Study of Enzyme Supplements to Treat Celiac Disease
Primary Purpose
Celiac Disease, Dermatitis Herpetiformis
Status
Completed
Phase
Phase 1
Locations
Hungary
Study Type
Interventional
Intervention
STAN1
Placebo enzyme
STAN1+gluten
Sponsored by
About this trial
This is an interventional treatment trial for Celiac Disease focused on measuring celiac disease, transglutaminase antibody
Eligibility Criteria
Inclusion Criteria:
- Celiac disease diagnosed by small intestinal biopsy
- More than 12 months elapsed since initial diagnosis and start of the dietary treatment
- Evidence for ongoing active disease as verified by seropositivity or dermatitis herpetiformis rash
- Subject agrees to follow a gluten-free diet
Exclusion Criteria:
- Other gastrointestinal or hepatic disease besides celiac disease
- Selective IgA deficiency
- Use of dapsone or diaphenylsulfone
- Pregnancy and breast-feeding
Sites / Locations
- Heim Pal Children's Hospital
- University of Debrecen
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
Experimental
Arm Label
Enzyme treatment
Placebo control
Enzyme + gluten
Arm Description
Enzyme for 12 weeks
Placebo enzyme for 12 weeks
Enzyme and 500 mg gluten b.i.d. for 12 weeks
Outcomes
Primary Outcome Measures
Negative seroconversion or a drop of more than 50% in anti-transglutaminase antibody blood levels by ELISA
Secondary Outcome Measures
Negative seroconversion or drop of at least two dilution steps in the EMA test
Negative conversion for celiac antibodies in the blood by the rapid test
Change in symptoms or rash (if any)
Favorable changes in morphometry in small bowel biopsy specimens
Full Information
NCT ID
NCT00962182
First Posted
August 18, 2009
Last Updated
March 4, 2018
Sponsor
Heim Pal Children's Hospital
Collaborators
Stanford University
1. Study Identification
Unique Protocol Identification Number
NCT00962182
Brief Title
Study of Enzyme Supplements to Treat Celiac Disease
Official Title
Effect of a Cocktail of Two Common Enzyme Supplements on Celiac Disease Patients With Persistent Seropositivity
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Heim Pal Children's Hospital
Collaborators
Stanford University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to examine whether a cocktail of two common food-grade enzyme supplements leads to decrease of serum activity markers in celiac disease patients insufficiently treated by previous gluten exclusion.
Detailed Description
Celiac disease is genetically determined abnormal immune response to gluten, a component of wheat, rye and barley proteins that cause damage to the villous structure in the small bowel. The active disease is characterized by the induction of gluten-dependent autoantibodies to transglutaminase type-2, which are sensitive and specific non-invasive markers of gluten-sensitivity. Gluten-free diet normally leads to clearance of antibodies from serum in 6-12 months. Persistent seropositivity is a problem in patients who only incompletely exclude gluten or frequently transgress the diet. In such cases, damage of the small bowel may persist and complications may occur at higher frequency. The central hypothesis to be tested is that enzyme treatment designed to degrade a certain amount of gluten before absorption in the gastrointestinal tract will lead to a clinically meaningful decrease in auto-antibody levels in these patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Celiac Disease, Dermatitis Herpetiformis
Keywords
celiac disease, transglutaminase antibody
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
38 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Enzyme treatment
Arm Type
Experimental
Arm Description
Enzyme for 12 weeks
Arm Title
Placebo control
Arm Type
Placebo Comparator
Arm Description
Placebo enzyme for 12 weeks
Arm Title
Enzyme + gluten
Arm Type
Experimental
Arm Description
Enzyme and 500 mg gluten b.i.d. for 12 weeks
Intervention Type
Drug
Intervention Name(s)
STAN1
Intervention Description
3-4 capsules/day at meals
Intervention Type
Drug
Intervention Name(s)
Placebo enzyme
Intervention Description
3-4 capsules/day at meals
Intervention Type
Drug
Intervention Name(s)
STAN1+gluten
Intervention Description
3-4 capsules/day at meals plus 500 mg gluten b.i.d
Primary Outcome Measure Information:
Title
Negative seroconversion or a drop of more than 50% in anti-transglutaminase antibody blood levels by ELISA
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Negative seroconversion or drop of at least two dilution steps in the EMA test
Time Frame
12 weeks
Title
Negative conversion for celiac antibodies in the blood by the rapid test
Time Frame
12 weeks
Title
Change in symptoms or rash (if any)
Time Frame
12 weeks
Title
Favorable changes in morphometry in small bowel biopsy specimens
Time Frame
28 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Celiac disease diagnosed by small intestinal biopsy
More than 12 months elapsed since initial diagnosis and start of the dietary treatment
Evidence for ongoing active disease as verified by seropositivity or dermatitis herpetiformis rash
Subject agrees to follow a gluten-free diet
Exclusion Criteria:
Other gastrointestinal or hepatic disease besides celiac disease
Selective IgA deficiency
Use of dapsone or diaphenylsulfone
Pregnancy and breast-feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ilma Korponay-Szabo, M.D., Ph.D.
Organizational Affiliation
Heim Pal Children's Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Heim Pal Children's Hospital
City
Budapest
ZIP/Postal Code
1089
Country
Hungary
Facility Name
University of Debrecen
City
Debrecen
ZIP/Postal Code
H-4032
Country
Hungary
12. IPD Sharing Statement
Learn more about this trial
Study of Enzyme Supplements to Treat Celiac Disease
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