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Construction of database, standardization of multi-disciplinary decision making and pre linear research in application of inflammatory bowel disease

Construction of database, standardization of multi-disciplinary decision making and pre linear research in application of inflammatory bowel disease : -

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076774
Enrollment
Unknown
Registered
2023-10-18
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

inflammatory bowel disease

Interventions

MDT decision-making group:MDT decision-making
Non-MDT decision-making group:Non-MDT decision-making
Retrospective section: IBD patients:NA

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Retrospective study inclusion criteria: (1) According to the Consensus on Diagnosis and Treatment of Inflammatory Bowel Disease in China (2018, Beijing), patients clinically diagnosed with UC or CD (2) capable of independently signing an informed consent form (3) aged between 18-80 years, regardless of gender. Inclusion criteria for the randomized controlled part :(1) According to the Chinese consensus Opinion on the Diagnosis and Treatment of inflammatory bowel Disease (2018 · Beijing) (" Consensus "), patients with clinical diagnosis of CD :(2) aged 16-80 years, male or female; (3) Consistent with the diagnosis of intestinal stenosis :a. The presence of definite clinical manifestations of intestinal obstruction without neoplastic stenosis; B-imaging, ultrasound or endoscopy: intestinal ultrasound /CT to measure intestinal wall thickness > 4mm, and the diameter of the stenosed upper segment of the bowel > 3cm; The simplified endoscopy for Crohn's disease (SES-CD) score was "stenosis"; The colonoscopy could not pass through; c Pathology: surgical pathology suggested submucosal and/or lamina propria fibrosis: or biopsy pathology could fully observe submucosa, there was submucosal fibrosis.

Exclusion criteria

Exclusion criteria: (1) Failure to provide informed consent (2) Simultaneous presence of additional autoimmune disorders or malignant tumors within the gastrointestinal system. Exclusion criteria for the control group: a. Failure to provide informed consent. b. Coexistence of other autoimmune diseases or gastrointestinal malignancies. c. Pregnant individuals or those with contraindications for intestinal surgery. Inclusion criteria for the randomized controlled part :(1) Refusal to sign informed consent :(2) pregnant women with other autoimmune diseases or malignant tumors of the digestive tract :(3) inappropriate use of biological agents or surgery; (4) refusing to attend the consultation of enteropathy in Peking Union Medical College Hospital.

Design outcomes

Primary

MeasureTime frame
Success rate of treatment at 12 months after treatment;

Secondary

MeasureTime frame
Proportion of major clinical events among patients;

Countries

China

Contacts

Public ContactHong Yang

Peking Union Medical College Hospital

hongy72@163.com+86 186 1011 0325

Outcome results

None listed

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