NCT02248207已完成不适用
Management of Parkinson's Disease Patients at Their First Visits in a Neurological Practice
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 1,293
- 主要终点
- Global Assessment of efficacy by investigator on a 4-point scale
研究概览
简要总结
Study to obtain information about the co-operation of the different physician-colleagues in the treatment of patients with Parkinson's disease, both in private practices and clinics and about the primary treatment strategies in the pharmacotherapy of Parkinson's disease and to collect data on the tolerability of Sifrol® in ambulatory patients suffering from Parkinson's disease under routing conditions
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with Parkinson's disease who present to the specialist neurologist practice for the first time without or with referral and who are planned to receive or either be switched to Sifrol or continue the previously prescribed therapy with Sifrol® can be included in this observational study
排除标准
- •Neurologists are asked to consider the Summary of Product Characteristics (SPC) for Sifrol®
研究组 & 干预措施
Parkinson Disease patients
干预措施: Pramipexole (Drug)
结局指标
主要结局
Global Assessment of efficacy by investigator on a 4-point scale
时间窗: after 8 weeks
Change from Baseline in actual Parkinson symptoms
时间窗: Baseline, after 8 weeks
Global Assessment of tolerability by investigator on a 4-point scale
时间窗: after 8 weeks
次要结局
- Number of patients with adverse drug reactions(up to 8 weeks)
研究者
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