Observational Study on the Patients With Pain Medications
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,636
- 主要终点
- To describe effective use of pain medications, describe demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment in Taiwan
研究概览
简要总结
The purpose of this study is to describe the use of pain treatments in Taiwan, the demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment.
详细描述
This is a Phase IV, multi-center, observational study to describe the use of pain treatments, the demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment. The study is conducted in an effort to understand the status of pain control in Taiwan. Currently in Taiwan, there is no approved documentation showing the most effective standard medication for treatment of patients in pain. Observational study with no study medication administered.
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
- •Outpatients only
- •Patients must have pain, previously treated with and without medication and have a VAS (Visual analogue scale) score recorded at the enrolment time
- •Patient must have a VAS score >4
排除标准
- •Patients who are receiving any investigational drug during the study
- •Patients with known or suspected psychotic disease or mental retardation.
结局指标
主要结局
To describe effective use of pain medications, describe demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment in Taiwan
时间窗: 60 days
次要结局
- Pain Relief Rating Scale(60 days)
- Global Assessments (Patient/Investigator)(60 days)
- Sleeping quality Assessment(60 days)