跳至主要内容
临床试验/EUCTR2008-005688-32-CZ
EUCTR2008-005688-32-CZ进行中(未招募)1 期

Biological therapy in the prevention of Crohn`s disease recurrence after resection in ileocecal region.

niveristy Hospital Na Bulovce0 个研究点目标入组 50 人开始时间: 2009年1月5日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • - Suitable patients for the study are all patients admitted for surgery due to ileocecal Crohn's disease, who have never been treated by any biological therapy (naive)
  • - age 18-65years
  • - no signs of system infection (viral hepatitis)
  • - negative chest X-ray and Quantiferron test for TBC
  • - no signs of heart failure
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - psychical inability to uderstand the instructions and signing of the informed consent
  • - pregnant or lactating females, or females who intend to get pregnant within 1 year
  • - patients with known allergy to Infliximab
  • - residual bowel disease (except perianal form) or after multiple resections, strictureplasty or with ostomy
  • - used biological therapy before
  • - signs of viral hepatitis
  • Further exclusion criteria
  • - adverse events after study medication
  • - patients with postoperative complications prolonging hospitalization for more than 2 weeks
  • - different perioperative finding - residual bowel disease (except perianal form)
  • - different surgical procedure (stricturoplasty, ostomy)
  • - protocol failure
  • - patient refuses further participation in the study
  • - findings of malignancy
  • The criteria of premature termination of prophylaxis
  • - signs of recurrence of Crohn's disease (increase CDAI of 75pts, endoscopic score >2, need of reoperation)

研究者

发起方
niveristy Hospital Na Bulovce

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