Natural history and clinical features of celiac disease and related non-celiac enteropathies
Official title: NATURCEL Registry: Study of the NATURal History, Epidemiological, Clinical, Diagnostic and Therapeutic Aspects of CELiac Disease and Non-celiac Enteropathies
Run by Hospital Mutua de Terrassa · NCT07070596 · Data updated 2026-11-12
This registry collects medical, genetic, and test information from people diagnosed with celiac disease or having tests for it to learn how the condition develops and is treated.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Hospital Mutua de Terrassa Academic / other |
| Locations | 1 site (Terrassa, Barcelona) |
| Status | Recruiting |
| Started | June 1, 2025 |
| Main results expected | January 1, 2030 |
| Study ends | January 1, 2030 |
| Registry record updated | July 17, 2025 |
| Trial ID | NCT07070596 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are people of any age who have been diagnosed with celiac disease or who are currently undergoing testing for celiac disease and can provide informed consent.
✕Probably not a fit
People without celiac disease or those expecting immediate treatment changes are unlikely to receive direct clinical benefit from participating in this registry.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational registry that gathers epidemiological, clinical, genetic, immunological, and diagnostic data from individuals with celiac disease and related non-celiac enteropathies. It includes people who have been diagnosed and those currently undergoing diagnostic work-up, and uses standardized data collection across participating hospitals. No experimental treatments are given; the project compiles real-world information to support scientific and translational research. Data will be used to describe disease natural history, identify clinical patterns, and support future studies.
Why it matters
Potential benefit: If successful, the registry could help improve diagnosis timing, clarify risk factors, and inform better personalized care strategies for people with celiac disease.
How similar studies have gone: Other celiac disease cohorts and registries have successfully identified genetic and clinical patterns, so using a centralized observational registry is an established approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Individuals under diagnostic evaluation for celiac disease Exclusion Criteria: * Failure to sign informed consent
Where it's running
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Hospital Universitari MútuaTerrassa
Terrassa, Barcelona, Spain Recruiting
Study contacts
- Study coordinator: Albert Martín-Cardona, MD
- Email: malaltiaceliaca@mutuaterrassa.cat
- Phone: (0034)937365050
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.