跳至主要内容
临床试验/NCT06639620
NCT06639620招募中不适用

Effectiveness aNd Use of fosleVOdopa-foscarbidopa in Advanced Parkinson Disease in Real Life Setting

AbbVie61 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年11月12日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
61
主要终点
Change From Baseline in Parkinson's Disease Questionnaire-8 (PDQ) total score.

研究概览

简要总结

Parkinson's disease (PD) is a neurological condition, which affects the brain. PD gets worse over time, but how quickly it progresses varies a lot from person to person. Some symptoms of PD are tremors, stiffness, and slowness of movement. This study will assess how effective foscarbidopa/ foslevodopa is in treating French adult participants with advanced Parkinson disease under routine clinical practice.

Foslevodopa/foscarbidopa is an approved drug outside of US for the treatment of Parkinson's Disease. Approximately 200 adult participants who are prescribed foslevodopa/foscarbidopa by their doctors will be enrolled across approximately 30 sites in France.

Participants will receive foscarbidopa/ foslevodopa subcutaneous infusion as prescribed by their physician. Participants will be followed for up to 12 months.

There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.

研究设计

研究类型
Observational
观察模型
Cohort
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
否

入选标准

  • •Participants with advanced Parkinson disease with motor complications insufficiently controlled by current therapy
  • •Participants eligible for foscarbidopa / foslevodopa according to French label & regulation.
  • •Treatment initiation decision prior to and independently from study enrolment

排除标准

  • •Participants with any contraindication to foscarbidopa / foslevodopa.
  • •Participants with Mini mental state examination (MMSE) score < 24

研究组 & 干预措施

Foscarbidopa / Foslevodopa

Participants will receive foscarbidopa/ foslevodopa as prescribed by their physician according to local label

结局指标

主要结局

Change From Baseline in Parkinson's Disease Questionnaire-8 (PDQ) total score.

时间窗: Up to approximately 12 months

Parkinson Disease Questionnaire (PDQ)-8 is an eight-question instrument constructed by taking one question from each domain of PDQ-39: mobility, activities of daily of living, emotional well-being, stigma, social support, cognition, communication, and bodily discomfort. Each question is scored between 0 and 4 as follows: 0=Never and 4 = Always or cannot do at all. A higher score signifies poorer quality of life.

次要结局

未报告次要终点

研究者

发起方
AbbVie
申办方类型
Industry
责任方
Sponsor

研究点 (61)

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