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临床试验/NCT02215798
NCT02215798已完成不适用

Post-Marketing Surveillance Study on the Safety and Efficacy of Cymbalta (Duloxetine) on Diabetic Peripheral Neuropathic Pain Among Filipino Patients

Boehringer Ingelheim0 个研究点目标入组 269 人开始时间: 2006年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
269
主要终点
Frequency of serious and non-serious adverse events

研究概览

简要总结

Primary objective: To estimate the frequency of adverse events, serious and non-serious in Filipino patients with diabetic peripheral neuropathic pain treated with duloxetine 60mg once daily within the study duration of approximately 6-8 weeks in a naturalistic clinical setting. Secondary objective: To evaluate the change from baseline to endpoint in the Brief Pain Inventory (BPI) and Neuropathic Pain Questionnaire (NPQ) assessed by the investigators in duloxetine use in the treatment of diabetic peripheral neuropathic pain among Filipino patients within the study duration of approximately 6-8 weeks in a naturalistic clinical setting.

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Cymbalta

干预措施: Cymbalta (Drug)

结局指标

主要结局

Frequency of serious and non-serious adverse events

时间窗: up to 8 weeks

次要结局

  • Change from baseline in Brief Pain Inventory (BPI)(up to 8 weeks)
  • Change from baseline in Neuropathic Pain Questionnaire (NPQ)(up to 8 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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