跳至主要内容
临床试验/EUCTR2005-005989-37-FI
EUCTR2005-005989-37-FI进行中(未招募)不适用

CogniMS: observational study to assess cognition in patients with early Multiple Sclerosis - CogniMS

Schering Oy0 个研究点目标入组 2,000 人开始时间: 2006年2月17日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
2,000

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

  • Patient selection and observation: This observational study focuses on patients with relapsing-remitting MS diagnosed within the last 2 years (according to McDonald or Poser criteria), who have started treatment with Betaferon during the last 6 months. The prescription of the medicine is clearly separated from the decision to include the patient in the study. The patients will be screened for cognitive changes, depression, HrQoL and fatigue every 6 months for 2 years. Patients are either newly recruited for CogniMS or have previously participated in the CogniCIS study until they have fulfilled diagnostic criteria for MS.
  • Are the trial subjects under 18?
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years)
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years)
  • F.1.3.1 Number of subjects for this age range

排除标准

  • See Inclusion Criteria.

研究者

发起方
Schering Oy

相似试验