NCT00092313已完成3 期
A Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled Study to Evaluate the Efficacy of Rofecoxib and a Dosing Regimen of Oxycodone With Acetaminophen Over 24 Hours in Patients With Postoperative Dental Pain
适应症
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 271
- 主要终点
- Post-op dental pain over 6 hours as measured by pain intensity/relief scores, patient global assessment, and time to perceptible/meaningful pain relief.
研究概览
简要总结
The purpose of this study is to compare the safety and effectiveness of two approved drugs in the treatment of pain following dental surgery.
详细描述
The duration of treatment is 24 hours.
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 (Participant, Investigator)
入排标准
- 年龄范围
- 16 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Impaction of a molar tooth requiring removal
排除标准
- •Known allergy to the study drugs
结局指标
主要结局
Post-op dental pain over 6 hours as measured by pain intensity/relief scores, patient global assessment, and time to perceptible/meaningful pain relief.
次要结局
- Time to onset of analgesic effect, peak analgesic effect, and/or duration of analgesic effect over 24 hours.
研究者
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