CTRI/2018/02/011948招募中4 期
A prospective, 16 week, phase IV study to evaluate safety, tolerability and effectiveness in patients with severe dementia of the Alzheimer�s type exposed to rivastigmine (Exelon)15cm2 transdermal patch
ovartis India Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1)Patients willing to participate in the study by providing written informed consent.
- •2)Patients diagnosed with severe dementia secondary to Alzheimerââ?¬•s disease (AD)
- •3)Patientââ?¬•s prescribed with rivastigmine 27mg -15 cm2 transdermal patch as per discretion of treating physician
排除标准
- •1)Contraindication as per PI
- •2)Patients simultaneously participating in other studies
研究者
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