Subtypes of irritable bowel syndrome in children: prevalence at diagnosis and at follow-up. J Pediatr. 2014 May;164(5):1099-1103.e1. doi: 10.1016/j.jpeds.2013.12.043. Epub 2014 Jan 31.
Results Reference
background
PubMed Identifier
22837345
Citation
Camilleri M, Lasch K, Zhou W. Irritable bowel syndrome: methods, mechanisms, and pathophysiology. The confluence of increased permeability, inflammation, and pain in irritable bowel syndrome. Am J Physiol Gastrointest Liver Physiol. 2012 Oct;303(7):G775-85. doi: 10.1152/ajpgi.00155.2012. Epub 2012 Jul 26.
Results Reference
background
PubMed Identifier
23660579
Citation
Asmuth DM, Ma ZM, Albanese A, Sandler NG, Devaraj S, Knight TH, Flynn NM, Yotter T, Garcia JC, Tsuchida E, Wu TT, Douek DC, Miller CJ. Oral serum-derived bovine immunoglobulin improves duodenal immune reconstitution and absorption function in patients with HIV enteropathy. AIDS. 2013 Sep 10;27(14):2207-17. doi: 10.1097/QAD.0b013e328362e54c.
Results Reference
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PubMed Identifier
10613760
Citation
Jiang R, Chang X, Stoll B, Fan MZ, Arthington J, Weaver E, Campbell J, Burrin DG. Dietary plasma protein reduces small intestinal growth and lamina propria cell density in early weaned pigs. J Nutr. 2000 Jan;130(1):21-6. doi: 10.1093/jn/130.1.21.
Results Reference
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PubMed Identifier
15217004
Citation
Bosi P, Casini L, Finamore A, Cremokolini C, Merialdi G, Trevisi P, Nobili F, Mengheri E. Spray-dried plasma improves growth performance and reduces inflammatory status of weaned pigs challenged with enterotoxigenic Escherichia coli K88. J Anim Sci. 2004 Jun;82(6):1764-72. doi: 10.2527/2004.8261764x.
Results Reference
background
PubMed Identifier
24833942
Citation
Wilson D, Evans M, Weaver E, Shaw AL, Klein GL. Evaluation of serum-derived bovine immunoglobulin protein isolate in subjects with diarrhea-predominant irritable bowel syndrome. Clin Med Insights Gastroenterol. 2013 Dec 5;6:49-60. doi: 10.4137/CGast.S13200. eCollection 2013.
Results Reference
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PubMed Identifier
1826329
Citation
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Results Reference
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PubMed Identifier
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Citation
Varni JW, Kay MT, Limbers CA, Franciosi JP, Pohl JF. PedsQL gastrointestinal symptoms module item development: qualitative methods. J Pediatr Gastroenterol Nutr. 2012 May;54(5):664-71. doi: 10.1097/MPG.0b013e31823c9b88.
Results Reference
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SBI in Children With d-IBS
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