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Exploration of Efficacy Prediction and Mechanisms of Loss of Response to Infliximab in Crohn's Disease

Exploration of Efficacy Prediction and Mechanisms of Loss of Response to Infliximab in Crohn's Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122035
Enrollment
Unknown
Registered
2026-04-08
Start date
2026-04-15
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Crohn's Disease

Interventions

Observation Group of the Effect of Infliximab in Treating Crohn's Disease:None

Sponsors

The Second Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. Diagnosed with Crohn's disease (according to Chinese guidelines); 3. First use of infliximab (IFX) for the treatment of active ulcerative colitis (UC); 4. Has baseline and endpoint assessment data, or has experienced a clear failure of treatment; 5. Complete IFX administration information is available.

Exclusion criteria

Exclusion criteria: 1. IFX is used for non-active cavity-type CD indications (such as isolated perianal lesions, postoperative prevention); 2. Has previously used any biologic agents or JAK inhibitors; 3. Interrupted induction therapy due to non-efficacy reasons (such as infection, adverse reactions, compliance); 4. There is a serious lack of key baseline data; 5. The outcome cannot be clearly attributed to the insufficient efficacy of IFX.

Design outcomes

Primary

MeasureTime frame
Clinical response rate;Primary non-response rate;

Secondary

MeasureTime frame
Endoscopic response rate;CRP normalization rate;

Countries

China

Contacts

Public ContactBaisui Feng

The Second Affiliated Hospital of Zhengzhou University

zmh120338@163.com+86 371 6362 0519

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026