跳至主要内容
临床试验/NL-OMON41844
NL-OMON41844已完成不适用

REAL_PD - REAL_PD

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 20 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
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational non invasive

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Dutch Parkinson patients
  • - Male or female
  • - Age 30 years or older at time of PD diagnosis
  • - Subjects must have at least two of the following: resting tremor, bradykinesia, rigidity (must have either resting tremor or bradykinesia); OR either asymmetric resting tremor or asymmetric bradykinesia
  • - Ability to provide written informed consent in accordance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and local regulations

排除标准

  • - Little or no response to adequate doses of levodopa or a dopamine agonist
  • - Atypical PD syndromes due to either drugs (e.g., metoclopramide, flunarizine, neuroleptics) or metabolic disorders (e.g., Wilson*s disease), encephalitis, or degenerative diseases (e.g., progressive supranuclear palsy)
  • - A clinical diagnosis of dementia as determined by the investigator
  • - Any other medical or psychiatric condition or lab abnormality, which in the opinion of the investigator might preclude participation
  • - Previously obtained CT MRI scan is suggestive of another cause of parkinsonism, or with evidence of clinically significant other neurological disorder (in the opinion of the investigator)

研究者

发起方
niversitair Medisch Centrum Sint Radboud

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