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Multi-omics exploration of gut microbiome-host co-metabolic characteristics in inflammatory bowel disease with metabolic dysfunction-associated steatotic liver disease

Multi-omics exploration of gut microbiome-host co-metabolic characteristics in inflammatory bowel disease with metabolic dysfunction-associated steatotic liver disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117390
Enrollment
Unknown
Registered
2026-01-23
Start date
2025-10-20
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Inflammatory bowel disease-metabolic dysfunction-associated steatotic liver disease(IBD-MASLD)

Interventions

IBD-non-MASLD group:None
IBD-MASLD group:None

Sponsors

Longhua Hospital Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: From October 2025 to October 2027, patients diagnosed with IBD in the gastroenterology department of the research unit.

Exclusion criteria

Exclusion criteria: 1. Excessive alcohol consumption (ethanol intake >=210 g/week for men and >=140 g/week for women); 2. Colitis due to other causes, including infectious enteritis (e.g., bacterial, amoebic, or schistosomal), drug-induced enteropathy, or radiation-induced colitis; 3. Steatotic liver disease attributable to other etiologies, including genotype 3 HCV infection, drug-induced steatosis, Wilson's disease, or malnutrition; 4. Hematologic disorders unsuitable for blood sampling; 5. Pregnancy (confirmed by serum ß-hCG testing), lactation, or women actively planning pregnancy; 6. Use of medications known to affect hematologic parameters or gut microbiota within one month prior to enrollment; 7. Pre-existing primary diseases of vital organs (heart, liver, kidney) or other severe conditions deemed by investigators to contraindicate participation; 8. Age <18 years, or lack/limitation of legal capacity.

Design outcomes

Primary

MeasureTime frame
Controlled Attenuation Parameter;Liver Stiffness Measurement ;

Secondary

MeasureTime frame
General clinical data;Improved version of Mayo score;PRO questionnaire scoring scale;Metabolic risk assessment;

Countries

China

Contacts

Public ContactXu Hanchen

Longhua Hospital Shanghai University of Traditional Chinese Medicine

hanson0702@126.com+86 189 1776 3576

Outcome results

None listed

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