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临床试验/NL-OMON36084
NL-OMON36084已完成不适用

Vitamin D status and cognitive functioning in patients with relapsing remitting multiple sclerosis * a neuropsychological and functional MRI approach - Vitamin D status and cognition in MS

Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - A definite, MRI-confirmed, RRMS (Polman et al., 2005);
  • - A disease duration since the onset of first symptoms of *5 years;
  • - An age of 18-50 years;
  • - Treatment with either IFN-beta (Avonex, Betaferon, Rebif) or Glatiramer Acetate (Copaxone) or no disease modulating drugs (DMD) treatment;
  • - No exacerbation within 6 weeks prior to assessment;
  • - Vitamin D supplementation <<=20 *g/d (800 IU/d);
  • - A serum 25-hydroxyvitamin D (25(OH)D) level available within 1 year prior to inclusion, being either <50 nmol/L OR >100 nmol/L.

排除标准

  • - Progressive disease without relapses;
  • - Treatment with any immune suppressive or immune modulating drug or than IFN-beta or Glatiramer Acetate within 3 months prior to assessment;
  • - Cognitive dysfunction reported by spouses, family or MS nurses, neurologist or reported by previous neuropsychological research
  • - Presence of a depression as detected with the HADS (depression score *8;
  • - Vitamin D supplementation more than 20 *g/d (800 IU/d);
  • - Severe visual and/or verbal limitations interfering with neuropsychological testing;
  • - Contraindications for MRI examination.

研究者

发起方
Medisch Universitair Ziekenhuis Maastricht

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