Prospective Cohort Establishment and Clinical Observation of Children With Crohn's Disease
Condition(s) studied
Investigational drug(s) / intervention(s)
enteral nutrition: exclusive enteral nutrition therapy or Partial enteral nutrition
Immunotherapy: Immunosuppressants therapy, Including thalidomide, azathioprine, methotrexate, etc
biological agents: Inflixima , domestic infliximab (Taizhou Mabtech Pharmaceutical Co.,Ltd) and Adalimumab , etc
Glucocorticoids: Glucocorticoids treatments are given
fecal microbiota transplantation: Fecal bacteria transplantation treatment, transplantation routes include enema, TET route, capsule fecal bacteria route, etc
Study summary
To evaluate the clinical manifestations, treatment options, and improved clinical outcomeof children with Crohn's disease in real-world Settings: (1) analysis of clinical manifestations; (2) probability of using the same treatment options; (3) Clinical outcome;
Eligibility
Primary outcome measure(s)
- To evaluate the clinical manifestations, treatment options, and clinical outcomes of Crohn's disease in children in real-world Settings — 14 weeks
14 weeks clinical response rate.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Tongji Hospital, Wuhan, 430030 | Wuhan | China |
More Tongji Hospital trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06673134 on ClinicalTrials.gov ↗ ← All trials in China