跳至主要内容
临床试验/NCT03839680
NCT03839680Unknown不适用

Measuring Endoscopic ACTIvity in Patients Treated With VEDOlizumab for Ulcerative Colitis

Centre Hospitalier Universitaire de Besancon4 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2018年2月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
60
试验地点
4
主要终点
Mucosal healing at defined by Mayo endoscopic sub-score ≤ 1 or UCEIS ≤ 1

研究概览

简要总结

Describe the proportion of patients with ulcerative colitis (UC) treated with vedolizumab (VDZ) who achieve mucosal healing at week 54 of treatment.

研究设计

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

入排标准

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

入选标准

  • age over 18 years,
  • established diagnosis of ulcerative colitis for at least 3 months
  • moderate to severe active ulcerative colitis with a Mayo endoscopic sub-score ≥ 1 before vedolizumab introduction
  • patients receiving vedolizumab according to French drug labelling (previous exposure to anti-TNF, contraindicated or intolerant to anti-TNF),
  • possibility of concomitant therapy including corticosteroids and immunosuppressors,
  • patients naive to anti-integrin,
  • no contraindication to proctosigmoidoscopy

排除标准

  • age under 18 years
  • ulcerative colitis not proven, Crohn's disease, or inderterminate colitis
  • personal history of high-grade dysplasia or colorectal cancer
  • surgery with ileo-anal anastomosis
  • patients' refusal to participate in the study

结局指标

主要结局

Mucosal healing at defined by Mayo endoscopic sub-score ≤ 1 or UCEIS ≤ 1

时间窗: 54 weeks

次要结局

  • Mucosal healing at defined by Mayo endoscopic sub-score 0 or UCEIS 0(54 weeks)
  • Endoscopic pattern of mucosal healing(54 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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