跳至主要内容
临床试验/NCT00727727
NCT00727727已完成不适用

Stabilization on, or Change-Over to the Non-Ergot Dopamine Agonist Piribedil in Patients With Morbus Parkinson - a Post Marketing Surveillance Study in Private Practices.

Desitin Arzneimittel GmbH1 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2008年3月最近更新:
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
750
试验地点
1
主要终点
to monitor use in daily routine practice including adverse events

研究概览

简要总结

The objective of the Post Marketing Surveillance Study is to investigate the use of the non-ergot dopamine agonist piribedil (trade name: CLARIUM) in mono- and combination therapy in patients with Morbus Parkinson. Neurologists in private practices in Germany should document the safety and course of the disease/change of parkinsonian symptoms during stabilisation on, or change over from other dopamine agonist treatment under routine conditions. Piribedil should be prescribed according to its marketing authorisation.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female patients 18 years and older.
  • Indication: Morbus Parkinson.
  • Treatment with piribedil for the first time.
  • Monotherapy with piribedil.
  • Combination therapy with L-Dopa (from the beginning or secondary in combination with other antiparkinsonian drugs).

排除标准

  • 未提供

研究组 & 干预措施

Parkinsonian patients

干预措施: Piribedil (Drug)

结局指标

主要结局

to monitor use in daily routine practice including adverse events

时间窗: 3 months

次要结局

  • to monitor use in daily routine practice including efficacy aspects(3 months)

研究者

申办方类型
Industry

研究点 (1)

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