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临床试验/NCT01017380
NCT01017380已完成3 期

Comparing Etoricoxib and Celecoxib for Preemptive Analgesia for Acute Postoperative Pain in Patients Undergoing Arthroscopic Anterior Cruciate Ligament Reconstruction: A Randomized Controlled Trial

Prince of Songkla University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
30
试验地点
1
主要终点
VAS score

研究概览

简要总结

The aims of this study was to compare analgesic efficacy of preoperative administration of etoricoxib versus celecoxib for post-operative pain relief after arthroscopic anterior cruciate ligament reconstruction. One hundred and two patients diagnosed as anterior cruciate ligament injury will randomized into 3 groups using opaque envelope. Both patients and surgeon were blinded to the allocation. All of the patients will be operated by one orthopaedic surgeon under regional anesthesia. Each group will be given either etoricoxib 120 mg., celecoxib 400 mg., or placebo 1 hour prior to operative incision. Post-operative pain intensity, time to first dose of analgesic requirement and numbers of analgesic used for rescue pain control and adverse events will be recorded periodically to 48 hours after 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 (Participant, Outcomes Assessor)

入排标准

年龄范围
15 Years 至 50 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • patients with anterior cruciate ligament injury age 15-50 yr

排除标准

  • previous knee surgery

研究组 & 干预措施

placebo

Experimental

identical placebo

干预措施: Celecoxib (Drug)

placebo

Experimental

identical placebo

干预措施: etoricoxib (Drug)

结局指标

主要结局

VAS score

时间窗: 6,12,24,48 hour postoperative

次要结局

  • number of analgesic used(48 hour postoperative)

研究者

申办方类型
Other

研究点 (1)

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