EUCTR2004-004509-11-DE进行中（未招募）不适用
Efficiency and tolerability of L-Dopa in patients with Hereditary Spastic Paraplegia (HSP)
niversity hospital of the University of Ulm0 个研究点开始时间: 2005年9月6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
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
- •1.) patients (Females and males) aged between 18 to 80 years.
- •2.) definite noncomplicated spastic paraplegia
- •3.) ability to understanding the written patients information
- •4.) ability to cive a written consent
- •5.) normal electrocardiogramm
- •6.) females of childbearing age: use of pregnancy preventing arrangements
- •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) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1.) participation in a clinical trial in the past 12 month using other medicinical pharmaceuticals
- •2.) contraindications for a therapy with Levodopa: pregnancy, lactation period
- •3.) Use of Levodopa or dopamine agonists in the past 3 months
- •4.) any diseases in which the release of functional testing could be impaired
- •5.) noncomplained patients
- •6) therapy with phenytoine, papaverine, inhibitors of monoaminooxidase A and B, drugs containing iron sulphit
- •7) coronary heart disease and cardiac arrhythmias
- •8) pregnancy, lactation period
研究者
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