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Multi omics study based on microbiota host interaction reveals the pathogenesis of inflammatory bowel disease associated intestinal fibrosis

The role of gut microbiota and its metabolites in the diagnosis and treatment of inflammatory bowel disease: A long-term prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097326
Enrollment
Unknown
Registered
2025-02-17
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Inflamatory bowel disease

Interventions

Cases group:None

Sponsors

Southern Medical University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign an informed consent form. 2. Age >=18 (in principle, not subject to self-modification). 3. Patients diagnosed with inflammatory bowel disease based on the internationally recognized Lennard-Jones standard.

Exclusion criteria

Exclusion criteria: 1. Have systemic diseases involving other organs, including severe diseases of important organs such as the heart, lungs, kidneys, immune-mediated disorders, metabolic diseases (e.g., diabetes, thyroid disorders), or malignant tumors. 2. Tested positive for antibodies against hepatitis C virus (HCV), human immunodeficiency virus (HIV), or syphilis during the screening period. 3. Significant laboratory abnormalities, as determined by the investigator, that may compromise patient safety or prevent completion of the clinical study: 1) Renal function: creatinine >1.5 times the upper limit of normal (ULN);2) Chronic liver disease and/or liver dysfunction: defined as AST >=1.5 times the upper limit of normal (ULN), and/or ALT >= 1.5 times the ULN, and/or total bilirubin >= 1.5 times the ULN. 4. Have other psychiatric disorders, excluding depression or anxiety disorders. 5. Have a history of substance abuse or alcohol abuse. 6. Pregnant or breastfeeding women. 7. Have severe psychological or behavioral issues that prevent cooperation with the study process or may interfere with the study. 8. Have participated in any clinical trial within the 3 months prior to signing the informed consent form. 9. The investigator deems the participant unsuitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Fecal microbiota of patients with inflammatory bowel disease before and after treatment.;Fecal microbiota metabolites of patients with inflammatory bowel disease before and after treatment.;Plasma metabolites of patients with inflammatory bowel disease before and after treatment.;Intestine tissue transcriptome of patients with inflammatory bowel disease before and after treatment.;

Countries

China

Contacts

Public ContactYe Chen

Southern Medical University Shenzhen Hospital

yechen_fimmu@163.com+86 139 2229 3223

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026