Skip to main content
OpenTrials
Completed

NCT Number: NCT06151782

Immunosafe-CeD: Are Partially Hydrolysed Gluten Harmful to Celiac Disease Patients?

The study will compare the immune response in CeD patients to wheat and barley gluten at high doses (1 gram), and also investigate the reponses to low dose barley gluten and also hydrolyzed, malted barley and placebo. This will be done by five one-day challenges with intervals around four weeks.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinical Center for Celiac Disease and Autoimmunity, Mainz, Germany

Loading trial locations.

About this study

Celiac disease (CeD) is a common food-induced inflammatory disease of the small intestine caused by the ingestion of gluten from wheat, barley and rye. It is one of the most prevalent food hypersensitivities worldwide and affects 0.5-2.5% of the European population. The only effective treatment available is a strict lifelong gluten-free (GF) diet. GF products for CeD patients must not exceed the regulatory threshold of 20 mg/kg of gluten. Compliance of foods containing fermented or partially hydrolysed gluten is routinely assessed using the R5 competitive enzyme-linked immunosorbent assay (ELISA). However, this test does not adequately represent gluten immunogenicity in CeD patients. The overall objective of our ImmunoSafe-CeD proposal is to determine the CeD immunogenic activity of intact and partially hydrolysed gluten from wheat, rye and barley and develop improved comprehensive functional and analytical assays, including novel ELISAs and quantitative proteomics methods to ensure food safety for CeD patients. Thus, our objective is designed to directly address the needs of the CeD community about being reassured that GF products that contain partially hydrolysed gluten are safe and suitable for inclusion in their GF diet. By combining discovery proteomics and quantitative LC-MS/MS methods, improved reference materials for partially hydrolysed gluten, CeD-patient derived monoclonal antibodies and functional gluten-specific T-cell assays, we will provide a comprehensive and unique toolbox of novel and validated methods to detect gluten (both intact and partially hydrolysed) in foods for CeD patients.

This toolbox will close the current discrepancy between food analytical methods and CeD immunogenicity for the first time, because all methods will be matched to clinical pathophysiology assessed by food challenge in CeD patients. Our multidisciplinary consortium is built on previous highly successful collaborations and we are well-positioned to create even more synergies between us by exchanging materials, know-how and data. We expect to 1) better understand the role that the different glutens play in CeD pathogenesis, 2) develop easy-to-perform and reliable analytical tools (ELISA) that quantitate and predict immunogenicity (toxicity) of wheat, rye and barley products for CeD patients, and 3) define foods that CeD patients can tolerate despite being partly based on these processed grains

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI between 18 and 30 kg/m2
  • Biopsy verified celiac disease
  • Pos gene test for HLA-DQ2.5 or DQ8
  • Strict glutenfree diet for at least 24 months
  • Clinical remission
  • Sensitive to gluten by accidental intake
  • Effective contraception if female in fertile age

Exclusion criteria

  • Positive serology at screening
  • Pregnant or lactating
  • Other disease like Type 1 diabetes, cardiovascular disease, cancer, inflammatory bowel disease, thyroid or kidney disease
  • On immunosuppressive drugs
  • Smoking
  • Food allergy including wheat allergy
  • Acute infection

Treatment and study plan

Wheat gluten 1000 mg

Dietary Supplement

Nothing to add here

Barley gluten 1000 mg

Dietary Supplement

Nothing to add here

Barley gluten 50 mg

Dietary Supplement

Nothing to add here

Barley hydrolyzed gluten 50 mg

Dietary Supplement

Nothing to add here

Placebo slurry

Dietary Supplement

In slurry, measurement of immune activation (Interleukin-2) four hours after intake

Primary outcomes

  1. Interleukin-2 in serum

    Time frame: 4 hours after intake

    Cytokine measurement by MSD Mesoscale

Secondary outcomes

  1. GIP in urine 4 hours after challenge and feces 2 days after challenge

    Time frame: Four hours after challenge (urine) and 2 days after challenge (feces)

    Detection of gluten by test kits for BioMedal

  2. Immune reaction to wheat and barley

    Time frame: Before each patient has been challenged

    Whole-blood cytokine release assay where blood is challenged with gluten peptides

  3. PROM

    Time frame: At baseline and at each of the five challenges; at time 0, 1hour, 2hours, 3hours and 4hours after the challenge. We use a VAS score and the GSRS form.

    Gastrointestinal symptom score after challenge assessed scoring forms

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Registry information

Official study title

Towards Comprehensive Analytical Methods for Partially Hydrolysed Gluten to Assess Product Safety for Celiac Disease Patients

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 30, 2023
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.