NCT00533403已完成2 期
MK0686 in Postsurgery Dental Pain (0686-002)
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 114
研究概览
简要总结
To compare the pain relieving effect of MK0686 to placebo or ibuprofen after dental surgery.
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 45 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men and women ages 18-45 years who are scheduled to have 2 or more third molars (wisdom teeth) removed
- •Patients must agree to remain in the clinic for 24 hours after surgery
排除标准
- •Patient has history of heart disease, asthma, pulmonary disease
- •Patient must discontinue use of certain pain medicines 24-72 hours prior to the surgery
研究者
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