NCT00664690撤回4 期
Effect of Celecoxib on Transitional Pain After Outpatient Surgery
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- visual analogue score for pain
研究概览
简要总结
Sixty adults having shoulder and forearm surgery will receive either placebo or celebrex started preoperatively and continued for 3 days. Rescue medications required as well as pain scores will be assessed using a patient diary to evaluate the effect of celebrex in controlling transitional pain
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
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients scheduled for elective ambulatory surgery of the shoulder
- •ASA I - III
- •Able to read English
- •Male or female
排除标准
- •Allergy to local anesthetic, Cox2, sulpha drug, acetaminophen or oxycodone
- •Women who are pregnant or lactating and women of childbearing age and not following acceptable contraceptive precautions
- •Any major medical or psychiatric problem
- •Those with a known history of narcotic dependence, abuse or chronic narcotic intake
- •Patients with known history of peptic ulcer or GI bleeding in the past, ulcers, congestive heart failure, angina or previous heart attack, coagulation problems, venous thrombosis, kidney or liver disease or strokes
研究组 & 干预措施
1
Experimental
celebrex
干预措施: celebrex (Drug)
2
Placebo Comparator
placebo
干预措施: placebo (Drug)
结局指标
主要结局
visual analogue score for pain
时间窗: post-op period
次要结局
- severity of nausea(post-op period)
研究者
研究点 (1)
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