跳至主要内容
临床试验/CTRI/2018/02/011948
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

发起方
ovartis India Limited

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