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Not yet recruiting NCT07578038

Interest of Urinary Measurement of Immunogenic Gluten Peptides (GIP) in the Follow-up of Pediatric Celiac Patients.

No phase Interventional Coeliac Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Urinary measurement of GIP, Usual follow-up and measurement of urinary GIP..
Who it may be relevant to
Registry conditions: Coeliac Disease. Basic parameters: 2 years — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The main reason for insufficient control of celiac disease is non-adherence to the gluten-free diet (GFD), whether voluntary or involuntary. In children, involuntary exposures are common (canteens, snacks, restaurants). There are no evidence-based recommendations regarding the best way to follow up with patients and assess adherence to the diet. Monitoring of celiac disease is traditionally based on IgA anti-transglutaminase (IgA anti-tTG) serology, but it reflects a delayed immune response and does not detect occasional exposures. Numerous studies conducted outside of France seem to highlight the usefulness of measuring gluten immunogenic peptides (GIP), compared to the current tools used. Measuring GIP in urine, which is non-invasive and can be performed regularly, could allow for earlier and more objective detection of recent gluten exposure, particularly inadvertent exposure, even before symptoms appear. Furthermore, it could serve as a complementary test for patients who continue to show symptoms or positive serology despite a reported well-followed GFD. In such situations, the use of control esophagogastroduodenoscopy (EGD) with jejunal biopsies could be reconsidered in the event of positive urinary GIP. This is the first study conducted in France on the usefulness of urinary measurement of immunogenic gluten peptides in the follow-up of pediatric celiac patients.

Interventions

  • Diagnostic test Urinary measurement of GIP
    The test used is the iVYCHECK GIP urine® test, a rapid immunochromatographic test used to detect immunogenic gluten peptides (GIP) in urine. In the experimental group, urinary GIP levels are measured at M0, M6, and M12 with two urine samples collected at home at M6 and two urine samples collected at home at M12 in addition to the sample collected during the consultation.
  • Diagnostic test Usual follow-up and measurement of urinary GIP.
    The test used is the iVYCHECK GIP urine® test, a rapid immunochromatographic test used to detect immunogenic gluten peptides (GIP) in urine. In the control group, standard follow-up at M0, M6. At M12, two urine samples collected at home in addition to the sample collected during the consultation.

Primary outcome measures

  • Compare the 1-year effectiveness of a clinical follow-up strategy based on urinary GIP measurement versus standard care, in patients with celiac disease in the pediatric population. [Time frame: 12 month]
Secondary outcome measures (4)
  • Correlation between urinary GIP concentration and presence of gastrointestinal symptoms [Time frame: Month 0 (baseline), Month 6, and Month 12 in the experimental group; Month 12 in the control group.]
  • Correlation between urinary GIP test results and pediatrician assessment of gluten intake [Time frame: Month 0 (baseline), Month 6, and Month 12 in the experimental group; Month 12 in the control group.]
  • Correlation between urinary GIP test results and anti-transglutaminase antibody serology [Time frame: Month 0 (baseline), Month 6, and Month 12 in the experimental group; Month 12 in the control group.]
  • Assess the satisfaction of patients and parents regarding the integration of the GIP into the therapeutic follow-up strategy for adherence to the RSG [Time frame: Month 12]

Eligibility criteria

Inclusion criteria

  • Children aged 2 to 18 years.
  • Confirmed diagnosis of celiac disease according to ESPGHAN criteria.
  • Gluten-free diet followed for ≥ 6 months.
  • Signed informed consent by one of the 2 parents or the legal guardian and oral or written assent from the child.
  • Affiliation to a social security scheme

Exclusion criteria

  • Predictable compliance problem in the study
  • Non-French-speaking patient
  • Seronegative celiac disease at diagnosis
  • Chronic kidney disease
  • Patient protected by law, that is, subject to protective measures (judicial safeguard, guardianship, trusteeship, procedures for opening guardianship and trusteeship measures)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

France · 1 center
  • Fondation Lenval Hôpitaux pédiatrique Nice CHU Lenval — Nice

Identifiers

NCT: NCT07578038 · 25-HPNCL-11 GIped · 2026-A00599-42

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