跳至主要内容
临床试验/EUCTR2008-003581-26-SE
EUCTR2008-003581-26-SE进行中(未招募)不适用

Pharmacokinetics of levodopa using duodenal levodopa/carbidopa infusion with and without oral COMT inhibitors - DuoCOMT

Dept of Neuroscience, Uppsala University0 个研究点开始时间: 2008年5月30日最近更新:
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

  • Clinically diagnosed Parkinson's disease, ongoing Duodopa therapy.
  • Age 30-90 years.
  • At least 4 persons of each gender.
  • Hoehn & Yahr-stage 3-5 at worst.
  • 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

  • Ongoing treatment with COMT-inhibitor.
  • Treatment with neuroleptics (atypical neuroleptics are OK).
  • Liver disease.
  • Hypersensitivity against Comtess or Tasmar.

研究者

发起方
Dept of Neuroscience, Uppsala University

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