跳至主要内容
临床试验/NCT00910013
NCT00910013已完成1 期

A Randomized Trial Comparing the Efficacy on Post-operative Analgesia of Intra-articular Ropivacaine Added to a Femoral Block After Total Knee Replacement

Hopital de l'Enfant-Jesus1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2006年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
80
试验地点
1
主要终点
Narcotic consumption per 24 hours after surgery (mg/kg)

研究概览

简要总结

Total knee replacement is a painful procedure. Many solutions have been proposed to diminish the post-operative doses of narcotics, including nerve blocks.

The purpose of the study is to compare if the adjunction of intra-articular ropivacaine to a femoral block is more effective on narcotics consumption than the block alone after TKR.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Primary total knee replacement
  • Age > 18 years old
  • Accept the study

排除标准

  • Revision surgery
  • Use of anticoagulants drugs
  • Neurologic disorder
  • Unable to sign consent form

研究组 & 干预措施

Ropivacaine + femoral block

Experimental

After the surgery is proceeded and after the closure of the joint capsule, 20 cc of ropivacaine 0.5% is inserted intra-articular through a catheter.

干预措施: Ropivacaine (Drug)

结局指标

主要结局

Narcotic consumption per 24 hours after surgery (mg/kg)

时间窗: 48 hours

次要结局

  • VAS score at 24 hours(48 hours)

研究者

发起方
Hopital de l'Enfant-Jesus
申办方类型
Other

研究点 (1)

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