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临床试验/EUCTR2010-023678-38-IT
EUCTR2010-023678-38-IT进行中(未招募)不适用

High-field structural and functional MRI to investigate the substrates of fatigue in multiple sclerosis and to monitor the effect of tailored treatments.Pharmacological substudy. - ND

FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR0 个研究点开始时间: 2011年2月2日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • -No relapses and steroid treatment in the three months preceding study initiation;
  • - No or only modest overall neurological impairment defined as an EDSS score of 4.0 or less;
  • - No visual deficits;
  • - No right upper limb impairment that may interfere with fMRI performance;
  • - No pain disturbances;
  • - No other neurological diseases;
  • - No psychiatric or mood disorders;
  • - No evidence of depression at the Montgomery and Asberg Depression Rating Scale (1979);
  • - No epilepsy, learning disability, head injury, episodes of loss of consciousness or severe ongoing stressors;
  • - No history of drug or alcohol abuse;
  • - No concomitant therapy with antidepressant, baclofen, psychoactive, and steroids drugs as well as symptomatic treatment for fatigue;
  • - For patients treated with interferons (IFN) or other immunomodulants: treatment should be started at least six months before MRI acquisition and fatigue should not be a side effect of IFN treatment;
  • - No major medical illness including renal, hepatic or cardiac disease, or diabetes mellitus.
  • - No pregnancy or breastfeeding;
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Recurrence-and steroid treatment in the three months preceding the start of the study;
  • - Even modest global neurological damage defined by EDSS scores of 4.0 or less;
  • - Visual impairment;
  • - Direct damage to the upper limbs that may interfere with fMRI;
  • - Pain disorder;
  • - Other neurological disease;
  • - Psychiatric disorder or mood;
  • - Evidence of depression and the Montgomery Asberg Depression Rating Scale (1979);
  • - Epilepsy, learning disabilities, head injury, episodes of loss of consciousness or severe stressors in progress;
  • - Previous abuse of drugs or alcohol;
  • - Concomitant treatment with antidepressants, baclofen, psychoactive drugs and steroids, as well as symptomatic treatment for fatigue;
  • - Patients treated with interferon (IFN) or other immunomodulatory treatment with recent
  • - Serious illness such as kidney disease, liver or heart, or diabetes mellitus.
  • -Pregnant or lactating;

研究者

发起方
FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR

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