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临床试验/NCT06203158
NCT06203158已完成不适用

Intestinal Epithelial Fucosylation Affects the Efficacy of Ustekinumab in Crohn's Disease

Second Affiliated Hospital of Wenzhou Medical University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年12月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
clinical remission rate at 24 week

研究概览

简要总结

The loss of response rate of ustekinumab(UST) is high, and the specific mechanism has not yet been elucidated. Molecular markers that can accurately predict the efficacy of UST are urgently needed to provide theoretical basis for guiding individualized treatment. Therefore, this study intends to explore the impact of intestinal epithelial fucosylation levels on the efficacy of UST in patients with Crohn's disease(CD), aiming to provide predictable molecular markers for UST to accurately treat CD.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with moderate to severe Crohn's disease
  • Receiving treatment with ustekinumab
  • Received colonoscopy and collected intestinal tissue samples before and after treatment

排除标准

  • Hypersensitivity to any component of ustekinumab
  • Cognitive or developmental disabilities prevent you from completing this study
  • Combined with diseases such as RA, diabetes, systemic lupus erythematosus, intestinal tuberculosis, ischemic enteritis, radiation enteritis and tumors

结局指标

主要结局

clinical remission rate at 24 week

时间窗: at 24 week

A specialist will evaluate the HBI score at 24 week based on the patient's clinical symptoms and determine whether the patient is in clinical remission based on the score.

次要结局

未报告次要终点

研究者

发起方
Second Affiliated Hospital of Wenzhou Medical University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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