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临床试验/EUCTR2006-003607-40-NL
EUCTR2006-003607-40-NL进行中(未招募)不适用

A CONTROLLED, RANDOMISED, DOUBLE-BLIND, MULTICENTER STUDY, COMPARING METHOTREXATE VS PLACEBO IN STEROID-REFRACTORY ULCERATIVE COLITIS - METEOR

Besancon University Hospital0 个研究点目标入组 110 人开始时间: 2008年8月13日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
110

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

性别
All

入选标准

  • - Between 18 and 75 years of age.
  • - UC diagnosed according to the Lennard-Jones criteria (Appendix 1) with endoscopic colorectal lesions, whatever their extension may be.
  • - A Mayo Disease Activity Index ? 4, with no item >1 for the clinical part of the score and from 0 to 2 for the endoscopic part at the time of inclusion.
  • - Steroid-dependence defined by at least 1 unsuccessful attempt to stop systemic steroid therapy during the last 12 weeks. (cf. ECCO Consensus for Crohn). Steroid therapy might have been completely stopped if it has been restarted within the last 30 days.
  • - To be receiving a treatment of prednisone at a dose between 10 and 40mg, stable for at least 2 weeks at the time of inclusion.
  • - Under an adequate contraception for male or female subjects of childbearing potential: barrier methods of contraception (condom, female condom, diaphragm, spermicidal gel) and oral contraception started at least 15 days before inclusion. This contraception will be continued throughout the study duration and at least 3 months after study termination.
  • 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) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Indication to a colectomy.
  • - Pregnant or breast-feeding female subjects.
  • - No efficacious contraception.
  • - NSAIDS or cotrimoxazole intake upon inclusion, or probenecide intake within 1 month prior to inclusion.
  • - Anti-TNF? treatment within 2 months prior to inclusion.
  • - Azathioprine, mercaptopurine, cyclosporin or thalidomide within 1 month prior to inclusion.
  • - Modification of mesalazine or olsalazine dosage within 1 month prior to inclusion.
  • - Chronic (broncho) pneumopathy.
  • - Renal failure (creatininaemia > upper limit of normal laboratory values limit).
  • - Liver disease apart from primary sclerosing cholangitis.
  • - Unexplained rise higher than twice the normal level for transaminases, alkaline phosphatases and/or bilirubin.
  • - Folate level < normal level.
  • - Infection by HIV, HBV (except in case of positive antibodies anti-HBs), HCV with serologies not older than 3 months.
  • - Past history of malignant condition (including leukaemia, lymphoma and myelodysplasia) except for baso-cellular cutaneous cancers.
  • - Obesity (BMI>30).

研究者

发起方
Besancon University Hospital

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