NCT00140933终止3 期
A Randomized, Double-Blind, 7-Day Study of the Efficacy and Safety of Rofecoxib Versus Placebo and Diclofenac in Patients With Acute Painful Rotator Cuff Syndrome
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 274
- 试验地点
- 2
- 主要终点
- Pain during daily activities assessed by a Numerical Rating Score (NRS)
研究概览
简要总结
Comparing the short-term efficacy of rofecoxib versus placebo. Patients receive rofecoxib or placebo or diclofenac and fill out a patient diary on daytime pain severity during daily activities, night pain severity, and acetaminophen/paracetamol intake.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double
入排标准
- 年龄范围
- 18 Years 至 59 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males or females between the ages of 18 and 59 with acute painful rotator cuff syndrome.
排除标准
- 未提供
结局指标
主要结局
Pain during daily activities assessed by a Numerical Rating Score (NRS)
次要结局
- Functional impairment evaluated using Neer's functional index.
- Global assessment of disease activity by the patient with a NRS.
- Intensity of night pain evaluated by NRS.
- Rescue treatment take during the study duration.
研究者
研究点 (2)
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