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临床试验/EUCTR2013-000337-13-DE
EUCTR2013-000337-13-DE进行中(未招募)1 期

Prediction of response to Certolizumab Pegol treatment by functional MRI of the brain. A multi-center, randomized double-blind controlled studyPrediction of response to Certolizumab-Pegol in RA (PreCePRA)

niversitätsklinikum Erlangen0 个研究点目标入组 156 人开始时间: 2013年2月12日最近更新:
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
156

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

  • Understands and voluntarily signs an informed consent
  • Male or female, aged = 18 years at time of consent
  • Must be able to adhere to the study visit schedule and
  • other protocol requirements
  • Must satisfy the 2010 ACR/EULAR classification criteria
  • for rheumatoid arthritis plus a disease duration of at
  • least 6 months
  • Must have active RA with a DAS28 =3.2
  • = 3 swollen and/or tender joints of the hands
  • At screening- visit patients should have been treated
  • without alterations of therapy for at least three months
  • with DMARDS (i.e. Methotrexate) with or without
  • concomitant use of steroids).
  • Glucocorticoids treatment up to 10mg prednisolone per
  • day will be allowed at study entry.
  • 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 156
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Individuals not able to understand and follow study
  • protocol and not able to voluntarily sign informed consent
  • Individuals with claustrophobia, tattoos containing metal,
  • magnetic endoprostheses, surgery on bone in between a
  • time interval < 3 months.
  • Patients treated before with any biological or small
  • molecule or medication under investigation for the
  • treatment of RA.
  • Patients with serious or chronic infections within the
  • previous 3 months
  • Opportunistic infections within the 6 months before
  • Cancer within the 5 years before screening (with the
  • exception of treated and cured squamous or basal cell
  • carcinoma of the skin)
  • History of severe congestive heart failure
  • Current signs or symptoms of severe, progressive, or
  • uncontrolled renal, hepatic, hematologic, gastrointestinal
  • (a.e.diverticulitis), endocrine, pulmonary, cardiac,
  • neurologic or cerebral disease
  • Transplanted organ (with the exception of corneal
  • transplantation done more than 3 months before
  • Evidence of active tuberculosis

研究者

发起方
niversitätsklinikum Erlangen

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