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