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Histological and Molecular Profiling in the Diagnostics and Treatment of Small-Bowel Diseases - A Prospective Cohort Study (The DeepBowel Study)

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

This prospective cohort study aims to establish reliable histological reference values for normal small-bowel mucosa, improve histological diagnostic quality in celiac disease, and develop an advanced molecular profile for disease diagnosis and treatment response evaluation. The study will collect duodenal biopsies from three groups: healthy controls undergoing clinically indicated gastroscopy, patients referred for primary celiac disease diagnostics, and patients with small-bowel mucosal injury unresponsive to a gluten-free diet. Patients will undergo routine clinical assessment via standard pathology review of diagnostic biopsies. Biopsies will be analyzed using digital morphometry, AI-based image analysis, RNA sequencing (transcriptomics), and intestinal organoid cultures.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• 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

Locations
Other Locations
Finland
Hatanpää Specialist Medical Care
RECRUITING
Tampere
Tampere University Hospital (Tays)
RECRUITING
Tampere
Valkeakoski Regional Hospital
RECRUITING
Valkeakoski
Contact Information
Primary
Juha Taavela
juha.taavela@tuni.fi
+358443400330
Time Frame
Start Date: 2025-11-01
Estimated Completion Date: 2035-12-31
Participants
Target number of participants: 300
Treatments
Group 1 - Healthy Controls (n = 130)
Adults ≥18 years undergoing clinically indicated gastroscopy (e.g., reflux symptoms) with no suspicion of celiac disease and negative celiac antibodies (anti-transglutaminase and/or anti-endomysium).
Group 2 - Celiac Disease Diagnostic Group (n = 130)
Adults referred for primary celiac disease diagnostics requiring duodenal biopsy, in accordance with standard care guidelines.
Group 3 - Refractory Small-Bowel Injury Group (n = 40)
Adults with small-bowel mucosal injury (villous atrophy) that does not respond to a gluten-free diet, referred for endoscopy to exclude ongoing histological damage.
Related Therapeutic Areas
Sponsors
Leads: Tampere University Hospital
Collaborators: Tampere University

This content was sourced from clinicaltrials.gov