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Prebiotic as a Supplement of Gluten-free Diet in the Management of Celiac Disease in Children

Primary Purpose

Celiac Disease

Status
Completed
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Synergy 1
Placebo
Sponsored by
Polish Academy of Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Celiac Disease focused on measuring prebiotic, pediatric patients, health status, intestine permeability

Eligibility Criteria

3 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • celiac disease
  • treatment with gluten-free diet for at least 6 months
  • general good health
  • the written informed consent to participate the study

Exclusion Criteria:

  • participation in another study involving prebiotic and/or probiotic preparations, or intention to use such products during the course of the study
  • other gastrointestinal diseases
  • received antibiotics in the previous month
  • use of dietary supplements containing prebiotic or/and probiotic within the previous month
  • bad or average overall health

Sites / Locations

  • Regional Specialized Children'S Hospital
  • Institute of Animal Reproduction and Food Research, Polish Academy of Sciences in Olsztyn

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Prebiotic Synergy 1-supplemented GFD

Placebo-supplemented GFD

Arm Description

The application of a prebiotic Synergy 1 together with a strict gluten-free diet

The application of a placebo together with a strict gluten-free diet

Outcomes

Primary Outcome Measures

Assessment of the intestinal permeability
Changes in the concentration of intestinal fatty acid binding protein (iFABP) as a biomarker of intestinal permeability will be determined

Secondary Outcome Measures

Assessment of the advers events
A number of participants with adverse events related to the treatment will be recorded
Analysis of the concentration of the short chain fatty acids (SCFAs)
Changes in the concentration and a profile of the short chain fatty acids (SCFAs) using gas chromatography
Molecular characteristic of faecal microbiota
Quantitative characteristics of faecal bacteria will be conducted with the real-time polymerase chain reaction (RT-PCR) technique and group-specific primers. Population level of Bifidobacterium, Bacteroides, Clostridium coccoides, C. leptum and E. coli groups will be determined among others.

Full Information

First Posted
February 16, 2017
Last Updated
October 25, 2019
Sponsor
Polish Academy of Sciences
Collaborators
University of Warmia and Mazury
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1. Study Identification

Unique Protocol Identification Number
NCT03064997
Brief Title
Prebiotic as a Supplement of Gluten-free Diet in the Management of Celiac Disease in Children
Official Title
Assessment of the Impact of Prebiotic Synergy 1 on the Intestine Permeability, Clinical Symptoms, and Selected Biochemical and Nutritional Parameters in the Children With Celiac Disease on a Gluten-free Diet
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
January 12, 2016 (Actual)
Primary Completion Date
March 1, 2016 (Actual)
Study Completion Date
June 1, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Polish Academy of Sciences
Collaborators
University of Warmia and Mazury

