Natural history and clinical features of celiac disease and related non-celiac enteropathies
NATURCEL Registry: Study of the NATURal History, Epidemiological, Clinical, Diagnostic and Therapeutic Aspects of CELiac Disease and Non-celiac Enteropathies
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 |
|---|---|
| Enrollment | 1000 (estimated) |
| Sex | All |
| Sponsor | Hospital Mutua de Terrassa Academic / other |
| Locations | 1 site (Terrassa, Barcelona) |
| Trial ID | NCT07070596 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
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.
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 performed: Other celiac disease cohorts and registries have successfully identified genetic and clinical patterns, so using a centralized observational registry is an established approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Individuals under diagnostic evaluation for celiac disease Exclusion Criteria: * Failure to sign informed consent
Where this trial is running
Terrassa, Barcelona
- Hospital Universitari MútuaTerrassa — Terrassa, Barcelona, Spain (Recruiting)
Study contacts
- Study coordinator: Albert Martín-Cardona, MD
- Email: malaltiaceliaca@mutuaterrassa.cat
- Phone: (0034)937365050
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.