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临床试验/EUCTR2014-004650-34-IT
EUCTR2014-004650-34-IT进行中(未招募)1 期

euromodulation strategies to enhance the effects of gait rehabilitation in multiple sclerosis patients with cerebellar ataxia - New strategies in neurological diseases

IRCCS FONDAZIONE ISTITUTO NEUROLOGICO NAZIONALE C. MONDINO0 个研究点目标入组 45 人开始时间: 2020年11月5日最近更新:
适应症
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
45

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

  • Aged 18–70 years,
  • With clinically defined multiple sclerosis (McDonald 2010),
  • Able to complete two trials of the timed 25-foot walk (T25FW)
  • EDSS between 4 and 6,
  • International Cooperative Ataxia Rating Scale (ICARS) walking capacities score =2,
  • Pyramidal Functional System Score (FSS) =2.
  • 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 30
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 15

排除标准

  • Onset of multiple sclerosis exacerbation within 90 days of screening,
  • A history of seizures a history of seizures or the presence of vascular, infectious or methabolic lesions of the cerebral cortex leading to symptomatic seizures,
  • Allergy to pyridine or tablet excipients
  • Patients treated with drugs containing 4-aminopyridine,
  • Any condition that would interfere with the conduct or interpretation of the study,
  • Contraindication to the use of the Transcranial Magnetic Stimulator,
  • Clinically significant abnormal laboratory values or electrocardiogram at screening,
  • Patients with impaired renal function mild, moderate or severe (creatinine cleareance <80 ml/min),
  • Patients treated with OCT2 inhibitors, for example cimetidine,
  • Women were excluded if they were pregnant, lactating or of childbearing potential and not using adequate birth control.
  • We set additional restrictions on changes in concomitant medications to avoid related changes in multiple sclerosis symptoms during the trial.

研究者

发起方
IRCCS FONDAZIONE ISTITUTO NEUROLOGICO NAZIONALE C. MONDINO

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