NCT07362654 Single-cell Immune Response to Controlled Gluten Ingestion in Pediatric Celiac Disease
| NCT ID | NCT07362654 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud |
| Condition | Celiac Disease |
| Study Type | INTERVENTIONAL |
| Enrollment | 51 participants |
| Start Date | 2025-07-07 |
| Primary Completion | 2026-04 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 51 participants in total. It began in 2025-07-07 with a primary completion date of 2026-04.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This study investigates how the immune system of children with celiac disease responds to controlled, small amounts of gluten. Children on a strict gluten-free diet are randomly assigned to receive either placebo, 50 mg of gluten, or 5 g of gluten once daily for three days, simulating real-life accidental exposure or dietary transgression. Blood samples are collected on Day 1 (before gluten intake) and Day 8 (five days after the last dose). Stool and urine samples are also collected for complementary analyses. Using single-cell ribonucleic acid (RNA) sequencing, T-cell receptor sequencing, microRNA profiling, and exploratory metabolomics, the study aims to characterize changes in immune cell populations and gene expression after gluten exposure. The objective is to determine whether even very small amounts of gluten induce measurable systemic immune responses and whether these responses differ according to the dose administered. Understanding these mechanisms may support the development of new biomarkers and improve clinical management of pediatric celiac disease.
Eligibility Criteria
Inclusion Criteria: * Age 8 to 14 years at study entry. * Diagnosis of celiac disease according to ESPGHAN 2020 criteria. * At least 18 months on a strict gluten-free diet (GFD). * Adequate adherence to the GFD, demonstrated by negative fecal gluten immunogenic peptides (GIP) prior to inclusion. * Asymptomatic from a gastrointestinal perspective in the preceding weeks. * Ability to swallow the gluten/placebo preparation. * Written informed consent from parents/legal guardians and assent from the child. Exclusion Criteria: * Obesity defined as BMI ≥ 95th percentile according to WHO criteria. * Diagnosed inflammatory bowel disease or diabetes mellitus. * Acute infectious illness at the time of inclusion. * Chronic hepatic, pulmonary, renal, or rheumatologic disease. * History of severe acute reactions to accidental gluten ingestion. * Use of oral corticosteroids or immunosuppressive therapy in the previous 3 months. * Any condition that, in the opinion of the investigators, may contraindicate participation or compromise study integrity.
Contact & Investigator
Rafael Martín Masot, MD, PhD
PRINCIPAL INVESTIGATOR
Hospital Regional Universitario de Málaga / IBIMA-BIONAND
Frequently Asked Questions
Who can join the NCT07362654 clinical trial?
This trial is open to participants of all sexes, aged 8 Years or older, up to 14 Years, studying Celiac Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07362654 currently recruiting?
Yes, NCT07362654 is actively recruiting participants. Contact the research team at rafammgr@uma.es for enrollment information.
Where is the NCT07362654 trial being conducted?
This trial is being conducted at Málaga, Spain.
Who is sponsoring the NCT07362654 clinical trial?
NCT07362654 is sponsored by Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud. The principal investigator is Rafael Martín Masot, MD, PhD at Hospital Regional Universitario de Málaga / IBIMA-BIONAND. The trial plans to enroll 51 participants.