search
Back to results

Prevention of Celiac Disease in Skåne (PreCiSe)

Primary Purpose

Celiac Disease in Children

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Gluten free diet
Probiotics
Placebo
Sponsored by
Lund University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Celiac Disease in Children focused on measuring coeliac disease, celiac disease autoimmunity

Eligibility Criteria

4 Months - 4 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Children screened positive for human leucocyte antigen (HLA) DR3-DQ2/DR3-DQ2
  • Children must be enrolled to the study by 4 months of age (before gluten consumption has started).

Exclusion Criteria:

  • Congenital chronic disorder where intervention with diet or probiotics may be affected.
  • Written consent from both caregivers are missing

Sites / Locations

  • Clinical Research Center (CRC), Bldng 60:11Recruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Gluten free diet

Probiotics

Placebo

Arm Description

Gluten free diet

Capsules with a combination of two probiotic bacteria with maize starch as excipient and at a total dose of 10(10) colony forming units (CFU)/capsule.

Placebo capsules with maize starch and without any bacteria.

Outcomes

Primary Outcome Measures

Number of children tested positive for persistent tissue transglutaminase (tTG) autoantibodies, defined as celiac disease autoimmunity
Radioligand binding assays (RBA) will be used to measure tTG autoantibodies in serum samples collected every third months up until the age of 3 years and then annually up until the age of 7 years.

Secondary Outcome Measures

Number of children diagnosed with celiac disease
A celiac disease diagnose will be defined by an intestinal biopsy showing a Marsh score of 2 or higher or by high levels of tTG autoantibodies (> 100 units) in at least 2 consecutive blood samples.

Full Information

First Posted
May 21, 2018
Last Updated
October 3, 2023
Sponsor
Lund University
search

1. Study Identification

Unique Protocol Identification Number
NCT03562221
Brief Title
Prevention of Celiac Disease in Skåne
Acronym
PreCiSe
Official Title
Prevention of Celiac Disease in Skåne (in Swedish - Prevention av Celiaki i Skåne)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 4, 2018 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lund University

4. Oversight

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

5. Study Description

Brief Summary
This study aims to investigate the impact on being on a gluten free diet the first three years of life compared to a daily intake of a probiotic supplementation or placebo on the risk of developing celiac disease autoimmunity or celiac disease in genetically susceptible children. Study participants will be randomly allocated to one of the three study groups before the age of 4 months and will remain in that group with the corresponding intervention during the three first years of life. Regular visits to a study nurse and contact with study dietician will be scheduled. The dietician will support the families in keeping the correct diet intended for each study group.
Detailed Description
The primary hypothesis to be tested is that a strictly gluten free diet during the first three years of life with a slow introduction of gluten during the follow-up period will induce tolerance to gluten. A similar hypothesis is tested if a daily supply of two different lactobacillus (LB) strains can suppress an inflammatory response to gluten in the intestine by stimulating regulatory T-cells and reduced permeability of gluten peptides in the intestine. The secondary hypothesis tested is that celiac disease can not be prevented, but the onset of the disease will be delayed in children returning to a gluten-containing diet after the intervention period (gluten free diet) or probiotic treatment) during the first three years of life. The intervention period is 3 years and the follow-up period is further 4 years. The primary aim is to study the proportion of children who develop celiac disease autoimmunity and progression to celiac disease by the age of 3 years. Secondary aim is to study the proportion of children who developed celiac disease at the age of 7 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Celiac Disease in Children
Keywords
coeliac disease, celiac disease autoimmunity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gluten free diet
Arm Type
Experimental
Arm Description
Gluten free diet
Arm Title
Probiotics
Arm Type
Active Comparator
Arm Description
Capsules with a combination of two probiotic bacteria with maize starch as excipient and at a total dose of 10(10) colony forming units (CFU)/capsule.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo capsules with maize starch and without any bacteria.
Intervention Type
Other
Intervention Name(s)
Gluten free diet
Intervention Description
Controlled gluten free diet
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotics
Intervention Description
Capsules
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Capsules
Primary Outcome Measure Information:
Title
Number of children tested positive for persistent tissue transglutaminase (tTG) autoantibodies, defined as celiac disease autoimmunity
Description
Radioligand binding assays (RBA) will be used to measure tTG autoantibodies in serum samples collected every third months up until the age of 3 years and then annually up until the age of 7 years.
Time Frame
from 4 months of age up until 7 years of age
Secondary Outcome Measure Information:
Title
Number of children diagnosed with celiac disease
Description
A celiac disease diagnose will be defined by an intestinal biopsy showing a Marsh score of 2 or higher or by high levels of tTG autoantibodies (> 100 units) in at least 2 consecutive blood samples.
Time Frame
Up until 7 years of age

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Months
Maximum Age & Unit of Time
4 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children screened positive for human leucocyte antigen (HLA) DR3-DQ2/DR3-DQ2 Children must be enrolled to the study by 4 months of age (before gluten consumption has started). Exclusion Criteria: Congenital chronic disorder where intervention with diet or probiotics may be affected. Written consent from both caregivers are missing
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carin A Aronsson, PhD
Phone
+46708876649
Email
carin.andren_aronsson@med.lu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Agardh, PhD
Organizational Affiliation
Lund University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Research Center (CRC), Bldng 60:11
City
Malmö
ZIP/Postal Code
20502
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carin Andrén Aronsson, PhD
Phone
+46 40391113
Email
carin.andren_aronsson@med.lu.se

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Prevention of Celiac Disease in Skåne

We'll reach out to this number within 24 hrs