Effect of Femoral Nerve Block on Opioid Requirements Following Anterior Cruciate Ligament Reconstruction: A Double Blind, Prospective Randomized Controlled Trial

University of British Columbia1 个研究点分布在 1 个国家目标入组 30 人开始时间: 2010年12月1日最近更新: 2016年6月1日

适应症

试验速览

阶段: 1 期
发起方: University of British Columbia
入组人数: 30
试验地点: 1
主要终点: Postoperative morphine requirement

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study evaluates the effect of a femoral nerve block on opioid requirements following anterior cruciate ligament (ACL) reconstruction. This is a double blind, prospective randomized controlled trial.

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: 12 Years 至 17 Years（Child）
性别: All
接受健康志愿者: 否

入选标准

•Schedule for primary elective anterior cruciate ligament reconstruction
•Tolerance to bupivacaine
•Tolerance to non-steroidal anti-inflammatory drugs (NSAIDs)
•Informed consent

排除标准

•Patients who received a femoral nerve block more than 1 hour prior to surgery
•Complex associated injuries or pre-existing conditions that will delay time to ambulation
•Children with tibial avulsion fractures
•Allergic and/or sensitive to bupivacaine and/or NSAIDs
•30% over ideal body weight
•Acute ACL reconstruction (done less than 2 weeks after injury)
•Pre-existing femoral nerve injury
•Psychiatric patients on psychotropic agents
•History of drug or alcohol dependence or recreational drug use
•Refusal to provide informed consent

结局指标

主要结局

Postoperative morphine requirement

次要结局

Pain rating(immediately post-op)
Opioid surgical time(time from end of anaesthesia to first requirement of morphine)

研究者

发起方

University of British Columbia

申办方类型

Other

责任方

Sponsor

研究点 (1)

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