PreCiSe: Prevention of Celiac Disease in Skåne

Sponsor
Lund University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03562221
Collaborator
(none)
600
1
3
103.9
5.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Gluten free diet
  • Dietary Supplement: Probiotics
  • Dietary Supplement: Placebo
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
600 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Primary Purpose:
Prevention
Official Title:
Prevention of Celiac Disease in Skåne (in Swedish - Prevention av Celiaki i Skåne)
Actual Study Start Date :
Dec 4, 2018
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Gluten free diet

Gluten free diet

Other: Gluten free diet
Controlled gluten free diet

Active Comparator: Probiotics

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.

Dietary Supplement: Probiotics
Capsules

Placebo Comparator: Placebo

Placebo capsules with maize starch and without any bacteria.

Dietary Supplement: Placebo
Capsules

Outcome Measures

Primary Outcome Measures

  1. Number of children tested positive for persistent tissue transglutaminase (tTG) autoantibodies, defined as celiac disease autoimmunity [from 4 months of age up until 7 years of age]

    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

  1. Number of children diagnosed with celiac disease [Up until 7 years of age]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Months to 4 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical Research Center (CRC), Bldng 60:11 Malmö Sweden 20502

Sponsors and Collaborators

  • Lund University

Investigators

  • Principal Investigator: Daniel Agardh, PhD, Lund University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lund University
ClinicalTrials.gov Identifier:
NCT03562221
Other Study ID Numbers:
  • 2018/61
First Posted:
Jun 19, 2018
Last Update Posted:
Apr 6, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lund University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 6, 2022