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临床试验/NCT03302442
NCT03302442已完成不适用

Comparison of Oral Molecules Preventing Relapses in Multiple Sclerosis

Nantes University Hospital1 个研究点 分布在 1 个国家目标入组 3,000 人开始时间: 2017年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
3,000
试验地点
1
主要终点
Relapse within first year of treatment

研究概览

简要总结

The aim of this observational study is to compare Dimethyl fumarate (DMF) and Teriflunomide on both clinical and MRI outcomes in patients with relapsing-remitting multiple sclerosis (RRMS) from French Observatory of Multiple Sclerosis (French MS cohort )

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • RRMS Patients with an EDSS score ranging between 0 and 5.5, who initiated either DMF or Teriflunomide before 1/01/2016 and with an available MRI scan and EDSS assessment respectively within 12 and 6 months before treatment initiation Patients who had consent to OFSEP registry Naive patient or treated with prior first line treatment : interferon, glatiramer acetate

排除标准

  • Patient with progressive multiple sclerosis
  • Patients with prior second line Patient with no MRI or EDSS score within the year before DMF or Teriflunomide initiation.

结局指标

主要结局

Relapse within first year of treatment

时间窗: 12 months

Proportion of patients experimenting at least one relapse within the first year of treatment

次要结局

  • Occurrence of clinical event at Two years(24 months)
  • Progression of disability(12 months and 24 months)
  • Radiological disease activity(12 months and 24 months)
  • Adverse drug reaction(12 months and 24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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