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Analysis of Bile Acid Receptor Expression in Paraffin-Embedded Surgical Specimens from Patients with Inflammatory Bowel Disease

Analysis of Bile Acid Receptor Expression in Paraffin-Embedded Surgical Specimens from Patients with Inflammatory Bowel Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116477
Enrollment
Unknown
Registered
2026-01-11
Start date
2025-08-01
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory bowel disease

Interventions

adjacent normal intestine:None
inflamed intestinal tissue:None

Sponsors

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients clinically diagnosed with IBD, including Crohn’s disease or ulcerative colitis; 2.Patients who have undergone surgical resection of diseased intestinal segments at our hospital, with complete surgical pathology specimens available; 3.Specimens in which areas of active inflammation can be clearly distinguished from relatively normal or peri-inflammatory intestinal segments; 4.Specimens with good preservation quality and suitable for immunohistochemistry or immunofluorescence analysis; 5.Complete clinical data available for the patient, including age, sex, medical history, medication history, pathological diagnosis, and other key information;

Exclusion criteria

Exclusion criteria: 1.Specimens obtained from non-IBD patients (e.g., those with tumors, infectious colitis, etc.); 2.Tissue specimens lacking complete pathological information or with severely damaged tissue architecture, making effective staining and analysis impossible; 3.Specimens lacking clearly defined areas of active inflammation or corresponding control regions, making comparative analysis unfeasible; 4.Patients with severe comorbidities (e.g., other autoimmune diseases, primary hepatobiliary disorders) that may interfere with the assessment of bile acid metabolism or receptor expression; 5.Inability to obtain key clinical information from the patient, or cases with severely incomplete clinical data;

Design outcomes

Primary

MeasureTime frame
H-score or fluorescence intensity of intestinal tissue;

Countries

China

Contacts

Public ContactRenke Yu

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University

18768117221@163.com+86 571 8609 0073

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026