4. Oversight

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

5. Study Description

Brief Summary
Prebiotics are known as substances affecting beneficially the organism by restoring the intestinal microbiota balance, stabilizing the intestinal barrier and modulating the endocrine and immune functions. In many persons suffering from celiac disease (CD), despite a gluten-free diet (GFD), an impaired intestinal barrier functionality, accompanied by altered intestinal microbiota and ongoing intestinal inflammation is observed. For these reasons, prebiotic could be a promising and low-risk adjuvant in the dietetic management of CD. It was hypothesize that prebiotic preparation Synergy 1 consumed by CD children as a supplement of a GFD will affect beneficial the intestinal permeability and intestinal microbiota without side effects.
Detailed Description
Prebiotics, including inulin-type fructans (ITFs) are a group of the naturally occurring plant carbohydrates stored in various amounts in tubers, bulbs and tuberous roots of several edible fruits and vegetables and in particularly large amounts in the tubers of Helianthus tuberosus (Jerusalem artichoke) and Cichorium intybus (chicory). Because of their unique structural properties, they are not hydrolyzed by the enzymes of the upper intestinal digestive tract and reach the colon unchanged, therefore are classified as prebiotics. Prebiotics are defined as selectively fermented ingredients that allow specific changes in the composition and/or balance of the microbiota. ITFs, particularly the mixture of short- and long-chain polymers, indicate several beneficial effects, including the positive changes in the histological picture of the intestine (proliferation in the crypts and Goblet cells, longer intestinal villi) and modulation of the endocrine and immune functions. Moreover, they have a great potential as agents improving or maintaining a balanced intestinal microbiota both in the lumen and at the mucosal surface, to one in which bifidobacteria and lactobacilli come to greater prominence. This, so-called healthier flora, should provide increased resistance to gut infections and may also have immuno-modulatory properties. Until now, inulin and fructooligosaccharide (FOS) have been tested mainly in animal models of inflammatory bowel diseases (IBD). Reports on animal colitis model suggests that prebiotics have the anti-inflammatory properties as they reduce the inflammation symptoms, along with the increase in bifidobacteria or lactobacilli number, and in some reports, the increase in the concentration of butyrate in the gut. Prebiotics are known as substances affecting beneficially the organism by restoring the intestinal microbiota balance, stabilizing the intestinal barrier and modulating the endocrine and immune functions. In many persons suffering from celiac disease (CD), despite a gluten-free diet (GFD), an impaired intestinal barrier functionality, accompanied by altered intestinal microbiota and ongoing intestinal inflammation is observed. For these reasons, prebiotics could be a promising and low-risk adjuvant in the dietetic management of CD. It was hypothesized that Synergy 1 consumed by CD children as a supplement of a GFD will affect beneficial the intestinal permeability and intestinal microbiota without side effects. The primary objective of this randomized placebo-controlled study was to determine the effect of 3-months consumption of Synergy 1 versus placebo, as the supplements of a GFD, on the intestinal permeability in CD children, in particular on the concentration of the intestinal fatty acid binding protein (iFABP) as a biomarker of intestinal permeability. The secondary objective was to determine the effect of Synergy 1 versus placebo applied in GFD on the changes in the gut microbiota quantity and metabolism in CD children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Celiac Disease
Keywords
prebiotic, pediatric patients, health status, intestine permeability

