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
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