跳至主要内容
临床试验/NCT00725478
NCT00725478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 Parkinson Clinic Ambulances and Larger Private Practices.

Desitin Arzneimittel GmbH0 个研究点目标入组 250 人开始时间: 2008年1月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
250
主要终点
to monitor use in real practice including adverse events on piribedil

研究概览

简要总结

The aim of the non-interventional Post Marketing 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. Tolerability and course of the disease or change of parkinsonian symptoms during stabilisation on, or change over from other dopamine agonists will be documented under routine conditions. Piribedil should be prescribed according to its marketing authorisation by the responsible neurologist.

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) and/or in combination with other antiparkinsonian drugs.

排除标准

  • 未提供

结局指标

主要结局

to monitor use in real practice including adverse events on piribedil

时间窗: 3 months

次要结局

  • Efficacy(3 months)

研究者

申办方类型
Industry

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