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prebiotic Synergy 1-supplemented GFD
Arm Type
Active Comparator
Arm Description
The application of a prebiotic Synergy 1 together with a strict gluten-free diet
Arm Title
Placebo-supplemented GFD
Arm Type
Placebo Comparator
Arm Description
The application of a placebo together with a strict gluten-free diet
Intervention Type
Dietary Supplement
Intervention Name(s)
Synergy 1
Intervention Description
a daily dose: 7 g/day of Synergy1 (oligofructose enriched inulin) consumed for 12 weeks together with a strict gluten-free diet
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
a daily dose: 7 g/day of placebo (maltodextrin) consumed for 12 weeks together with a strict gluten-free diet
Primary Outcome Measure Information:
Title
Assessment of the intestinal permeability
Description
Changes in the concentration of intestinal fatty acid binding protein (iFABP) as a biomarker of intestinal permeability will be determined
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Assessment of the advers events
Description
A number of participants with adverse events related to the treatment will be recorded
Time Frame
6 months
Title
Analysis of the concentration of the short chain fatty acids (SCFAs)
Description
Changes in the concentration and a profile of the short chain fatty acids (SCFAs) using gas chromatography
Time Frame
6 month
Title
Molecular characteristic of faecal microbiota
Description
Quantitative characteristics of faecal bacteria will be conducted with the real-time polymerase chain reaction (RT-PCR) technique and group-specific primers. Population level of Bifidobacterium, Bacteroides, Clostridium coccoides, C. leptum and E. coli groups will be determined among others.
Time Frame
6 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: celiac disease treatment with gluten-free diet for at least 6 months general good health the written informed consent to participate the study Exclusion Criteria: participation in another study involving prebiotic and/or probiotic preparations, or intention to use such products during the course of the study other gastrointestinal diseases received antibiotics in the previous month use of dietary supplements containing prebiotic or/and probiotic within the previous month bad or average overall health
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Urszula Krupa-Kozak, Ph.D
Organizational Affiliation
Institute of Animal Reproduction and Food Reseach, Polish Academy of Sciences in Olsztyn
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Elżbieta Jarocka-Cyrta, MD, Ph.D
Organizational Affiliation
Department of Clinical Pediatrics, Faculty of Medical Sciences, University of Warmia and Mazury
Official's Role
Principal Investigator
Facility Information:
Facility Name
Regional Specialized Children'S Hospital
City
Olsztyn
ZIP/Postal Code
10-561
Country
Poland
Facility Name
Institute of Animal Reproduction and Food Research, Polish Academy of Sciences in Olsztyn
City
Olsztyn
ZIP/Postal Code
10-748
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30959740
Citation
Drabinska N, Jarocka-Cyrta E, Ratcliffe NM, Krupa-Kozak U. The Profile of Urinary Headspace Volatile Organic Compounds After 12-Week Intake of Oligofructose-Enriched Inulin by Children and Adolescents with Celiac Disease on a Gluten-Free Diet: Results of a Pilot, Randomized, Placebo-Controlled Clinical Trial. Molecules. 2019 Apr 5;24(7):1341. doi: 10.3390/molecules24071341.
Results Reference
result
PubMed Identifier
30840918
Citation
Drabinska N, Jarocka-Cyrta E, Zlotkowska D, Abramowicz P, Krupa-Kozak U. Daily oligofructose-enriched inulin intake impacts bone turnover markers but not the cytokine profile in pediatric patients with celiac disease on a gluten-free diet: Results of a randomised, placebo-controlled pilot study. Bone. 2019 May;122:184-192. doi: 10.1016/j.bone.2019.03.001. Epub 2019 Mar 3.
Results Reference
result
PubMed Identifier
30469412
Citation
Ferus K, Drabinska N, Krupa-Kozak U, Jarocka-Cyrta E. A Randomized, Placebo-Controlled, Pilot Clinical Trial to Evaluate the Effect of Supplementation with Prebiotic Synergy 1 on Iron Homeostasis in Children and Adolescents with Celiac Disease Treated with a Gluten-Free Diet. Nutrients. 2018 Nov 21;10(11):1818. doi: 10.3390/nu10111818.
Results Reference
result
PubMed Identifier
30445682
Citation
Drabinska N, Krupa-Kozak U, Abramowicz P, Jarocka-Cyrta E. Beneficial Effect of Oligofructose-Enriched Inulin on Vitamin D and E Status in Children with Celiac Disease on a Long-Term Gluten-Free Diet: A Preliminary Randomized, Placebo-Controlled Nutritional Intervention Study. Nutrients. 2018 Nov 15;10(11):1768. doi: 10.3390/nu10111768.
Results Reference
result
PubMed Identifier
30043079
Citation
Drabinska N, Krupa-Kozak U, Ciska E, Jarocka-Cyrta E. Plasma profile and urine excretion of amino acids in children with celiac disease on gluten-free diet after oligofructose-enriched inulin intervention: results of a randomised placebo-controlled pilot study. Amino Acids. 2018 Oct;50(10):1451-1460. doi: 10.1007/s00726-018-2622-7. Epub 2018 Jul 24.
Results Reference
result
PubMed Identifier
29439526
Citation
Drabinska N, Jarocka-Cyrta E, Markiewicz LH, Krupa-Kozak U. The Effect of Oligofructose-Enriched Inulin on Faecal Bacterial Counts and Microbiota-Associated Characteristics in Celiac Disease Children Following a Gluten-Free Diet: Results of a Randomized, Placebo-Controlled Trial. Nutrients. 2018 Feb 12;10(2):201. doi: 10.3390/nu10020201.
Results Reference
result
PubMed Identifier
28830428
Citation
Krupa-Kozak U, Drabinska N, Jarocka-Cyrta E. The effect of oligofructose-enriched inulin supplementation on gut microbiota, nutritional status and gastrointestinal symptoms in paediatric coeliac disease patients on a gluten-free diet: study protocol for a pilot randomized controlled trial. Nutr J. 2017 Aug 22;16(1):47. doi: 10.1186/s12937-017-0268-z.
Results Reference
derived

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Prebiotic as a Supplement of Gluten-free Diet in the Management of Celiac Disease in Children

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