Histological and Molecular Profiling in the Diagnostics and Treatment of Small-Bowel Diseases - A Prospective Cohort Study (The DeepBowel Study)
Sponsor: Tampere University Hospital
Trial Details
| Condition | Celiac Disease, Small Bowel Disease, Refractory Celiac Disease |
| Status | Recruiting |
| Participants | 300 |
| Est. Completion | 31 Dec 2035 |
| Last Updated | 29 Apr 2026 |
Primary Outcome
Villus-to-crypt ratio; Transcriptomic
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * Age ≥ 18 years * Clinically indicated upper gastrointestinal endoscopy (gastroscopy) * Written informed consent obtained prior to procedure * For Group 1 (Healthy Controls): Negative celiac disease antibodies (anti-transglutaminase and/or anti-endomysium); no suspected celiac * For Group 2 (Celiac Diagnostics): Referred for primary celiac disease diagnostics requiring duodenal biopsy * For Group 3 (Refractory Injury): Confirmed small-bowel mucosal injury not responsive to a gluten-free diet Exclusion Criteria: * For Group 1 (Healthy Controls): Other small-bowel diseases causing mucosal injury, including Crohn's disease and small-bowel ulcers * Inability to provide written informed consent * Refusal to participate
Trial Sites
Countries
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