跳至主要内容
临床试验/NCT00605163
NCT00605163Unknown不适用

A Longitudinal Observational Follow-up of the PRECEPT Study Cohort

The Parkinson Study Group55 个研究点 分布在 2 个国家目标入组 530 人开始时间: 2006年8月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
530
试验地点
55
主要终点
Unified Parkinson Disease Rating Scale (UPDRS) and β-CIT SPECT imaging of the dopamine transporter.

研究概览

简要总结

The purpose of this study is to longitudinally follow consenting clinical trial participants who participated in PRECEPT (A Randomized, Double Blind, Placebo Controlled, Dose Finding Study to Assess the Efficacy and Safety of CEP 1347 in Patients With Early Parkinson's Disease). The study will assess the clinical and imaging outcomes relevant to the natural history of Parkinson's disease (PD), as well as determine early biomarkers of the disease.

研究设计

研究类型
Observational
观察模型
Cohort

入排标准

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

入选标准

  • Participation in the PRECEPT study
  • Willing and able to give informed consent

排除标准

  • Patients will be excluded from participating in the the study if either of the criteria stated above is not met

结局指标

主要结局

Unified Parkinson Disease Rating Scale (UPDRS) and β-CIT SPECT imaging of the dopamine transporter.

时间窗: Annual, ongoing assessments

次要结局

  • University of Pennsylvania Smell Identification Test (UPSIT)(Annual, ongoing assessments)

研究者

发起方
The Parkinson Study Group
申办方类型
Network

研究点 (55)

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