跳至主要内容
临床试验/NCT00311532
NCT00311532已完成不适用

Observational Study to Determine the Incidence of New-Onset Valvulopathy in Patients Treated With Pergolide as Second-Line Therapy for Parkinson's Disease

Eli Lilly and Company1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2006年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
200
试验地点
1

研究概览

简要总结

The primary objective of this study is to estimate the incidence of new-onset valvulopathy, determined by baseline and follow-up echocardiograms, in patients with Parkinson's Disease who are receiving pergolide as second-line therapy.

The secondary objective of the study is to estimate the prevalence of valvulopathy, as determined by baseline echocardiograms, among all patients who have Parkinson's Disease and are being considered for pergolide as second-line therapy.

研究设计

研究类型
Observational
观察模型
Defined Population
时间视角
Other

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 or female, age 18 and older with a diagnosis of Parkinson's Disease
  • Receiving pergolide as second-line therapy as prescribed by Summary of Product Characteristics
  • Willing to participate and sign a consent to release medical information
  • Have had an echocardiogram within 3 months of initiation of pergolide therapy with no evidence of cardiac valvulopathy

排除标准

  • There are no exclusion criteria for this study

研究者

申办方类型
Industry

研究点 (1)

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