NCT00219232已完成3 期
An Open-label Extension to Evaluate the Efficacy and Safety of the Rivastigmine Transdermal Patch in Patients With Probable Alzheimer's Disease
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- Novartis
- 入组人数
- 868
- 主要终点
- Safety and tolerability as measured by adverse events, vital signs and skin irritation for up to 28 weeks treatment
研究概览
简要总结
The goal of this research study is to evaluate, in the open-label extension phase, the safety and efficacy of the rivastigmine transdermal patch in patients with probable Alzheimer's Disease
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 50 Years 至 85 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who fulfilled the inclusion and
排除标准
- •as listed in the study CENA713D2320 and have completed the double-blind treatment phase on study medication without significant protocol violations.
结局指标
主要结局
Safety and tolerability as measured by adverse events, vital signs and skin irritation for up to 28 weeks treatment
次要结局
- Change in activities of daily living from baseline at week 52
- Change in behavioral symptoms from baseline at week 52
- Change in executive function from baseline at week 52
- Change in cognition from baseline (week 24 of the double blind phase) at week 52
- Clinical global impression of change from baseline at week 52
研究者
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